Trials / Completed
CompletedNCT04230980
Gabapentin for Post-Operative Pain Control and Narcotic Reduction in Scrotal Surgery
The Use of Gabapentin for Post-Operative Pain Control and Narcotic Reduction in Scrotal Surgery
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 74 (actual)
- Sponsor
- Weill Medical College of Cornell University · Academic / Other
- Sex
- Male
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The use of non-narcotic multi-modal analgesia to be used in the pre-operative, peri-operative and post-operative period to reduce or potentially eliminate narcotic usage following scrotal surgery. Research study results have shown that the use of anti-inflammatories in the peri-operative period reduces both pain and narcotic use. The hypothesis is that adding another agent in the multi-modal pathway will further reduce pain and potentially reduce narcotic usage.
Detailed description
This is a double-blinded, placebo-controlled, randomized trial that will recruit patients categorized into two study arms. Patients in the gabapentin arm will receive gabapentin 600mg taken pre-operatively and 300mg taken three times a day for 3 days, while patients in the placebo arm will receive a placebo drug taken pre-operatively three times a day for 3 days.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Gabapentin | Gabapentin 600mg tablet |
| DRUG | Placebo | Placebo tablet |
Timeline
- Start date
- 2020-07-28
- Primary completion
- 2022-11-28
- Completion
- 2022-12-16
- First posted
- 2020-01-18
- Last updated
- 2023-10-18
- Results posted
- 2023-10-18
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT04230980. Inclusion in this directory is not an endorsement.