Postoperative pain of mixed hemorrhoids
Conditions
Interventions
Acupuncture group:On the basis of the acupuncture therapy of "Zhibian(BL54)to Shuidao(ST28)" manipulationon, the patients in the control group were treated. (if the patient had postoperative pain and
Control group:The patients were given diclofenac double-release enteric-coated capsules, 75 mg of sodium diclofenac double-release enteric-coated capsules, =150 mg for 24 hours, if the patients had po
Sponsors
the affilinated Acunpuncture and Tuina hospital of Shanxi University of Chinese Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: (1) Patients who met the diagnostic criteria of mixed hemorrhoids and had a VAS score =4; (2) Age 18-65 years old, both male and female; (3) Surgical anesthesia is lumbar-hard combined anesthesia; (4) The surgical procedure is external stripping and internal ligation of mixed hemorrhoids, and the surgical operation and dressing change are performed by the same person; (5) Regular diet, normal sleep, and previous physical fitness; (6) Those who voluntarily participate in the study and sign the informed consent form, with good compliance and willing to cooperate with observation and treatment.
Exclusion criteria
Exclusion criteria: (1) Patients receiving other treatments that affect the observational index of this subject; (2) Suffering from other rectal-anal diseases, such as perianal abscess, anal fistula, anal fissure and so on; (3) Patients with abnormalities seen in blood routine, urine routine, stool routine, coagulation, liver and kidney function, electrocardiogram and so on; (4) Patients with serious heart, liver, lung, kidney and other systemic diseases and mental anomalies; (5) Pregnant or lactating women; (6) Patients with infectious diseases such as hepatitis B and tuberculosis; (7) Local skin presence of skin infection or skin disease, not suitable for acupuncture; (8) Patients with previous allergic reactions to diclofenac sodium double-release enteric capsules; (9) Patients who are also participating in other clinical studies. Note: Patients who met any of the above were excluded.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Use of painkillers;Occurrence of postoperative complications;Side effects of pain medications;Quality of Life Scale (QLQ-C30);Duration of pain; | — |
Countries
China
Contacts
Public ContactHaijun Wang
the affilinated Acunpuncture and Tuina hospital of Shanxi University of Chinese Medicine
Outcome results
None listed