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NCT01593124 · ClinicalTrials.gov registry record · Phase 2
Identification of Novel Biomarkers of Cervicovaginal Mucosal Inflammation
A Phase 2 study, sponsored by CONRAD.
- Completed
- Registry status
- Phase 2
- Development phase
- 20
- Enrollment target
NCT01593124: Completed Phase 2 study, sponsored by CONRAD.
NCT01593124 is a Phase 2 study that has completed, run by CONRAD. The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01593124, a Phase 2 study, has completed, sponsored by CONRAD.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 20 participants
- Enrollment target
Study Summary
This study investigates the response of vaginal and cervical tissue after exposure to three vaginal products: hydroxyethyl cellulose (HEC) placebo, nonoxynol-9 (N9) and imiquimod (IMQ) cream.
Primary Outcome
These data are still undergoing analysis
Interventions
- OTHER Placebo
- DRUG Imiquimod
- DRUG Nonoxynol-9
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2012-05 |
| Est. Completion | 2013-04 |
| Phase | Phase 2 |
What the finished NCT01593124 record still lists
NCT01593124 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).
The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.
NCT01593124 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01593124 about?
NCT01593124 is a clinical study titled "Identification of Novel Biomarkers of Cervicovaginal Mucosal Inflammation". This study investigates the response of vaginal and cervical tissue after exposure to three vaginal products: hydroxyethyl cellulose (HEC) placebo, nonoxynol-9 (N9) and imiquimod (IMQ) cream.
What is the current status of trial NCT01593124?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2012-05. Estimated completion is 2013-04.
What interventions are being tested in trial NCT01593124?
The interventions under investigation include: Placebo (OTHER), Imiquimod (DRUG), Nonoxynol-9 (DRUG).
Who is sponsoring clinical trial NCT01593124?
This trial is sponsored by CONRAD, which has 33 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01593124's enrollment target sits among peer trials
20 1805th of 2000 higher than 107 of 2,000 other Phase 2 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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