Urogenital Chlamydia trachomatis infection Infections and Infestations Other sexually transmitted chlamydial diseases
Conditions
Interventions
A single-centre randomized controlled trial among urogenital chlamydia nucleic acid amplification test positive heterosexual Amsterdam STI clinic clients. After treatment, patients were randomly assig
Sponsors
Public Health Service
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Heterosexual patients of the Amsterdam STI clinic testing positive for urogenital chlamydia 2. Aged 12 years or older
Exclusion criteria
Exclusion criteria: Does not meet inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. The number and percentage of participants retested up to 35 weeks after inclusion 2. The proportion of participants who were CT positive, measured by nucleic acid amplification test, up to 35 weeks after inclusion | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. The number, percentage and chlamydia positivity proportion of participants who: 1.1. Returned more than 1 week before the assigned date 1.2. Returned at assigned date (this was defined as a visit in the period >1 week before, until 6 weeks after the assigned date) 1.3. Returned >6 weeks after the assigned date but no later than 35 weeks (8 months) after inclusion 1.4. Those who did not return within 35 weeks of inclusion | — |
Countries
Netherlands
Outcome results
None listed