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The Effect of Acupressure on Postoperative Pain After Laparoscopic Totally Extraperitoneal Inguinal Hernia Repair: A Prospective Three-Arm Randomized Sham-Controlled Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This randomized, sham-controlled clinical trial aims to evaluate the effect of acupressure on postoperative pain following laparoscopic totally extraperitoneal (TEP) inguinal hernia repair. A total of 90 participants will be randomly assigned to one of three groups: standard postoperative care alone (control group), true acupressure plus standard care, or sham acupressure plus standard care. Acupressure will be applied at postoperative hours 1, 4, and 8 using the bilateral P6 (Neiguan), LI4 (Hegu), ST36 (Zusanli), and SP6 (Sanyinjiao) acupoints. The sham group will receive pressure at non-acupuncture points. The primary outcome is postoperative pain intensity measured using the Visual Analog Scale (VAS). Secondary outcomes include analgesic consumption, postoperative nausea and vomiting, time to mobilization, patient satisfaction, and postoperative complications.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: f
View:

• Adults aged 18 to 75 years

• Diagnosis of a unilateral primary inguinal hernia

• Scheduled to undergo elective laparoscopic total extraperitoneal (TEP) inguinal hernia repair

• American Society of Anesthesiologists (ASA) physical status I to III without an anticipated need for postoperative intensive care

• Ability to understand the study procedures and provide written informed consent

Locations
Other Locations
Turkey
Fatih Sultan Mehmet Training and Research Hospital
RECRUITING
Istanbul
Contact Information
Primary
AHMET S YAZ, MD
ahmet.yaz@std.medipol.edu.tr
+902165783000
Time Frame
Start Date: 2026-06-20
Estimated Completion Date: 2026-10-31
Participants
Target number of participants: 90
Treatments
No_intervention: Control
Participants receive standard postoperative care without acupressure.
Experimental: Acupressure
Participants receive standard postoperative care plus true acupressure at bilateral P6, LI4, ST36, and SP6 points for 3 minutes per point at postoperative 1, 4, and 8 hours.
Sham_comparator: Sham Acupressure
Participants receive standard postoperative care plus sham acupressure at non-acupoint locations with the same duration and schedule as the acupressure group.
Related Therapeutic Areas
Sponsors
Leads: Medipol University
Collaborators: Fatih Sultan Mehmet Training and Research Hospital

This content was sourced from clinicaltrials.gov