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NCT06379425 · ClinicalTrials.gov registry record · Phase 4

Impact of Preoperative Opioid-free Multimodal Analgesia on Time to Trial of Void in Ambulatory Urogynecologic Surgeries

A Phase 4 study of Pain, Postoperative and Postoperative Pain, Acute, sponsored by Northwell Health.

Recruiting
Registry status
Phase 4
Development phase
70
Enrollment target
1
Study location

NCT06379425 is a Phase 4 study of Pain, Postoperative and Postoperative Pain, Acute that is actively recruiting participants, run by Northwell Health. The registered enrollment target is 70 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (74% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06379425, a Phase 4 study of Pain, Postoperative and Postoperative Pain, Acute, is actively recruiting participants, sponsored by Northwell Health.

RECRUITING
Registry status
Phase 4
Development phase
70 participants
Enrollment target
1
Study location

Study Summary

This is a double-arm randomized control trial evaluating the impact of preoperative opioid-free analgesia on time to trial of void in ambulatory urogynecologic surgeries. The investigators hypothesize that receipt of acetaminophen, celecoxib and gabapentin preoperatively versus acetaminophen alone will reduce the time to trial of void in patients undergoing same-day minor urogynecologic procedures.

Conditions Studied

Pain, Postoperative Postoperative Pain, Acute

Interventions

  • DRUG Acetaminophen
  • DRUG Celecoxib
  • DRUG Gabapentin

Study Locations (1)

New York

  • Northwell Health South Shore Surgery Center - Bay Shore

Trial Details

FieldValue
Enrollment Target 70 participants
Start Date 2024-03-01
Est. Completion 2026-03-01
Phase Phase 4

Sponsor

Northwell Health

370 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06379425

The ClinicalTrials.gov registry entry for NCT06379425 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 70 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (74% lower). The listed sponsor is Northwell Health, which has 370 total studies on file at ClinicalTrials.gov.

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

NCT06379425 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.

Frequently Asked Questions

What is clinical trial NCT06379425 about?

NCT06379425 is a clinical study titled "Impact of Preoperative Opioid-free Multimodal Analgesia on Time to Trial of Void in Ambulatory Urogynecologic Surgeries". This is a double-arm randomized control trial evaluating the impact of preoperative opioid-free analgesia on time to trial of void in ambulatory urogynecologic surgeries. The investigators hypothesize that receipt of acetaminophen, celecoxib and gabapentin preoperatively versus acetaminophen alone w...

What is the current status of trial NCT06379425?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 70 participants. The study started on 2024-03-01. Estimated completion is 2026-03-01.

What conditions does trial NCT06379425 study?

This clinical trial studies the following conditions: Pain, Postoperative, Postoperative Pain, Acute.

What interventions are being tested in trial NCT06379425?

The interventions under investigation include: Acetaminophen (DRUG), Celecoxib (DRUG), Gabapentin (DRUG).

Who is sponsoring clinical trial NCT06379425?

This trial is sponsored by Northwell Health, which has 370 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06379425 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.