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NCT00656201 · ClinicalTrials.gov registry record · Phase 4
Comparison of Crinone 8% Intravaginal Gel and IM Progesterone Supplementation for In Vitro Fertilization (IVF)
A Phase 4 study, sponsored by Brigham and Women's Hospital.
- Completed
- Registry status
- Phase 4
- Development phase
- 468
- Enrollment target
NCT00656201 is a Phase 4 study that has completed, run by Brigham and Women's Hospital. The registered enrollment target is 468 participants.
The verdict
NCT00656201, a Phase 4 study, has completed, sponsored by Brigham and Women's Hospital.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 468 participants
- Enrollment target
Study Summary
The goal of this research study is to compare the pregnancy rates for two different types of progesterone supplementation after in-vitro fertilization (IVF).
Interventions
- DRUG Intramuscular Progesterone
- DRUG Crinone 8% Vaginal Gel
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 468 participants |
| Start Date | 2003-07 |
| Est. Completion | 2009-07 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00656201
The ClinicalTrials.gov registry entry for NCT00656201 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 468 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Brigham and Women's Hospital, which has 937 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Intramuscular Progesterone is the first listed.
NCT00656201 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00656201 about?
NCT00656201 is a clinical study titled "Comparison of Crinone 8% Intravaginal Gel and IM Progesterone Supplementation for In Vitro Fertilization (IVF)". The goal of this research study is to compare the pregnancy rates for two different types of progesterone supplementation after in-vitro fertilization (IVF).
What is the current status of trial NCT00656201?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 468 participants. The study started on 2003-07. Estimated completion is 2009-07.
What interventions are being tested in trial NCT00656201?
The interventions under investigation include: Intramuscular Progesterone (DRUG), Crinone 8% Vaginal Gel (DRUG).
Who is sponsoring clinical trial NCT00656201?
This trial is sponsored by Brigham and Women's Hospital, which has 937 total clinical trials registered on ClinicalTrials.gov.
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