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NCT02470741 · ClinicalTrials.gov registry record · Phase 4

Pilot of Letrozole for Uterine Myomas

A Phase 4 study, sponsored by University of California, San Francisco.

Completed
Registry status
Phase 4
Development phase
12
Enrollment target

NCT02470741: Completed Phase 4 study, sponsored by University of California, San Francisco.

NCT02470741 is a Phase 4 study that has completed, run by University of California, San Francisco. The registered enrollment target is 12 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02470741, a Phase 4 study, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
Phase 4
Development phase
12 participants
Enrollment target

Study Summary

PLUM evaluates the drug letrozole as a treatment for uterine fibroids. This study is a randomized, blinded, placebo-controlled trial of oral letrozole among premenopausal women with symptomatic uterine fibroids. Participants will be randomly assigned in a 1:1 ratio to either oral letrozole 2.5mg/day for 6 months (Group A) or intermittent dosing with letrozole 2.5mg/day and an identical placebo capsule (Group B).

Primary Outcome

The Uterine Fibroid Sympton and Quality of Life (UFS-QoL) Symptom Severity score measures self-reported severity of fibroid-related symptoms. Symptoms include: fatigue, sleep, self-image, mood disturbances/psychologic distress, fear of embarrassment, interference with daily activities, relationships with family and friends, and sexual functioning. Scores range from 0 to 100; higher scores indicate greater symptom severity.

Interventions

  • OTHER Placebo
  • DRUG Letrozole

Trial Details

FieldValue
Enrollment Target 12 participants
Start Date 2015-07
Est. Completion 2017-12
Phase Phase 4

What the finished NCT02470741 record still lists

NCT02470741 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02470741 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02470741 about?

NCT02470741 is a clinical study titled "Pilot of Letrozole for Uterine Myomas". PLUM evaluates the drug letrozole as a treatment for uterine fibroids. This study is a randomized, blinded, placebo-controlled trial of oral letrozole among premenopausal women with symptomatic uterine fibroids. Participants will be randomly assigned in a 1:1 ratio to either oral letrozole 2.5mg/day...

What is the current status of trial NCT02470741?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 12 participants. The study started on 2015-07. Estimated completion is 2017-12.

What interventions are being tested in trial NCT02470741?

The interventions under investigation include: Placebo (OTHER), Letrozole (DRUG).

Who is sponsoring clinical trial NCT02470741?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02470741's enrollment target sits among peer trials

12 1913th of 2000 higher than 70 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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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Source: ClinicalTrials.gov NCT02470741, the US trial registry maintained by the National Library of Medicine. NCT02470741 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.