RecruitingPhase 4ketamine

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

Sponsored by Insel Gruppe AG, University Hospital Bern

NCT ID
NCT06951802
Target Enrollment
118 participants
Start Date
2024-12-03
Est. Completion
2026-12-31

About This Study

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

Conditions Studied

Endometriosis

Interventions

  • Ketamine
  • Propofol

Eligibility

Sex:FEMALE
Age:18 Years - N/A
Healthy Volunteers:No
View full eligibility criteria
Inclusion Criteria:

* 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.

Exclusion Criteria:

* 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

Study Locations (1)

Inselspital Bern
Bern, Switzerland

Interested in this trial?

Contact the study team to learn more about eligibility and enrollment.

Christian Vetter, MD
CONTACT
+416343776christian.vetter@insel.ch
Gianluca Comazzi, MD
CONTACT
+416322111gianluca.comazzi@insel.ch
View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source

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