Skip to content
Study details
Enrolling now

Superior Hypogastric Nerve Plexus Block With Bupivacaine After Robotic Resection of Endometriosis

Baylor College of Medicine
NCT IDNCT06577233ClinicalTrials.gov data as of Apr 2026
Phase

Phase 4

Target enrollment

60

Study length

about 1 year

Ages

18–65

Sex

Female only

Locations

1 site in TX

What this study is about

This trial is testing if a superior hypogastric nerve plexus block with bupivacaine can reduce postoperative pain and opioid use in women undergoing robotic assisted endometriosis surgery. Researchers will inject either bupivacaine or normal saline into the nerves around the pelvis before surgery, then measure pain levels and opioid usage for 7 days after the procedure.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Bupivacaine Hydrochloride
  • 2.Take Normal saline

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

Anesthetics (Prostaglandin Receptor Antagonists)

Drug routes

injection (Injection)

Endpoints

Primary: Postoperative pain

Secondary: Opioid use

Body systems

Reproductive Health