Clinical Trials Directory

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

TypeNameDescription
DRUGGabapentinGabapentin 600mg tablet
DRUGPlaceboPlacebo 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

Source: ClinicalTrials.gov record NCT04230980. Inclusion in this directory is not an endorsement.