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NCT02462954 · ClinicalTrials.gov registry record · Phase 1
A Safety Study Of The Caya® Diaphragm Used With ContraGel®
A Phase 1 study, sponsored by CONRAD.
- Completed
- Registry status
- Phase 1
- Development phase
- 23
- Enrollment target
NCT02462954: Completed Phase 1 study, sponsored by CONRAD.
NCT02462954 is a Phase 1 study that has completed, run by CONRAD. The registered enrollment target is 23 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02462954, a Phase 1 study, has completed, sponsored by CONRAD.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 23 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety of ContraGel versus the hydroxyethylcellulose (HEC) Universal Placebo gel when used with the Caya diaphragm during two 7-day periods of daily use, the first without intercourse and the second with intercourse.
Interventions
- DEVICE ContraGel
- DEVICE HEC Universal Placebo gel
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2015-07 |
| Est. Completion | 2016-04 |
| Phase | Phase 1 |
What the finished NCT02462954 record still lists
NCT02462954 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 23 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (62% lower).
The record links to 0 conditions, and to 2 interventions - of which ContraGel is the first listed.
NCT02462954 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02462954 about?
NCT02462954 is a clinical study titled "A Safety Study Of The Caya® Diaphragm Used With ContraGel®". The purpose of this study is to evaluate the safety of ContraGel versus the hydroxyethylcellulose (HEC) Universal Placebo gel when used with the Caya diaphragm during two 7-day periods of daily use, the first without intercourse and the second with intercourse.
What is the current status of trial NCT02462954?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2015-07. Estimated completion is 2016-04.
What interventions are being tested in trial NCT02462954?
The interventions under investigation include: ContraGel (DEVICE), HEC Universal Placebo gel (DEVICE).
Who is sponsoring clinical trial NCT02462954?
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 NCT02462954's enrollment target sits among peer trials
23 1596th of 2000 higher than 400 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 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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