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A randomized controlled clinical study of wrist-ankle acupuncture intervention for postoperative pain of mixed hemorrhoids

To study the clinical effect of wrist and ankle acupuncture on the incidence of postoperative pain and urinary retention of mixed hemorrhoids based on pMDT model and preemptive analgesia concept

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084402
Enrollment
Unknown
Registered
2024-05-16
Start date
2024-06-01
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

mixed hemorrhoid

Interventions

Control group:Basic nursing measures were given after the patient returned to the room
Experiment group 1:In experimental group 1, when postoperative pain occurred and VAS score was =3, a wrist and ankle acupuncture was performed by a TCM therapist for the patient, and the retention tim
Experiment group 2:In experimental group 2, when there was no pain after surgery, the TCM therapist conducted a wrist and ankle acupuncture for the patient in advance, and the retention time was 6h.

Sponsors

Jiangsu Provincial Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for hemorrhoids in the "China Hemorrhoid Diagnosis and Treatment Guidelines (2020)"; 2, Age 18-60 years old, male and female; 3. The surgical method was "ultrasound-guided hemorrhoid ligation" and the type of anesthesia was lumbar anesthesia; 4, The patient or guardian informed consent and voluntary test; 5, Normal cognitive function, can cooperate with the collection of clinical data, exclude patients with mental illness;

Exclusion criteria

Exclusion criteria: 1 Combined with other serious proctoanal diseases, such as inflammatory bowel disease, rectal tumors, etc.; 2 History of anorectal surgery, prostatic hyperplasia, urinary tract infection, etc.; 3 Patients with a history of allergy to the drugs or needles involved in this study; 4 Women in the menstrual period, pregnancy or breastfeeding period; 5 Accompanied by pain in other parts or into the urinary tube;

Design outcomes

Primary

MeasureTime frame
visual analogue scale, VAS;

Secondary

MeasureTime frame
Incidence of urinary retention;residual bladder urine volume;

Countries

China

Contacts

Public ContactZe Lu

Jiangsu Provincial Hospital of Traditional Chinese Medicine

1946319798@qq.com+86 139 5182 0681

Outcome results

None listed

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