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NCT06951802RecruitingPhase 4

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

Endometriosis and Pain Treatment by Intraoperative Administration of Low-dose Ketamine A Single-Centre, Prospective, Randomized, Controlled Trial

Source: ClinicalTrials.gov · Last updated 30 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
118 (estimated)
First submitted
16 Apr 2025
Start date
3 Dec 2024
Primary completion date
30 Jun 2025
Lead sponsor
Insel Gruppe AG, University Hospital Bern
NCT number
NCT06951802

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 118
  • From 3 Dec 2024 to the primary completion date, 30 Jun 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Myocardial infarction during the last 30 days prior to surgery

Other illness

  • Liver disease
  • Known malignant hyperthermia
  • Cardiovascular instability or severe heart failure (New York Heart Association classification (NYHA) \> III)
  • Limited peripheral autonomic activity, hypersensitivity to ketamine or propofol or its components

Age

  • Age \< 18 years

Other

  • ASA physical status ≥4
  • Higher-grade atrioventricular block without pacemaker
  • Severe hypovolemia or bradycardia
  • Uncontrolled hyper- or hypotension
  • Increased intracranial or increased intraocular pressure
  • Pregnancy
  • Rejection or lack of consent of the patient or relatives

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Inselspital Bern
Coordinator of this site? Confirm its status
BernSwitzerlandRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.