Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT06962306
PHASE4

Optimizing Perioperative Analgesia to Lower Pain Following Cleft Palate Surgery

Sponsor: Duke University

View on ClinicalTrials.gov

Summary

The purpose of this study is to compare the use of short acting opioids (fentanyl/hydromorphone) with long acting opioids (methadone) for pain control following cleft palate surgery in infants and young children.

Official title: Perioperative Methadone Use for Cleft Palate Repair: A Randomized Controlled Trial

Key Details

Gender

All

Age Range

6 Months - 4 Years

Study Type

INTERVENTIONAL

Enrollment

60

Start Date

2025-06-04

Completion Date

2027-07-04

Last Updated

2025-06-13

Healthy Volunteers

No

Interventions

DRUG

Methadone hydrochloride

Initial dosing 0.2mg/kg, potential to escalate to 0.25mg/kg following interim analysis

DRUG

Fentanyl/Hydromorphone

Per routine care

Locations (1)

Duke University Medical Center

Durham, North Carolina, United States