RECRUITING

Ketorolac in Palatoplasty

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

Ketorolac in Palatoplasty: A Randomized Blinded Controlled Trial.

Quick Facts

Study Start:2021-09-17
Study Completion:2026-01-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT04771156

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:6 Months
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. * Syndromic Cleft Palate patients
  2. * Previous palatoplasty
  3. * Major unrepaired cardiac malformation
  4. * History of GI complications (GI Bleed, Gastric Ulceration)
  5. * History of Renal disorder
  6. * History of coagulopathy (As contraindication to NSAID use)
  7. * Feeding tube dependency
  8. * Patients whose parents refuse to consent to randomization

Contacts and Locations

Study Contact

Matthew R Greives, MD,MS,FACS
CONTACT
(713) 500-7275
Matthew.R.Greives@uth.tmc.edu
Alfredo Cepeda Jr., MD
CONTACT
(713) 500-7216
Alfredo.Cepeda@uth.tmc.edu

Principal Investigator

Matthew R Grieves, MD,MS,FACS
PRINCIPAL_INVESTIGATOR
The University of Texas Health Science Center, Houston

Study Locations (Sites)

The University of Texas Health Science Center at Houston
Houston, Texas, 77030
United States

Collaborators and Investigators

Sponsor: The University of Texas Health Science Center, Houston

  • Matthew R Grieves, MD,MS,FACS, PRINCIPAL_INVESTIGATOR, The University of Texas Health Science Center, Houston

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-09-17
Study Completion Date2026-01-31

Study Record Updates

Study Start Date2021-09-17
Study Completion Date2026-01-31

Terms related to this study

Additional Relevant MeSH Terms

  • Cleft Lip and Palate