Study setting {9}
The study will take place in 3 primary care HIV healthcare clinics and 1 wellness center of the AIDS Healthcare Foundation in Los Angeles and Oakland, California. Healthcare clinics offer HIV and sexually transmitted infection (STI) primary care services while wellness centers are walk-in comprehensive sexual health clinics that offer HIV/STI screening services, STI treatment and other prevention services.
Eligibility criteria {10}
The inclusion criteria are:
- Clinically or laboratory confirmed new cases of early syphilis (primary, secondary, early latent syphilis) with a plasma Rapid Plasma Reagin (RPR) ≥ 1:8
- 18 years of age or older, capable of providing informed consent
- HIV infected individuals must have CD4 T cll count≥350 cells/mm3 and be virologically suppressed (viral load < 200 copies/mL) during the past 6 months
- Able to travel to clinic once a day or be available for phone calls or receive text message for at least 7-10 days
The exclusion criteria are:
- Allergy to cefixime or penicillin
- Pregnancy or a positive pregnancy test
- Serofast RPR titer (prior titer ≥1:8 without history of 4-fold titer decline)
- Recent (within the past 7 days) or concomitant antimicrobial therapy with activity against syphilis, namely azithromycin, doxycycline, ceftriaxone or other beta lactam antibiotics (e.g. amoxicillin)
- A medical condition or other factor that might affect their ability to follow the protocol
Who will take informed consent? {26a}
Patients must provide written, informed consent before any study procedures occur (randomization, blood sample collection, treatment). Consent will be obtained by a study clinician in a private examination room. The clinician will explain the study goal, research procedures, participant rights and obligations following the informed consent sheet. The participant will be able to ask questions and will be given adequate time to review the consent and decide if they wish to participate. After reading through the document, the participant will provide their signature if they would like to take part in the study.
Additional consent provisions for collection and use of participant data and biological specimens {26b}
Patients will also sign a Health Insurance Portability and Accountability Act (HIPAA) release form allowing access to clinical and laboratory data, including their HIV test results.
Interventions
Explanation for the choice of comparators {6b}
This is a pilot, non-comparative clinical trial designed to collect preliminary efficacy data. It includes an “experimental arm” of participants receiving cefixime and a contemporaneous “control arm” of participants receiving benzathine penicillin. The study was not designed to be adequately powered to show a statistically significant difference in the efficacy between the penicillin and cefixime arms.
Intervention description {11a}
Eligible participants who provide their consent are randomized to the two arms of the study. Initially, the study team collects demographic (age, gender, race, ethnicity, contact, sexual orientation) and clinical information (most recent RPR titer, CD4 T cell count, HIV viral load). A venipuncture blood sample is collected by trained clinic staff and it is sent to the laboratory for testing. Testing is conducted on serum using the Arlington scientific RPR test kit (Arlington, Virginia) (22). Participants are randomly assigned to the two treatment groups. Participants assigned to the penicillin arm will receive 1 dose of 2.4M IU benzathine penicillin G on the day of enrollment. Participants who are assigned to the cefixime arm will be given 20 capsules of oral cefixime 400mg on the day of enrollment to take for the following 10 days. Study staff observed receipt of the first dose. Subjects in the cefixime arm will then be asked to return for a clinical assessment or have a phone call assessment with the study team member 2 weeks following enrolment.
Study staff will follow up with all participants at 3, 6, and 12 months. In each follow up, participants are asked questions regarding symptoms, antibiotic use in the past 3 months and number of sex partners with whom they had condom-less sex in the past 3 months. A new venipuncture blood sample is also collected for RPR testing
Criteria for discontinuing or modifying allocated interventions {11b}
Participants may request to leave the study or they may be withdrawn due to study-related adverse events. If a subject is discontinued from study participation due to an adverse event, they will be evaluated by the study clinicians for the need of additional treatment for syphilis. Safety data will be collected on any subject who is withdrawn from the study.
Participants in both study groups may receive additional treatment with penicillin, if they show no response to treatment (stable or absence of 4-fold decline at 6 months).
Strategies to improve adherence to interventions {11c}
To ensure retention of participants, follow-up visits will be scheduled to coincide with routine clinic appointments for HIV care or preventive sexual health appointments, which occur every three months. In addition, study staff will contact participants, either over the phone or via text message, before their scheduled follow-up appointment. Finally, participants will receive reimbursement for their time and transportation in the form of a gift card.
Relevant concomitant care permitted or prohibited during the trial {11d}
Usual HIV care and treatment for the participant will continue throughout the trial. Concomitant antibiotic use during the participation in the study duration of the trial will be recorded.
