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NCT02236026 · ClinicalTrials.gov registry record · Phase 1
A Study With an Open-Label Active Control to Evaluate the Potential of Nestorone® to Delay Cardiac Repolarization in Healthy Female Volunteers
A Phase 1 study, sponsored by Population Council.
- Completed
- Registry status
- Phase 1
- Development phase
- 44
- Enrollment target
NCT02236026: Completed Phase 1 study, sponsored by Population Council.
NCT02236026 is a Phase 1 study that has completed, run by Population Council. The registered enrollment target is 44 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02236026, a Phase 1 study, has completed, sponsored by Population Council.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 44 participants
- Enrollment target
Study Summary
The purpose of the study is to evaluate the effect of Nestorone (NES) administered as an bolus injection on the corrected QT interval using Fridericia's formula (QTcF).
Primary Outcome
Measurement of any changes from baseline in heart rhythm using an electrocardiogram at different time points after receiving NES as an IV solution
Interventions
- DRUG Placebo
- DRUG Moxifloxacin
- DRUG Supratherapuetic dose of Nestorone
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2014-09 |
| Est. Completion | 2015-12 |
| Phase | Phase 1 |
What the finished NCT02236026 record still lists
NCT02236026 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 44 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (27% lower).
The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.
NCT02236026 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02236026 about?
NCT02236026 is a clinical study titled "A Study With an Open-Label Active Control to Evaluate the Potential of Nestorone® to Delay Cardiac Repolarization in Healthy Female Volunteers". The purpose of the study is to evaluate the effect of Nestorone (NES) administered as an bolus injection on the corrected QT interval using Fridericia's formula (QTcF).
What is the current status of trial NCT02236026?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 44 participants. The study started on 2014-09. Estimated completion is 2015-12.
What interventions are being tested in trial NCT02236026?
The interventions under investigation include: Placebo (DRUG), Moxifloxacin (DRUG), Supratherapuetic dose of Nestorone (DRUG).
Who is sponsoring clinical trial NCT02236026?
This trial is sponsored by Population Council, which has 11 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02236026's enrollment target sits among peer trials
44 1086th of 2000 higher than 901 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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