Table 1 Study assessments by study time point
From: Clinical trial protocol to evaluate the efficacy of cefixime in the treatment of early syphilis
Assessment | Time point | ||||
|---|---|---|---|---|---|
Enrolment | 10-day follow-up (cefixime arm only) | 3-month visit | 6-month visit | 12-month visit | |
Eligibility screening | X | ||||
Consent | X | ||||
Randomization | X | ||||
Demographic information | X | ||||
Clinical & laboratory information | X | ||||
Blood sample collection (RPR and RPR titer) | X | X | X | X | |
Treatment administration | X | ||||
Evaluation of treatment completion | X | ||||
Recent sexual history | X | X | X | X | X |
Recent antibiotic use | X | X | X | X | X |