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ED90 of 0.75% Bupivacaine for Bilateral Tubal Ligation (BTL)

Pain Clinical Trial

Official title:
Determining the ED90 for Intrathecal 0.75% Hyperbaric Bupivacaine for Bilateral Tubal Ligation

Clinical Trial Summary

The purpose of this study is to determine the dose of bupivacaine that provides effective pain management in 90% (ED90) of patients undergoing bilateral tubal ligation. This will guide anesthesiologists on the most effective dose to minimize intraoperative pain during this procedure. The goal is to make women as comfortable as possible when they undergo this procedure while also minimizing the amount of time they are required to remain in the hospital afterwards for monitoring.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05017584
Study type Interventional
Source Duke University
Contact
Status Withdrawn
Phase Phase 4
Start date January 2023
Completion date January 1, 2024
View Details
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