Gabapentin Premedication to Reduce Postoperative Pain for Pediatric Tonsillectomy
NCT03625011
This study is recruiting at 1 US site in 1 state, according to its ClinicalTrials.gov record last updated .
Summary
The purpose of this pilot study: 1) to examine the use of gabapentin in reducing pain in the first 48 hours postoperatively including the total amount of narcotics mg/kg given 2) to record the time to first analgesic postoperatively and 3) to compare Wong Baker and the 0-10 numeric pain distress scale scores at 12, 24 and 48 hours postoperatively.
Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov
Conditions studied
- Tonsillitis
- Tonsillectomy
Eligibility basics and study details
- Study type
- Interventional
- Phase
- Phase 4
- Ages
- 3 to 18 years
- Sex
- All
- Healthy volunteers
- Accepted
- Sponsor
- Children's Healthcare of Atlanta
- Last updated on ClinicalTrials.gov
- July 24, 2019
These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.
US recruiting sites
Georgia · 1
- Children's Healthcare of Atlanta · Atlanta, GA
Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.