Not Yet RecruitingPhase 3ketamine

Ketamine Irrigation Analgesia in Laparoscopic Cholecystectomy

Sponsored by Assiut University

NCT ID
NCT07370181
Target Enrollment
60 participants
Start Date
2026-01-30
Est. Completion
2026-07-10

About This Study

Patients will be assigned randomly to two groups (30 subjects each) to be anesthetized. The study drug will be delivered in opaque bags labeled "study drug" and 60 patients will be allocated in two groups (of 30 patients each) to receive the irrigation at the end of surgery after dissection; irrigation analgesia by 5 ml bupivacaine 0.50% plus 20 ml normal saline (Group N) or 5 ml bupivacaine 0.50% plus 1 mg/kg ketamine (Group K). The volume of irrigation in group K is completed by normal saline to reach a total of 25 ml.

Conditions Studied

Pain

Interventions

  • Normal saline
  • Ketamine

Eligibility

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

* Patients with age ≥18 years of ASA I-II who will be scheduled for elective laparoscopic cholecystectomy under general anesthesia.

Exclusion Criteria:

* History of congenital heart disease
* Hypertension
* Developmental delay, or
* Allergy to study drugs

Interested in this trial?

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

Omar Makram Soliman, MD
CONTACT
00201065491191omar@aun.edu.eg
View on ClinicalTrials.gov
Data Source
ClinicalTrials.gov

Last updated from source