drugset / Trial / NCT05229653

The Using Postoperative Ketamine and Exploring the Effect on Endometriosis Pain (UPKEEEP) Study

NCT05229653

Phase 1 Terminated 1 enrolled NYU Langone Health
RandomizedParallel-groupSingle-blindTreatment

Summary

This is a randomized, single blinded, placebo-controlled trial to study the effectiveness of a subanesthetic dose (0.6 mg/kg) of ketamine versus placebo (saline) on postoperative pain and pain on adult female chronic pelvic pain patients undergoing robotic removal of endometriosis. The objective of the study is to explore the effect of a sub anesthetic dose of ketamine (0.6 mg/kg) vs. saline control on postoperative pain and recovery in chronic pelvic pain patients who have undergone robotic removal of endometriosis.

Timeline

Start
2022-04-12
Primary completion
2022-10-21
Completion
2022-10-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Ketamine Small molecule 0.6 mg/kg Intravenous

Indications