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NCT03815344 · ClinicalTrials.gov registry record · Phase 4

Combined Vaginal Misoprostol and Perivascular Vasopressin

A Phase 4 study, sponsored by Antonios Likourezos.

Completed
Registry status
Phase 4
Development phase
74
Enrollment target

NCT03815344: Completed Phase 4 study, sponsored by Antonios Likourezos.

NCT03815344 is a Phase 4 study that has completed, run by Antonios Likourezos. The registered enrollment target is 74 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03815344, a Phase 4 study, has completed, sponsored by Antonios Likourezos.

COMPLETED
Registry status
Phase 4
Development phase
74 participants
Enrollment target

Study Summary

Injection of Vasopressin into the uterine tissue surrounding fibroids constricts blood vessels, and has been found to be beneficial by decreasing blood flow to fibroids, and thereby resulting in less bleeding with removal. Additionally, Misoprostol has been looked at as an additional method to decrease operative blood loss given its ability to increase uterine muscle tone, which therefore constricts the amount of blood flow to the uterus.

Primary Outcome

The difference in hemoglobin levels between pre surgery and post surgery

Interventions

  • DRUG Standard
  • DRUG Standard-vaginal misoprostol

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2017-04-26
Est. Completion 2019-06-30
Phase Phase 4
Antonios Likourezos

33 total trials

What the finished NCT03815344 record still lists

NCT03815344 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (86% lower).

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

NCT03815344 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03815344 about?

NCT03815344 is a clinical study titled "Combined Vaginal Misoprostol and Perivascular Vasopressin". Injection of Vasopressin into the uterine tissue surrounding fibroids constricts blood vessels, and has been found to be beneficial by decreasing blood flow to fibroids, and thereby resulting in less bleeding with removal. Additionally, Misoprostol has been looked at as an additional method to decre...

What is the current status of trial NCT03815344?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 74 participants. The study started on 2017-04-26. Estimated completion is 2019-06-30.

What interventions are being tested in trial NCT03815344?

The interventions under investigation include: Standard (DRUG), Standard-vaginal misoprostol (DRUG).

Who is sponsoring clinical trial NCT03815344?

This trial is sponsored by Antonios Likourezos, which has 33 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03815344's enrollment target sits among peer trials

74 1027th of 2000 higher than 968 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 NCT03815344, the US trial registry maintained by the National Library of Medicine. NCT03815344 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.