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NCT03038308 · ClinicalTrials.gov registry record · Phase 1
Treatment of Hyperprolactinemia With the Non-ergoline Dopamine Agonist Ropinirole
A Phase 1 study, sponsored by Columbia University.
- Completed
- Registry status
- Phase 1
- Development phase
- 16
- Enrollment target
NCT03038308: Completed Phase 1 study, sponsored by Columbia University.
NCT03038308 is a Phase 1 study that has completed, run by Columbia University. The registered enrollment target is 16 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03038308, a Phase 1 study, has completed, sponsored by Columbia University.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 16 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the use of the non-ergoline dopamine agonist ropinirole for the treatment of hyperprolactinemia in patients with idiopathic hyperprolactinemia and prolactinomas.
Primary Outcome
Serum prolactin concentrations (PRL levels) were measured in patients at baseline, 2 and 4 weeks after starting therapy and then once monthly thereafter for 24 weeks. Serum prolactin was measured in duplicate by two-site chemiluminescent enzyme immunometric assay using the Immulite 1000 Analyzer (Siemens Healthcare Diagnostics, Deerfield, IL). The reference range for serum prolactin is 1.9-25 ng/ml for adult females.
Interventions
- DRUG Ropinirole
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 16 participants |
| Start Date | 2016-09-16 |
| Est. Completion | 2020-11-05 |
| Phase | Phase 1 |
What the finished NCT03038308 record still lists
NCT03038308 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 16 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (73% lower).
The record links to 0 conditions, and to 1 intervention - of which Ropinirole is the first listed.
NCT03038308 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03038308 about?
NCT03038308 is a clinical study titled "Treatment of Hyperprolactinemia With the Non-ergoline Dopamine Agonist Ropinirole". The purpose of this study is to evaluate the use of the non-ergoline dopamine agonist ropinirole for the treatment of hyperprolactinemia in patients with idiopathic hyperprolactinemia and prolactinomas.
What is the current status of trial NCT03038308?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 16 participants. The study started on 2016-09-16. Estimated completion is 2020-11-05.
What interventions are being tested in trial NCT03038308?
The interventions under investigation include: Ropinirole (DRUG).
Who is sponsoring clinical trial NCT03038308?
This trial is sponsored by Columbia University, which has 958 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03038308's enrollment target sits among peer trials
16 1786th of 2000 higher than 203 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 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
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