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ICE-T Pain Regimen for Total Laparoscopic Hysterectomy

NCT03987022 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2025-01-24

Study results available
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Summary

The purpose of this randomized controlled trial is to determine whether, "ICE-T," a multimodal postoperative pain regimen composed of around the clock ice packs, toradol, and tylenol, has improved pain control compared to the standard narcotic based postoperative pain regimen in patients undergoing total laparoscopic gyn surgery.

Conditions

  • Opioid Substitution Treatment

Interventions

DRUG

Ketorolac

Use of non-steroidal anti-inflammatory drug for pain control postoperatively

DRUG

Opioids

Use of narcotic for pain control postoperatively

OTHER

Ice Packs

Placement of Ice packs on surgical sites postoperatively

DRUG

Tylenol

Use of pain medication postoperatively

DRUG

Motrin

Use of non-steroidal anti-inflammatory drug for pain control postoperatively

DRUG

Dilaudid Injectable Product

Use of narcotic for pain control postoperatively

DRUG

Percocet 5Mg-325Mg Tablet

Use of combination tablet of Tylenol and Oxycodone for pain control postoperatively

Sponsors & Collaborators

  • MetroHealth Medical Center

    lead OTHER

Principal Investigators

  • Robert Pollard, MD · MetroHealth Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-01
Primary Completion
2022-04-25
Completion
2022-04-25
FDA Drug
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03987022 on ClinicalTrials.gov