Provisions for post-trial care {30}
Once participants complete the study, they will be able to continue receiving clinical care from the clinics. Participants study records will be reviewed and if necessary, additional treatment for syphilis will be administered according to the standard of care protocol.
Outcomes {12}
The primary outcome is the successful treatment of early syphilis by the 3-, or 6-month follow-up. The participants’ RPR titer will be used as the primary measure of outcome. Successful treatment is defined as an equal or greater than 4-fold RPR titer decrease, from baseline to 3 or 6 months after treatment.
Participant timeline {13}
Participants will be part of the study for 12 months. Study evaluations will occur at 3, 6- and 12-months post-treatment. See Figure 1 for the participant timeline for the trial and Table 1 for the study assessments.
Sample size {14}
The primary outcome of the study will calculate the proportion of subjects with a 4-fold or greater decrease in RPR titer from baseline at 3 or 6 months in the per protocol analysis population
Assuming treatment success ratio of 90% among participants receiving cefixime, a sample size of 40 participants will yield a 95% confidence interval of (76% - 97%) (Table 2). Assuming 20% attrition due to loss to follow-up or non-compliance with study medication schedule enrolling 50 subjects will provide 40 evaluable subjects in the PP analysis population. Similarly, we will enroll 50 participants into the penicillin arm, as a contemporary cohort.
Recruitment {15}
Participant recruitment will occur in 4 AIDS Healthcare Foundation (AHF) Clinics based in Los Angeles, California and Oakland, California. During the scheduled clinical visit, the study clinicians will approach cases of syphilis returning for treatment and they will provide a brief overview of the study. If the participant is interested, the clinician will determine patient eligibility. If the patient is eligible and agrees to participate, the clinician will conduct the informed consent and enrollment. Participants will be able to discuss study details with the clinicians and ask questions before signing the informed consent. Following enrollment, participants will be randomized, do their laboratory test and receive the assigned treatment. Enrollment will be conducted by clinicians, who will be trained on the study procedures, and research assistants, who will assist in data collection, form preparation.
Assignment of interventions: randomization
Sequence generation {16a}
After consent, participants are randomly assigned to the study arms with a 1:1 allocation. We will use a simple randomization method with a shuffled deck of sealed envelopes that contain a card with the assigned treatment. One hundred randomization cards, 50 for each study group, will be created before the initiation of enrollment, sealed in unmarked envelopes and they will be distributed randomly to each of the study sites. No other factors will be taken into consideration for randomization.
Concealment mechanism {16b}
The envelopes containing the randomization cards are sealed, thus the team member conducting enrollment does not know the content of the envelope.
Implementation {16c}
The study staff will ask the participant to select a sealed envelope from the shuffled deck. After selecting the envelope, the participant will reveal the treatment to themselves and the study staff.
Assignment of interventions: Blinding
Who will be blinded {17a}
This is an open label clinical trial, thus neither the participants nor the study staff will be blinded to the assigned treatment. The data analyst performing interim and final statistical analyses will be masked to treatment assignment.
Procedure for unblinding if needed {17b}
Not applicable.
Data collection and management
Plans for assessment and collection of outcomes {18a}
A venipuncture blood sample will be collected at 3, 6, and 12 month visits and it will be tested for RPR titer.. Study data collected on baseline include basic demographic information, sexual history, laboratory tests (CD4 count, viral load, RPR titer). On each follow up visit, sexual history, antibiotic use, symptoms and the RPR titer will be collected. Data will be collected on paper data collection forms and will be entered into Research Electronic Data Capture (REDCap) (23, 24). The paper data collection forms were specifically designed for our study by the study research team to capture data relevant to our objective. Data quality and completeness is ensured through a weekly internal review process in which the research assistants review all data collection forms for completeness and the database for missing information.
Plans to promote participant retention and complete follow-up {18b}
Study follow-up visits are scheduled to coincide with routine clinic appointments within AHF. Study staff will send participants a 1 month, 2 week, and 1 day notification prior to their follow-up appointment.
Data management {19}
Participant data will be collected on paper data collection forms and entered into RedCap. Data that will be entered into RedCap include participant information (name, date of birth, medical record number, contact information) and laboratory results.
Confidentiality {27}
Redcap servers are encrypted, HIPAA-compliant, password protected and accessible only by designated study members. Hard copy data collection forms will be stored into a locked cabinet with limited access only to designated members.
