Acupuncture on Postoperative Pain Relief in Patients Undergoing Laparoscopic Cholecystectomy (NCT07110545) | Clinical Trial Compass
CompletedNot Applicable
Acupuncture on Postoperative Pain Relief in Patients Undergoing Laparoscopic Cholecystectomy
Egypt50 participantsStarted 2024-01-15
Plain-language 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.
Who can participate
Age range
18 Years – 70 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Patients who are undergoing laparoscopic cholecystectomy of both sexes.
* Patients with grades I and II from the American Society of Anesthesiologists (ASA).
Exclusion Criteria:
* 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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Post-operative pethidine
Timeframe: From the moment the surgery was completed until 24 hours after the procedure