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โ† Trials
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Gabapentin Premedication to Reduce Postoperative Pain for Pediatric Tonsillectomy

RecruitingPhase 4Ages 3 Years - 18 YearsAllChildren's Healthcare of Atlanta
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In plain words

What the trial is, and whether it could suit you

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. We hypothesize one 15mg/kg (up to 600mg) dose of gabapentin will decrease mean narcotic amounts in mg/kg compared to participants who do not receive preoperative gabapentin and will demonstrate a decreased mean time to first analgesic as well as to lower mean pain scores for each age group at 12, 24 and 48 hours.

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * participants age 3-18 years * ASA class 1 or 2 * elective Tonsillectomy/Adenoidectomy * outpatient setting. Exclusion Criteria: * BMI \>40kg/m2 * history of renal insufficiency, chronic pain * allergy to gabapentin * history of developmental delay
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What it tests

  • Gabapentin
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Where

1 site
Children's Healthcare of Atlanta
Atlanta, United States
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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