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Optimizing Perioperative Analgesia to Lower Pain Following Cleft Palate Surgery

Name: Optimizing Perioperative Analgesia to Lower Pain Following Cleft Palate Surgery — clinical trial record (NCT06962306)
Creator: DataLookout
License: https://creativecommons.org/licenses/by/4.0/

Study acronym: OPAL-Cleft

StatusRecruiting

PhasePhase 4

SponsorDuke University

Started2025-06-04

View on ClinicalTrials.gov ↗

Amendment history

2026-04-10

Study Status v3

Re-verified, no change to tracked fields

2025-06-11

Study Status v2

Primary completion date2026-05-15→2027-06-04

Completion date2026-06-15→2027-07-04

Start dateestimated 2025-06-15→confirmed 2025-06-04

2025-05-23

Not Yet Recruiting→Recruiting Study Status, Contacts/Locations v1

Trial statusNot Yet Recruiting→Recruiting

Start date2025-05-15→2025-06-15

Study sitesdetails revised at 1 of 1 site

2025-04-30

Original filing

Duke University

455 trials monitored

See 53 trials at risk

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.

Trial Details

NCT Number	NCT06962306
Lead Sponsor	Duke University
Conditions	Cleft Palate, Pain, Postoperative Care, Perioperative Care, Children
Enrollment	60 participants
Start Date	2025-06-04
Primary Completion	2027-06-04 (estimated)
Study Completion	2027-07-04 (estimated)
Updated on ClinicalTrials.gov	2026-04-14