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NCT03057041 · ClinicalTrials.gov registry record · NA

Intranasal Fentanyl for Pain Control During First-Trimester Uterine Aspiration

A NA study, sponsored by University of Hawaii.

Completed
Registry status
NA
Development phase
107
Enrollment target

NCT03057041: Completed NA study, sponsored by University of Hawaii.

NCT03057041 is a NA study that has completed, run by University of Hawaii. The registered enrollment target is 107 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03057041, a NA study, has completed, sponsored by University of Hawaii.

COMPLETED
Registry status
NA
Development phase
107 participants
Enrollment target

Study Summary

Intranasal fentanyl has been found to be safe and effective in the reduction of pain among pediatric and adult populations. The investigators hypothesize that patients who receive 100 mcg of intranasal fentanyl for pain control before first-trimester uterine aspiration will report lower pain scores than those who receive placebo. The investigators will test this hypothesis using a randomized, double-blind, placebo-controlled trial comparing pain reported during uterine aspiration between patients who receive either intranasal fentanyl or intranasal saline prior to the procedure.

Primary Outcome

Self reported on 100 mm VAS

Interventions

  • DRUG placebo
  • DRUG Fentanyl

Trial Details

FieldValue
Enrollment Target 107 participants
Start Date 2017-03-23
Est. Completion 2018-05-30
Phase NA
University of Hawaii

77 total trials

What the finished NCT03057041 record still lists

NCT03057041 is an interventional study that assigns participants to a tested intervention. The registered 107 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).

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

NCT03057041 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03057041 about?

NCT03057041 is a clinical study titled "Intranasal Fentanyl for Pain Control During First-Trimester Uterine Aspiration". Intranasal fentanyl has been found to be safe and effective in the reduction of pain among pediatric and adult populations. The investigators hypothesize that patients who receive 100 mcg of intranasal fentanyl for pain control before first-trimester uterine aspiration will report lower pain scores ...

What is the current status of trial NCT03057041?

This trial is currently completed. It is a NA study. The enrollment target is 107 participants. The study started on 2017-03-23. Estimated completion is 2018-05-30.

What interventions are being tested in trial NCT03057041?

The interventions under investigation include: placebo (DRUG), Fentanyl (DRUG).

Who is sponsoring clinical trial NCT03057041?

This trial is sponsored by University of Hawaii, which has 77 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03057041's enrollment target sits among peer trials

107 830th of 2000 higher than 1,171 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT03057041, the US trial registry maintained by the National Library of Medicine. NCT03057041 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.