MedTrace Logo

Endometriosis and Pain Treatment by Intraoperative Administration of Low-dose Ketamine

NCT06951802 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 118

Last updated 2025-04-30

No results posted yet for this study

Summary

RCT comparing intraoperative administration of low-dose ketamine during laparoscopic endometriosis operation and the postoperative pain outcome

Conditions

  • Endometriosis

Interventions

DRUG

Ketamine

Low-dose administration of ketamine during laparoscopic surgery

DRUG

Propofol

Control group

Sponsors & Collaborators

  • Insel Gruppe AG, University Hospital Bern

    lead OTHER

Principal Investigators

  • Christian Vetter, MD · Dep. of Anaesthesiology and Pain Medicine, Inselsptial Bern

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-12-03
Primary Completion
2025-06-30
Completion
2026-12-31

Countries

  • Switzerland

Study Locations

More Related Trials

Entities

Drugs

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06951802 on ClinicalTrials.gov