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Clinical study of buccal acupuncture for postoperative analgesia of mixed hemorrhoids

Clinical study of buccal acupuncture for postoperative analgesia of mixed hemorrhoids

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068683
Enrollment
Unknown
Registered
2023-02-27
Start date
2022-01-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Postoperative analgesia

Interventions

Sponsors

Beilun District Traditional Chinese Medicine Hospital, Ningbo City, Zhejiang Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) All patients who meet the diagnostic criteria for III and IV degree mixed hemorrhoids need surgery; (2) The age range is 20-60 years old, male or female patients are not limited, and the course of disease is 1-10 years; (3) The surgeon in charge of the operation is the same senior physician, and the operation methods are external stripping and internal ligation, and the anesthesia methods are ultrasound-guided sacral anesthesia. Patients who voluntarily cooperate with postoperative pain treatment of hemorrhoids are listed as the research objects; (4) No other serious complications; (5) Patients with clear consciousness, informed consent, cooperation with examination and adherence to treatment; (6) those who signed the informed consent form for entering the research;

Exclusion criteria

Exclusion criteria: (1) Patients with severe cognitive impairment, cardiovascular, liver and kidney, hematopoietic system or systemic diseases, such as psychosis, tumor and leukemia; (2) Patients with other perianal diseases such as severe skin lameness, anal fissure, perianal abscess, rectal malignant tumor and intestinal infection; (3) those who use analgesics within 12 hours before operation and other analgesics after operation; (4) Bilateral facial skin is not suitable for buccal acupuncture; (5) Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
visual analogue scale score;Pressing times of analgesic pump;numerical rating scale;

Secondary

MeasureTime frame
VOMIT;headache;

Countries

China

Contacts

Public ContactYang jianbing
88118009@qq.com13586552293

Outcome results

None listed

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