Gonorrhea Clinical Trials

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Evaluation of Performance, Acceptability, and Usability of a Novel Lateral Flow Assay for Point-of-Care Detection of Neisseria Gonorrhoeae Infection Among Pregnant and Symptomatic Women in South Africa

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

Previous studies of the Neisseria gonorrhoeae (NG) lateral flow assay (LFA) have shown promising results. In East London, South Africa, the LFA demonstrated a sensitivity of 80% in asymptomatic women. However, a study in Zimbabwe reported a lower sensitivity of 65% among pregnant women attending antenatal care (ANC). This discrepancy raises important questions about the test's performance in pregnant women in the East London ANC population. Physiological changes during pregnancy may influence test accuracy, highlighting the need for further investigation in this specific population and setting. This study aims to evaluate the performance, acceptability, and usability of the NG LFA among pregnant and symptomatic women attending clinics in East London. Participants will provide clinical samples that are tested using both the NG LFA and standard laboratory methods to assess diagnostic accuracy, including sensitivity and specificity. The study will specifically determine whether pregnancy affects the test's performance and whether the LFA is reliable for routine use in ANC clinics. Confirming its accuracy could enable wider implementation, improving case detection, treatment rates, and reducing the burden of gonorrhea in the community. In addition to evaluating performance, the study will investigate the feasibility of self-collected samples. Self-collection offers privacy, convenience, and may increase participation in testing, particularly for women who prefer this method. It may also reduce the workload for healthcare providers, especially in resource-limited settings. The study will compare the accuracy of self-collected samples with clinician-collected samples to determine whether self-collection is a viable option in ANC and symptomatic populations. The findings will provide crucial evidence to guide implementation of the NG LFA in primary care and ANC clinics, supporting timely diagnosis and treatment. If successful, this approach could strengthen gonorrhea screening programs, enhance patient-centered care, and contribute to better sexual and reproductive health outcomes for women in South Africa.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: t
View:

⁃ ANC population

• Women age ≥18 years

• Pregnant women

• Attending a study site for antenatal care

• Willingness to participate and signed informed consent form (ICF)

Locations
Other Locations
South Africa
1. Nontyatyambo CHC 2. Empilweni Gompo CHC 3. Duncan Village Day Hospital 4. Grey Gateway Clinic 5. Ndevana Clinic
RECRUITING
East London
Contact Information
Primary
Mandisa M Mdingi, Master of Public Health
mandisam@founadtion.co.za
+27 73 706 9068
Backup
Dr Sarita Naidoo, PhD
saritan@foundation.co.za
+27 (0) 12 110 4080
Time Frame
Start Date: 2025-09-11
Estimated Completion Date: 2026-06-30
Participants
Target number of participants: 1239
Treatments
Pregnant Women Cohort and Symptomatic Women Cohort
This is a cross-sectional, single time-point study with a paired design to determine the diagnostic accuracy of the NG LFA against the Xpert® CT/NG as a reference standard in vaginal samples collected from pregnant women attending ANC and to compare the accuracy and safety of self-collected and provider-collected samples in both non-pregnant symptomatic and pregnant ANC attendees.
Related Therapeutic Areas
Sponsors
Leads: Foundation for Professional Development (Pty) Ltd
Collaborators: Foundation for Innovative New Diagnostics, Switzerland

This content was sourced from clinicaltrials.gov