mixed hemorrhoids
Conditions
Interventions
Study Group:On the basis of providing routine care to the participants of the mixed hemorrhoids study, TEAS was immediately administered after the completion of the surgical handover. The selected acu
Control group:After the completion of surgical handover, the participants in the mixed hemorrhoid study were immediately given routine care. The participants after surgery used the visual analogue sca
Sponsors
West China Hospital, Sichuan University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: (1) Patients with stage III - IV mixed hemorrhoids who are scheduled for elective surgical treatment; (2) Aged between 18 and 65 years old; (3) Having civil capacity; (4) Having normal structure and function of the lower digestive tract such as the anus and rectum; (5) Being able to cooperate with the inquiry of medical history, physical and specialized examinations, and understand and fill out the survey forms; (6) Signing the surgical and informed consent forms, having good compliance, and being willing to accept the treatment plan.
Exclusion criteria
Exclusion criteria: (1) Participants with severe disorders in the circulatory, nervous, urinary or hematopoietic systems, or with mental illnesses; (2) Participants with digestive tract diseases such as gastric ulcers who cannot take non - steroidal anti - inflammatory drugs; (3) Participants with a history of lower digestive tract surgery; (4) Research participants with other anorectal diseases, such as perianal abscess and rectal polyps; (5) Participants who cannot cooperate with medical staff, are unconscious or incoherent; (6) Participants who are currently participating in other drug clinical trials; (7) Participants with limb movement disorders.
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Postoperative perianal edema score;Postoperative bleeding score;Wound healing time;Patient hospitalization expenses;The length of the patient's hospital stay;Patient treatment satisfaction;The occurrence of adverse reactions during the patient's treatment; | — |
Primary
| Measure | Time frame |
|---|---|
| Postoperative anal pain score; | — |
Countries
China
Contacts
Public ContactXiang Jueying
West China Hospital of Sichuan University
Outcome results
None listed