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Study on reducing postoperative pain of mixed hemorrhoids with auricular acupuncture combined with wrist and ankle acupuncture

Study on reducing postoperative pain of mixed hemorrhoids with auricular acupuncture combined with wrist and ankle acupuncture

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084239
Enrollment
Unknown
Registered
2024-05-13
Start date
2024-05-15
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

Patients undergoing elective mixed hemorrhoid surgery

Interventions

Acupuncture group:Wrist and ankle acupuncture combined with auricular acupuncture remained for 24h. Ask the patient to press the auricular acupuncture independently as required. After treatment, the p
Pseudoacupuncture group:Prosthetic wrist and ankle acupuncture combined with prosthetic auricular acupuncture remained for 24h. Intravenous dezocine is also given when the pain is unbearable.

Sponsors

Jiangsu Province Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age 18-80 years old, gender unlimited; (2) Patients with ASA I-III; (3) Patients undergoing mixed hemorrhoid surgery under elective lumbar anesthesia; (4) Ankle and auricle skin intact, no redness, no scar, no damage; (5) Subjects voluntarily join the study and sign a written informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with other operations in the anorectal department, including patients with anal fissures, anal fistulas, rectal polyps, perianal abscesses, colon polyps, and large intestine lesions; (2) Patients with severe primary hematopoietic system, cardiovascular, liver and kidney diseases; (3) Patients with inflammation, damage, redness and swelling of the skin at the acupuncture site; (4) Fainting needles or unable to cooperate with acupuncture, ear point treatment (5) Cognitive dysfunction, unable to determine the degree of pain; (6) Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
The incidence of pain with a moderate to severe visual analogue score (VAS=4) at rest 24 hours after surgery;

Secondary

MeasureTime frame
Incidence of moderate to severe (VAS=4) pain at rest 48 and 72 hours after surgery;The pain of dressing change and defecation were evaluated by VAS score at 24h, 48h and 72h after operation;Total dosage of postoperative analgesics 24h, 48h and 72h after surgery;Incidence of urinary retention at 24h, 48h and 72h after surgery;Quality of recovery (QOR-15) scores at 24h, 48h and 72h after surgery;

Countries

China

Contacts

Public ContactLi Xuefei

Jiangsu Province Hospital of Chinese Medicine

xuefei9704@126.com+86 134 0416 7289

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026