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Clinical study on incision and drainage of perianal abscess under combined acupuncture anesthesia

Clinical study on incision and drainage of perianal abscess under combined acupuncture anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2200006720
Enrollment
Unknown
Registered
2022-10-29
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

perianal abscess

Interventions

Experimental group:Acupuncture anesthesia was administered 40 minutes before the operation
Control group:None

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who corresponding to diagnostic criteria for perianal abscess. Having the following low abscesses diagnosing by physical examination or auxiliary examination: perianal subcutaneous abscess, ischiorectal abscess, posterior anal space abscess or low intermuscular abscess. 2.Patients who meet the diagnostic criteria of traditional Chinese medicine for Gang Yong and are dialectically certified as hot and toxic burning syndrome or heat and toxic accumulation. 3.To perform perianal abscess incision under local anesthesia. 4. Age =18 years old and =70 years old, both sexes. 5 Understand and agree to participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with severe hematopoietic system diseases or immune system diseases. 2. Long-term history of alcoholism, mental illness and consciousness disorders. 3. Patients treated with opioids within three months. 4. There are contraindications of acupuncture anesthesia: such as metal allergy, needle sickness, or local skin infection and ulceration are not suitable for acupuncture. 5. Participants who participated in or are participating in other clinical trials within one month before enrollment.

Design outcomes

Primary

MeasureTime frame
VAS score;

Secondary

MeasureTime frame
Times and doses of analgesics after operation;The anesthesia time;Wound healing status;Intraoperative lidocaine dosage;The incidence of postoperative complications;Amsterdam Preoperative Anxiety and Information Scale;Satisfaction with surgical anesthesia;The operation time;C-reactive protein;Intraoperative vital signs;State-trait anxiety inventory;

Countries

China

Contacts

Public ContactWang Zhenyi
drxinhuo@163.com13601760317

Outcome results

None listed

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