NCT07110545

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 15, 2024

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2024

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

March 30, 2025

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

July 31, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 7, 2025

Completed
Last Updated

August 7, 2025

Status Verified

July 1, 2025

Enrollment Period

10 months

First QC Date

July 31, 2025

Last Update Submit

July 31, 2025

Conditions

Keywords

acupuncturepostoperative pain

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 COMPARATOR

Interventional group: included 25 patients for Acupuncture

Other: Acupuncture

Control

NO INTERVENTION

Control patients: included 25 patients who received no intervention.

Interventions

Application of acupuncture on specific acupoints

Acupuncture

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

Pain, Postoperative

Interventions

Acupuncture Therapy

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Intervention Hierarchy (Ancestors)

Complementary TherapiesTherapeutics

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

Locations