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NCT00475189 · ClinicalTrials.gov registry record · NA
Study of Loestrin 24(24 Days of "Real" Pills) Fe Versus Loestrin 1/20 (21 "Real" Pills)
A NA study, sponsored by Scott and White Hospital & Clinic.
- Completed
- Registry status
- NA
- Development phase
- 51
- Enrollment target
NCT00475189 is a NA study that has completed, run by Scott and White Hospital & Clinic. The registered enrollment target is 51 participants.
The verdict
NCT00475189, a NA study, has completed, sponsored by Scott and White Hospital & Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 51 participants
- Enrollment target
Study Summary
The purpose of this research study is to assess hormone withdrawal symptoms in women while taking an oral contraceptive in the novel 24/4 (24 days of "real" pills) manner in comparison to taking pills in the standard 21/7 (21 "real" pills) manner. It is hypothesized that the 24/4 method will reduce common hormone withdrawal symptoms compared to the standard 21/7 regimen. It is further hypothesized that women using the 24/4 regimen will report greater satisfaction scores.
Interventions
- DRUG loestrin 24/4 vs loestrin 1/20
- DRUG loestrin 1/20
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 51 participants |
| Start Date | 2007-06 |
| Est. Completion | 2008-11 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00475189
The ClinicalTrials.gov registry entry for NCT00475189 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Scott and White Hospital & Clinic, which has 9 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which loestrin 24/4 vs loestrin 1/20 is the first listed.
NCT00475189 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00475189 about?
NCT00475189 is a clinical study titled "Study of Loestrin 24(24 Days of "Real" Pills) Fe Versus Loestrin 1/20 (21 "Real" Pills)". The purpose of this research study is to assess hormone withdrawal symptoms in women while taking an oral contraceptive in the novel 24/4 (24 days of "real" pills) manner in comparison to taking pills in the standard 21/7 (21 "real" pills) manner. It is hypothesized that the 24/4 method will reduce...
What is the current status of trial NCT00475189?
This trial is currently completed. It is a NA study. The enrollment target is 51 participants. The study started on 2007-06. Estimated completion is 2008-11.
What interventions are being tested in trial NCT00475189?
The interventions under investigation include: loestrin 24/4 vs loestrin 1/20 (DRUG), loestrin 1/20 (DRUG).
Who is sponsoring clinical trial NCT00475189?
This trial is sponsored by Scott and White Hospital & Clinic, which has 9 total clinical trials registered on ClinicalTrials.gov.
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