Plans for collection, laboratory evaluation and storage of biological specimens for genetic or molecular analysis in this trial/future use {33}
Participants will provide a serum sample on baseline and at each follow up visit. Samples will be collected by trained laboratory personnel inside the clinics. Samples will be sent to the laboratory within 24 hours of collection. Sample processing and analysis will be conducted by trained laboratory staff following standard laboratory procedures. Samples will be destroyed after serological testing. The study team will not be involved in the sample collection, processing, analysis and reporting.
There are no plans in this trial to evaluate or store biological specimen for genetic or molecular analysis for future use.
Statistical methods
Statistical methods for primary and secondary outcomes {20a}
The primary analysis for the main outcome will be conducted on the “Per Protocol” (PP) population. This will include participants who satisfy the inclusion and exclusion criteria, completed treatment (i.e. received the penicillin injection or received all of the cefixime pills), report no adverse events, returned for follow-up visits (3 and/or 6 months) and have an evaluable RPR result.
For each treatment group, we will calculate the proportion of PP participants who achieved a 4-fold RPR titer decrease at 3, or 6-months post-treatment (“Treatment success”) and the exact binomial 95% confidence interval. Qualitative variables will be presented as frequencies with percentages and 95% confidence intervals (95%CIs) and quantitative variables as mean with standard deviation and range.
Methods for additional analyses (e.g. subgroup analyses) {20b}
There will be no other additional analyses beyond the main analyses for the primary and secondary outcomes.
Methods in analysis to handle protocol non-adherence and any statistical methods to handle missing data {20c}
Participants who don’t adherence to the protocol or participants with missing data will not be included in the primary outcome analysis. We will be conducting an “Intention to Treat” (ITT) analysis that will include all individuals enrolled in the study, with evaluable RPR titter results and regardless of protocol non-compliance. For this analysis, missing data and non-adherent cases will also be considered as ‘Treatment failure’. Similarly to the PP analysis, we will calculate the treatment success proportion for each treatment group among the ITT population at 3, or 6-months post-treatment and the exact binomial 95% confidence interval.
Interim analyses {21b}
A summary of the enrollment progress, treatment success proportions, adverse events and protocol deviations will be provided to the Data Safety Monitoring Board members.
Plans to give access to the full protocol, participant level-data and statistical code {31c}
The protocol of the study is publicly available on clinicaltrials.gov (NCT03660488). Deidentified data will be available upon request to the study Primary Investigator.
Oversight and monitoring
Composition of the coordinating center and trial steering committee {5d}
The immediate study research team based in the University of California of Los Angeles meets on a weekly basis and oversees study recruitment, data quality, and study staff trainings. The immediate team is joined by a wider team of AHF study clinicians, based in study clinics, who also meet on a weekly basis.
Composition of the data monitoring committee, its role and reporting structure {21a}
The Data and Safety Monitoring Board (DSMB) will be composed of a physician, biostatistician, regulatory affairs specialist/ethicist and will oversee the study throughout the 2-year study period. They will review study activities every 6 months. The committee will review safety data and clinical efficacy reports and determine whether it is clinically safe to continue the clinical trial. They will report their recommendation to the Primary investigator.
Adverse event reporting and harms {22}
Cefixime and penicillin have a known safety and adverse event profile. Participants receiving penicillin may experience temporary mild pain on the site of injection. Cefixime can cause mild gastrointestinal reactions, such as diarrhea, loose stools, abdominal pain and nausea14. Mild to severe allergic reactions are also expected in persons allergic to penicillin or cefixime.
Adverse events will be collected by spontaneous self-report. Study participants will be asked to report any problems throughout their participation to the study and specifically the duration of the treatment. We will use the Division of AIDS (DAIDS) Adverse Event grading system [https://rsc.niaid.nih.gov/clinical-research-sites/daids-adverse-event-grading-tables] that classifies adverse events by organ system and severity. Any AE/SAEs will be reported descriptively on the final project report and future publications.
The study site investigators will report serious adverse events and adverse events to the responsible IRB for that study site in accordance with respective IRB policies and procedures. Follow-up information to a reported adverse event will be submitted to the IRB as soon as the relevant information is available.
Frequency and plans for auditing trial conduct {23}
The trial and individual clinic sites will be audited at least once during the duration of the study by the study sponsor (AIDS Healthcare Foundation).
Plans for communicating important protocol amendments to relevant parties (e.g. trial participants, ethical committees) {25}
Amendments will be submitted to the IRB according to policies and guidance. Any protocol changes will be promptly communicated to the IRB, the DSMB and the study team.
Dissemination plans {31a}
We plan to disseminate study results through peer-reviewed journal publications and conference presentations. Study findings will also be shared with relevant clinical and scientific groups.