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NCT03716739 · ClinicalTrials.gov registry record · Phase 2

Improving Quality of Life of Prostate Cancer Survivors With Androgen Deficiency

A Phase 2 study, sponsored by Dana-Farber Cancer Institute.

Completed
Registry status
Phase 2
Development phase
136
Enrollment target

NCT03716739: Completed Phase 2 study, sponsored by Dana-Farber Cancer Institute.

NCT03716739 is a Phase 2 study that has completed, run by Dana-Farber Cancer Institute. The registered enrollment target is 136 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03716739, a Phase 2 study, has completed, sponsored by Dana-Farber Cancer Institute.

COMPLETED
Registry status
Phase 2
Development phase
136 participants
Enrollment target

Study Summary

The purpose of this phase II trial is to determine the efficacy and safety of testosterone replacement therapy (TRT) in improving the symptoms of androgen deficiency and health-related quality of life in men with prostate cancer who have undergone radical prostatectomy.

Primary Outcome

The primary safety endpoint is the number of participants with biochemical recurrence of prostate cancer. Biochemical recurrence is defined as two or more consecutive serum PSA levels of 0.2 ng/mL or higher.

Interventions

  • DRUG Placebo
  • DRUG Testosterone Cypionate 100 MG/ML

Trial Details

FieldValue
Enrollment Target 136 participants
Start Date 2019-03-19
Est. Completion 2025-07-16
Phase Phase 2
Dana-Farber Cancer Institute

781 total trials

What the finished NCT03716739 record still lists

NCT03716739 is an interventional study that assigns participants to a tested intervention. The registered 136 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

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

NCT03716739 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03716739 about?

NCT03716739 is a clinical study titled "Improving Quality of Life of Prostate Cancer Survivors With Androgen Deficiency". The purpose of this phase II trial is to determine the efficacy and safety of testosterone replacement therapy (TRT) in improving the symptoms of androgen deficiency and health-related quality of life in men with prostate cancer who have undergone radical prostatectomy.

What is the current status of trial NCT03716739?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 136 participants. The study started on 2019-03-19. Estimated completion is 2025-07-16.

What interventions are being tested in trial NCT03716739?

The interventions under investigation include: Placebo (DRUG), Testosterone Cypionate 100 MG/ML (DRUG).

Who is sponsoring clinical trial NCT03716739?

This trial is sponsored by Dana-Farber Cancer Institute, which has 781 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03716739's enrollment target sits among peer trials

136 527th of 2000 higher than 1,469 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT03716739, the US trial registry maintained by the National Library of Medicine. NCT03716739 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.