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NCT04126824 · ClinicalTrials.gov registry record · Early Phase 1

Effect of Addition of Steroids on Duration of Analgesia

A Early Phase 1 study of Uterine Fibroids and Adenomyosis, sponsored by University of California, Los Angeles.

Active
Registry status
Early Phase 1
Development phase
28
Enrollment target
2
Study locations

NCT04126824: Active Early Phase 1 study of Uterine Fibroids and Adenomyosis, sponsored by University of California, Los Angeles.

NCT04126824 is a Early Phase 1 study of Uterine Fibroids and Adenomyosis that is active but no longer recruiting, run by University of California, Los Angeles. The registered enrollment target is 28 participants, below the 241-participant average among 10 other Uterine Fibroids trials with a reported enrollment target (88% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04126824, a Early Phase 1 study of Uterine Fibroids and Adenomyosis, is active but no longer recruiting, sponsored by University of California, Los Angeles.

ACTIVE NOT RECRUITING
Registry status
Early Phase 1
Development phase
28 participants
Enrollment target
2
Study locations

Study Summary

The purpose of the study is to investigate the differences in post-procedural pain scores and narcotic use among patients who receive a Superior Hypogastric Nerve Block (SHNB) with and without corticosteroid performed as part of the Uterine Artery Embolization (UAE) procedure.

Primary Outcome

The pain intensity is assessed using a visual analogue scale (VAS), which is a horizontal line 100 mm in length. Subjects mark the VAS with a single vertical line to indicate their current pain level, with 0 mm representing "No Pain" and 100 mm representing "Worst Possible Pain".

Interventions

  • DRUG Bupivacaine
  • DRUG Triamcinolone
  • OTHER Iohexol contrast

Study Locations (2)

California

  • University of California, Los Angeles - Westwood, Los Angeles

North Carolina

  • University of North Carolina - Chapel Hill

Trial Details

FieldValue
Enrollment Target 28 participants
Start Date 2022-01-06
Est. Completion 2027-08-02
Phase Early Phase 1

What the registry record for NCT04126824 still lists

NCT04126824 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 28 participants, a relatively small participant target, below the 241-participant average among 10 other Uterine Fibroids trials with a reported enrollment target (88% lower).

The record links to 2 conditions, with Uterine Fibroids appearing as the primary indexed condition, and to 3 interventions - of which Bupivacaine is the first listed.

NCT04126824 reports a single indexed study location in California, North Carolina.

Frequently Asked Questions

What is clinical trial NCT04126824 about?

NCT04126824 is a clinical study titled "Effect of Addition of Steroids on Duration of Analgesia". The purpose of the study is to investigate the differences in post-procedural pain scores and narcotic use among patients who receive a Superior Hypogastric Nerve Block (SHNB) with and without corticosteroid performed as part of the Uterine Artery Embolization (UAE) procedure.

What is the current status of trial NCT04126824?

This trial is currently active not recruiting. It is a Early Phase 1 study. The enrollment target is 28 participants. The study started on 2022-01-06. Estimated completion is 2027-08-02.

What conditions does trial NCT04126824 study?

This clinical trial studies the following conditions: Uterine Fibroids, Adenomyosis.

What interventions are being tested in trial NCT04126824?

The interventions under investigation include: Bupivacaine (DRUG), Triamcinolone (DRUG), Iohexol contrast (OTHER).

Who is sponsoring clinical trial NCT04126824?

This trial is sponsored by University of California, Los Angeles, which has 897 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04126824 being conducted?

This trial has 2 study locations across California, North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Uterine Fibroids

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT04126824's enrollment target sits among peer trials

28 9th of 10 higher than 2 of 10 other Uterine Fibroids trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Uterine Fibroids 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 NCT04126824, the US trial registry maintained by the National Library of Medicine. NCT04126824 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.