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NCT00334048 · ClinicalTrials.gov registry record · Phase 4
Treating Sexual Dysfunction From Selective Serotonin Reuptake Inhibitor (SSRI) Medication: a Study Comparing Requip CR to Placebo
A Phase 4 study of Sexual Dysfunction, sponsored by St. Luke's-Roosevelt Hospital Center.
- Completed
- Registry status
- Phase 4
- Development phase
- 9
- Enrollment target
- 1
- Study location
NCT00334048 is a Phase 4 study of Sexual Dysfunction that has completed, run by St. Luke's-Roosevelt Hospital Center. The registered enrollment target is 9 participants, below the 967-participant average among 20 other Sexual Dysfunction trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT00334048, a Phase 4 study of Sexual Dysfunction, has completed, sponsored by St. Luke's-Roosevelt Hospital Center.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 9 participants
- Enrollment target
- 1
- Study location
Study Summary
Antidepressant medicines sometimes cause sexual side effects. The purpose of this study is to determine whether the sexual dysfunction sometimes caused by selective serotonin reuptake inhibitor (SSRI) antidepressant medications can be reversed by treatment with Requip (ropinirole), a medicine which is used to treat Parkinson's Disease and restless leg syndrome.
Conditions Studied
Interventions
- DRUG Ropinirole (Requip)
Study Locations (1)
New York
- Mood Disorders Research Program - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 9 participants |
| Start Date | 2006-06 |
| Est. Completion | 2007-09 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00334048
The ClinicalTrials.gov registry entry for NCT00334048 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 9 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 967-participant average among 20 other Sexual Dysfunction trials with a reported enrollment target (99% lower). The listed sponsor is St. Luke's-Roosevelt Hospital Center, which has 57 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Sexual Dysfunction appearing as the primary indexed condition, and to 1 intervention - of which Ropinirole (Requip) is the first listed.
NCT00334048 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT00334048 about?
NCT00334048 is a clinical study titled "Treating Sexual Dysfunction From Selective Serotonin Reuptake Inhibitor (SSRI) Medication: a Study Comparing Requip CR to Placebo". Antidepressant medicines sometimes cause sexual side effects. The purpose of this study is to determine whether the sexual dysfunction sometimes caused by selective serotonin reuptake inhibitor (SSRI) antidepressant medications can be reversed by treatment with Requip (ropinirole), a medicine which ...
What is the current status of trial NCT00334048?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 9 participants. The study started on 2006-06. Estimated completion is 2007-09.
What conditions does trial NCT00334048 study?
This clinical trial studies the following conditions: Sexual Dysfunction.
What interventions are being tested in trial NCT00334048?
The interventions under investigation include: Ropinirole (Requip) (DRUG).
Who is sponsoring clinical trial NCT00334048?
This trial is sponsored by St. Luke's-Roosevelt Hospital Center, which has 57 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00334048 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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