Chlamydia detection after treatment in persons attending an STI clinic

Completed

• Conditions: Chlamydia; Sexually transmitted infection; 10008555

• Registration Number: NL-OMON42048
• Lead Sponsor: Medisch Universitair Ziekenhuis Maastricht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 600

Inclusion Criteria

Participants include symptomatic and asymptomatic genital and/or anorectal CT positive women and males who are their sex partners at inclusion.

Exclusion Criteria

Women who:
recently (last month) use antibiotics
were positive for HIV and / of Neisseria gonorrhoeae (NG)
are pregnant
<18 years

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The outcome is detection of anorectal and genital CT at any of the time<br /><br>-points. Primary outcome is detection by NAAT. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary outcomes include detection of viable CT, CT-DNA concentration,<br /><br>proportion of observed reticulate/elementary bodies, and CT genotype<br /><br>concordance.</p><br>