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NCT00951171 · ClinicalTrials.gov registry record · Phase 3
Effect of Cervical Occlusion During Intrauterine Insemination (IUI)
A Phase 3 study, sponsored by Women and Infants Hospital of Rhode Island.
- Terminated
- Registry status
- Phase 3
- Development phase
- 93
- Enrollment target
NCT00951171 is a Phase 3 study that was terminated before completion, run by Women and Infants Hospital of Rhode Island. The registered enrollment target is 93 participants.
The verdict
NCT00951171, a Phase 3 study, was terminated before completion, sponsored by Women and Infants Hospital of Rhode Island.
- TERMINATED
- Registry status
- Phase 3
- Development phase
- 93 participants
- Enrollment target
Study Summary
Study Hypothesis: There is a difference in pregnancy rates between intrauterine insemination (IUI) in cycles performed with cervical occlusion by a balloon catheter designed for sonohysterograms as compared to those performed with a standard inseminator. The investigators will compare pregnancy rates in patients undergoing routine IUI either with balloon occlusion or with standard insemination. The patients will receive the standard clinical care per the investigators' office guidelines, except they will be randomized to insemination with either of two catheters.
Interventions
- PROCEDURE Intrauterine Insemination
- PROCEDURE IUI with the standard inseminator
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 93 participants |
| Start Date | 2009-02 |
| Est. Completion | 2011-12 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00951171
The ClinicalTrials.gov registry entry for NCT00951171 describes a study currently listed as terminated, categorized as Phase 3. The registered enrollment target is 93 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Women and Infants Hospital of Rhode Island, which has 65 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Intrauterine Insemination is the first listed.
NCT00951171 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00951171 about?
NCT00951171 is a clinical study titled "Effect of Cervical Occlusion During Intrauterine Insemination (IUI)". Study Hypothesis: There is a difference in pregnancy rates between intrauterine insemination (IUI) in cycles performed with cervical occlusion by a balloon catheter designed for sonohysterograms as compared to those performed with a standard inseminator. The investigators will compare pregnancy rat...
What is the current status of trial NCT00951171?
This trial is currently terminated. It is a Phase 3 study. The enrollment target is 93 participants. The study started on 2009-02. Estimated completion is 2011-12.
What interventions are being tested in trial NCT00951171?
The interventions under investigation include: Intrauterine Insemination (PROCEDURE), IUI with the standard inseminator (PROCEDURE).
Who is sponsoring clinical trial NCT00951171?
This trial is sponsored by Women and Infants Hospital of Rhode Island, which has 65 total clinical trials registered on ClinicalTrials.gov.
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