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Intraoperative Methadone for Postoperative Pain in Patients Undergoing Tonsillectomy

NCT05445856 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 130

Last updated 2023-12-05

No results posted yet for this study

Summary

A randomized controlled trial evaluating the efficacy and safety of single-shot intraoperative methadone for postoperative pain in patients undergoing tonsillectomy. Fentanyl is used as an active comparator

Conditions

  • Postoperative Pain

Interventions

DRUG

Methadone

Methadone is administered as a single intravenous dose after induction of anesthesia and prior to initiation of surgery

DRUG

Fentanyl

Fentanyl is administered as a single intravenous dose after induction of anesthesia and prior to initiation of surgery

Sponsors & Collaborators

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Lone Nikolajsen, PhD, DMSc · Aarhus University Hospital, Department of Anesthesia and Intensive Care

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-11-28
Primary Completion
2024-01-31
Completion
2024-08-31

Countries

  • Denmark

Study Locations

More Related Trials

Entities

Drugs

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 NCT05445856 on ClinicalTrials.gov