Acupuncture on Postoperative Pain Relief in Patients Undergoing Laparoscopic Cholecystectomy
Effect of Acupuncture on Postoperative Pain Relief in Patients Undergoing Laparoscopic Cholecystectomy in Suez Canal University Hospitals: A Randomized Controlled Trial
1 other identifier
interventional
50
1 country
1
Brief Summary
To lessen related side effects, opioids are used as needed to treat pain after laparoscopic cholecystectomy (LC). Research into the efficacy of acupuncture as an adjunct treatment for postoperative patients has gained traction. However, the findings of these studies are inconsistent. It has been suggested that acupuncture may not influence postoperative pain, whereas studies involving various surgical procedures have reported favorable results. Nonetheless, there is scant evidence demonstrating the effectiveness of acupuncture in managing pain following LC. In order to assess the effectiveness and safety of acupuncture in reducing postoperative pain in patients following LC, this study was created. The study's objective was to reduce postoperative pain in order to improve the results of LC surgeries. Fifty patients participated in this prospective randomized controlled interventional study, split equally between two groups.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 15, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
March 30, 2025
CompletedFirst Submitted
Initial submission to the registry
July 31, 2025
CompletedFirst Posted
Study publicly available on registry
August 7, 2025
CompletedAugust 7, 2025
July 1, 2025
10 months
July 31, 2025
July 31, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Post-operative pethidine
The total amount of pethidine required to manage pain following surgery
From the moment the surgery was completed until 24 hours after the procedure
Study Arms (2)
Acupuncture
ACTIVE COMPARATORInterventional group: included 25 patients for Acupuncture
Control
NO INTERVENTIONControl patients: included 25 patients who received no intervention.
Interventions
Eligibility Criteria
You may qualify if:
- Patients who are undergoing laparoscopic cholecystectomy of both sexes.
- Patients with grades I and II from the American Society of Anesthesiologists (ASA).
You may not qualify if:
- Patients with local skin infections at acupoints.
- Patients who have nerve injuries on upper limbs or lower limbs.
- Patients who are alcoholics.
- Pregnant.
- Patients with other severe systemic diseases and serious mental illnesses.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Faculty of medicine, Suez Canal University
Ismailia, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- professor of anaesthesia
Study Record Dates
First Submitted
July 31, 2025
First Posted
August 7, 2025
Study Start
January 15, 2024
Primary Completion
November 1, 2024
Study Completion
March 30, 2025
Last Updated
August 7, 2025
Record last verified: 2025-07
Data Sharing
- IPD Sharing
- Will not share