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NCT06925152 · ClinicalTrials.gov registry record · Phase 4

COMFORT Trial: Complex Obstetric Management With Focused Regional Transversus Abdominis Plane Block

A Phase 4 study of Cesarean Delivery and Complex Obstetric Surgery, sponsored by University of Tennessee.

Recruiting
Registry status
Phase 4
Development phase
120
Enrollment target
1
Study location

NCT06925152 is a Phase 4 study of Cesarean Delivery and Complex Obstetric Surgery that is actively recruiting participants, run by University of Tennessee. The registered enrollment target is 120 participants, below the 3,471-participant average among 10 other Cesarean Delivery trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06925152, a Phase 4 study of Cesarean Delivery and Complex Obstetric Surgery, is actively recruiting participants, sponsored by University of Tennessee.

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

Study Summary

To assess the effect of intraoperative transversus abdominis plane (TAP) blocks on the amount of opioid pain medications expressed as morphine milliequivalents (MME) used postoperatively in patients who have undergone cesarean delivery (CD) in the setting of complex obstetric surgery (COS).

Conditions Studied

Cesarean Delivery Complex Obstetric Surgery Perioperative Pain Management Postoperative Pain Control

Interventions

  • DRUG Bupivicaine intervention arm
  • DRUG Placebo arm

Study Locations (1)

Tennessee

  • Regional One Health - Memphis

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2025-07-15
Est. Completion 2028-05
Phase Phase 4

Sponsor

University of Tennessee

96 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06925152

The ClinicalTrials.gov registry entry for NCT06925152 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 3,471-participant average among 10 other Cesarean Delivery trials with a reported enrollment target (97% lower). The listed sponsor is University of Tennessee, which has 96 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with Cesarean Delivery appearing as the primary indexed condition, and to 2 interventions - of which Bupivicaine intervention arm is the first listed.

NCT06925152 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.

Frequently Asked Questions

What is clinical trial NCT06925152 about?

NCT06925152 is a clinical study titled "COMFORT Trial: Complex Obstetric Management With Focused Regional Transversus Abdominis Plane Block". To assess the effect of intraoperative transversus abdominis plane (TAP) blocks on the amount of opioid pain medications expressed as morphine milliequivalents (MME) used postoperatively in patients who have undergone cesarean delivery (CD) in the setting of complex obstetric surgery (COS).

What is the current status of trial NCT06925152?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 120 participants. The study started on 2025-07-15. Estimated completion is 2028-05.

What conditions does trial NCT06925152 study?

This clinical trial studies the following conditions: Cesarean Delivery, Complex Obstetric Surgery, Perioperative Pain Management, Postoperative Pain Control.

What interventions are being tested in trial NCT06925152?

The interventions under investigation include: Bupivicaine intervention arm (DRUG), Placebo arm (DRUG).

Who is sponsoring clinical trial NCT06925152?

This trial is sponsored by University of Tennessee, which has 96 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06925152 being conducted?

This trial has 1 study location across Tennessee. 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.