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Effects of electroacupuncture on postoperative pain and gastrointestinal motility after laparoscopic appendectomy

Effects of electroacupuncture on postoperative pain and gastrointestinal motility after laparoscopic appendectomy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CRIS
Registry ID
KCT0001486
Enrollment
87
Registered
2015-05-14
Start date
2015-05-18
Completion date
Unknown
Last updated
2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Procedure/Surgery : Prospective randomized controlled trial with three-arm, parallel-group. 1. Intervention 1 = electroacupuncture Materials: Stainless-steel needle and PG-306 electroacupuncture devi

Sponsors

Dongguk University Gyeongju Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed as appendicitis 2. Female or male patients over 20 years old 3. Patients undergoing laparoscopic appendectomy

Exclusion criteria

Exclusion criteria: 1. Patients who need simultaneous combined surgery (including ileocecectomy) 2. Patients diagnosed with combined other diseases as well as appendicitis, preoperatively or intrapoperatively (e.g. colonic diverticulitis, inflammator bowel disease, pelvic inflammatory disease, etc.) 3. Patients who need postoperative fasting according to preoperative evaluation or intraoperative findings (e.g. panperitonitis with intraperitoneal abscess) 4. Patients under treatment for acute disease other than appendicitis 5. Patients converted to open surgery 6. Patients with cardiac pacemaker 7. Patients with allergy to or phobia of acupuncture needle or electrostimulation 8. Patients with history of syncope or seizure 9. Pregnant women or lactating women 10. Patients with history of abdominal surgery 11. Patients with American Society of Anesthesiologists'(ASA) physical status classification IV 12. Patients who do not consent to clinical trial 13. Patients incapable of reading, understanding, and signing a written consent form (e.g. mentally retarded, blinded, illiterate, foreigners, etc.) 14. Inmates of a prison or institution/hospital

Design outcomes

Primary

MeasureTime frame
Time of first passing flatus after operation

Secondary

MeasureTime frame
Postoperative pain score;Bowel sound per minute;Postoperative nausea and/or vomiting;Time to tolerable water drinking and solid diet after operation;Postoperative analgesics;Postoperative complications;Readmission rate due to postoperative complications;Time to mobilization(self walking) and self support to preoperative level;Postoperative quality of life questionnaire;Postoperative hospital stay;Total cost during hospital stay after operation;Protocol failure rate

Countries

Korea, Republic of

Contacts

Public ContactGangmi Kim

Dongguk University Gyeongju Hospital

gangmi@naver.com

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Mar 15, 2026