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NCT04177693 · ClinicalTrials.gov registry record · Phase 1
Pharmacokinetics and Hepatic Safety of EGCG
A Phase 1 study, sponsored by Yale University.
- Completed
- Registry status
- Phase 1
- Development phase
- 39
- Enrollment target
NCT04177693: Completed Phase 1 study, sponsored by Yale University.
NCT04177693 is a Phase 1 study that has completed, run by Yale University. The registered enrollment target is 39 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04177693, a Phase 1 study, has completed, sponsored by Yale University.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 39 participants
- Enrollment target
Study Summary
A trial to assess the pharmacokinetics and hepatic safety of EGCG in women with and without uterine fibroids.
Primary Outcome
Changes in epigallocatechin gallate (EGCG) from Visit 1 to Visit 4 (end of study). EGCG levels measured at 1 hour after taking study medication were used for both visits.
Interventions
- DRUG Letrozole
- DRUG Clomiphene Citrate
- DIETARY_SUPPLEMENT Epigallocatechin gallate (EGCG)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 39 participants |
| Start Date | 2020-11-24 |
| Est. Completion | 2022-01-31 |
| Phase | Phase 1 |
What the finished NCT04177693 record still lists
NCT04177693 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 39 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (35% lower).
The record links to 0 conditions, and to 3 interventions - of which Letrozole is the first listed.
NCT04177693 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04177693 about?
NCT04177693 is a clinical study titled "Pharmacokinetics and Hepatic Safety of EGCG". A trial to assess the pharmacokinetics and hepatic safety of EGCG in women with and without uterine fibroids.
What is the current status of trial NCT04177693?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 39 participants. The study started on 2020-11-24. Estimated completion is 2022-01-31.
What interventions are being tested in trial NCT04177693?
The interventions under investigation include: Letrozole (DRUG), Clomiphene Citrate (DRUG), Epigallocatechin gallate (EGCG) (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT04177693?
This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04177693's enrollment target sits among peer trials
39 1191st of 2000 higher than 804 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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