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To study the effect and mechanism of wrist and ankle acupuncture preemptive analgesia on pain after hemorrhoidectomy based on skin theory

To study the effect and mechanism of wrist and ankle acupuncture preemptive analgesia on pain after hemorrhoidectomy based on skin theory

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000923
Enrollment
Unknown
Registered
2025-05-07
Start date
2025-05-31
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

mixed hemorrhoid

Interventions

Test group 1:Wrist and ankle acupuncture advanced analgesia combined with basic analgesia measures
blank group:Basic analgesia measures were given
Test group 2:Wrist and ankle needle pseudoacupuncture advance analgesia combined with basic analgesia measures

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) Patients with grade ?-? mixed hemorrhoids who meet the diagnostic criteria for hemorrhoids in the "Chinese Hemorrhoids Diagnosis and Treatment Guidelines (2020)" and have surgical indications; (2) Age 18-60 years old male or female; (3) The surgical method was "ultrasound-guided hemorrhoidectomy" and the type of anesthesia was lumbar anesthesia; (4) The function of vital organs in the whole body is basically normal no major diseases; (5) Normal cognitive function able to cooperate with the collection of clinical data; (6) The patient or the patient's guardian gives informed consent and voluntarily takes the test;

Exclusion criteria

Exclusion criteria: (1) Combined with other serious proctoanal diseases such as inflammatory bowel disease rectal tumors etc.; (2) Previous history of prostatic hyperplasia urinary tract infection thrombosis digestive disease etc.; (3) Patients who are allergic to drugs or needles involved in this clinical trial study; (4) Women in the menstrual period pregnancy or breastfeeding period and women with a history of abortion; (5) accompanied by pain in other parts or into the urinary tube;

Design outcomes

Primary

MeasureTime frame
HR \SPO2 \MAP;VAS;

Secondary

MeasureTime frame
Incidence of adverse drug reactions;IL-6\TNF-a\PG;PASS-20;Incidence of urinary retention;Additional dose of analgesic;

Countries

China

Contacts

Public ContactHe Pingping

Traditional Chinese Medicine of Jiangsu Provincial Hospital

1204741797@qq.com15251865684

Outcome results

None listed

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