RecruitingPhase 4

Ketorolac in Palatoplasty

United States74 participantsStarted 2021-09-17

Plain-language summary

The purpose of this study is to see if the addition of IV Ketorolac to usual care multi-modal pain therapy compared to usual care will improve oral intake post-operatively

Who can participate

Age range6 Months

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓Patient with Cleft palate (Complete and incomplete), with or without cleft lip, unilateral or bilateral

What they're measuring

Volume of oral intake

Timeframe: from arrival to Post-Anesthesia Care Unit (PACU) to 24 hours post surgery

Trial details

NCT IDNCT04771156

SponsorThe University of Texas Health Science Center, Houston

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-03-01

Contact for this trial

Matthew R Greives, MD,MS,FACS

(713) 500-7275 Matthew.R.Greives@uth.tmc.edu

View on ClinicalTrials.gov More Cleft Lip and Palate trials