Actively Recruiting
Endometriosis and Pain Treatment by Intraoperative Administration of Low-dose Ketamine
Led by Insel Gruppe AG, University Hospital Bern · Updated on 2025-04-30
118
Participants Needed
1
Research Sites
108 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
RCT comparing intraoperative administration of low-dose ketamine during laparoscopic endometriosis operation and the postoperative pain outcome
CONDITIONS
Official Title
Endometriosis and Pain Treatment by Intraoperative Administration of Low-dose Ketamine
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing surgery for endometriosis operation requiring general anaesthesia at the Inselspital, Bern University Hospital, University of Bern, Department of gynaecology and obstetrics.
- Age ≥ 18 years
- American Society of Anesthesiologist (ASA) physical status 1-3
- Patients with known or suspected endometriosis
- Written informed consent.
You will not qualify if you...
- Age < 18 years
- ASA physical status ≥4
- Higher-grade atrioventricular block without pacemaker
- Severe hypovolemia or bradycardia
- Uncontrolled hyper- or hypotension
- Liver disease
- Known malignant hyperthermia
- Cardiovascular instability or severe heart failure (New York Heart Association classification (NYHA) > III)
- Myocardial infarction during the last 30 days prior to surgery
- Increased intracranial or increased intraocular pressure
- Limited peripheral autonomic activity, hypersensitivity to ketamine or propofol or its components
- Pregnancy
- Rejection or lack of consent of the patient or relatives
AI-Screening
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Trial Site Locations
Total: 1 location
1
Inselspital Bern
Bern, Switzerland, 3010
Actively Recruiting
Research Team
C
Christian Vetter, MD
CONTACT
G
Gianluca Comazzi, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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