Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00937378 · ClinicalTrials.gov registry record · Phase 3
Treatment of Patients With Nocturia (Non-PK Study)
A Phase 3 study, sponsored by Serenity Pharmaceuticals.
- Completed
- Registry status
- Phase 3
- Development phase
- 326
- Enrollment target
NCT00937378: Completed Phase 3 study, sponsored by Serenity Pharmaceuticals.
NCT00937378 is a Phase 3 study that has completed, run by Serenity Pharmaceuticals. The registered enrollment target is 326 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00937378, a Phase 3 study, has completed, sponsored by Serenity Pharmaceuticals.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 326 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate a treatment of nocturia. The hypothesis is that SER120 will decrease the number of nocturic episodes compared to placebo.
Primary Outcome
Change was calculated as the mean number of nocturic episodes per night between baseline and Week 7
Interventions
- DRUG Placebo
- DRUG SER120
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 326 participants |
| Start Date | 2009-06 |
| Est. Completion | 2010-08 |
| Phase | Phase 3 |
What the finished NCT00937378 record still lists
NCT00937378 is an interventional study that assigns participants to a tested intervention. The registered 326 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (58% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT00937378 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00937378 about?
NCT00937378 is a clinical study titled "Treatment of Patients With Nocturia (Non-PK Study)". The purpose of this study is to evaluate a treatment of nocturia. The hypothesis is that SER120 will decrease the number of nocturic episodes compared to placebo.
What is the current status of trial NCT00937378?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 326 participants. The study started on 2009-06. Estimated completion is 2010-08.
What interventions are being tested in trial NCT00937378?
The interventions under investigation include: Placebo (DRUG), SER120 (DRUG).
Who is sponsoring clinical trial NCT00937378?
This trial is sponsored by Serenity Pharmaceuticals, which has 6 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00937378's enrollment target sits among peer trials
326 1075th of 2000 higher than 925 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 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
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT06410144 · 326 participants · NA
Chronic Kidney Disease-Education (CKD-EDU)
- NCT06586619 · 326 participants · NA
A Remotely Delivered Tai Chi/Qigong Intervention for Older People Living With HIV
- NCT07040566 · 326 participants · Phase 2
A Trial of Varenicline for E-cigarette Cessation
- NCT07165860 · 326 participants · NA
Clinical Trial to Reduce Perinatal Intimate Partner Violence
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia