Condition: Dental Pain and Sensation Disorder · Pain, Postoperative · Sponsor: Loma Linda University
This study is a double-blind, randomized, prospective, placebo-controlled single-center clinical research study in which 600 mg of gabapentin or placebo will be administered 2 hours preoperatively to 49 patients each undergoing wisdom teeth extraction. We will measure intraoperative opioid use, severity of pain, the number of analgesics taken, and side effect profiles (e.g. nausea/vomiting, dizziness) at the following intervals, 4 hour, 8 hour, 12 hour, 24, and 72 hour post-procedure.
This description comes directly from the study's public registry record.
Je Dong Ryu, DMD MD · 909-558-4423 · jryu@llu.edu
Sung Han, DDS MD · 909-558-4423 · shan@llu.edu
Always discuss trial participation with your own doctor first.
| Loma Linda University Health | Loma Linda, California, United States | Recruiting |
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT04860141