Postoperative pain from anorectal diseases
Conditions
Interventions
Content Group A (Control Group):Homemade external ointment free of borneol and Corydalis.
Group B (Experimental Group 1):Homemade external ointment containing 3 g borneol and 20 g Corydalis.
Group C (experimental group 2):Self-made ointment for external use, composed of 3 g borneol and 40 g Corydalis.
Group D (Experimental Group 3):Self-made ointment for external use, containing 3 g borneol and 60 g Corydalis.
Group E (Experimental Group 4):Self-made ointment for external use, containing 3 g borneol and 80 g Corydalis.
Sponsors
Taixing Hospital of Traditional Chinese Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: According to the 2022 edition of the "Guidelines for the Diagnosis and Treatment of Anorectal Diseases" regarding the diagnosis of piles, fistulas, fissures, and perianal abscesses, and the 2021 edition of "Traditional Chinese Surgery" (edited by Chen Hongfeng and published by China Traditional Chinese Medicine Press) regarding the diagnosis of piles, fistulas, fissures, and perianal abscesses: (1) Patients who meet the diagnostic criteria of both traditional Chinese and Western medicine and are scheduled to undergo surgical treatment in our hospital's anorectal surgery department. (2) Patients aged between 18 and 65 years old, who voluntarily participate in this study and sign the informed consent form. (3) Patients without comorbidities that affect pain assessment, without underlying diseases that impact spinal anesthesia or postoperative recovery, and without a history of allergy to Chinese herbal medicine or topical medications. (4) Patients who are able to report VAS pain scores accurately and on time, and to undergo routine blood tests and hypersensitive C-reactive protein level examinations as scheduled.
Exclusion criteria
Exclusion criteria: (1) Patients found to have contraindications for surgery or unable to meet all the inclusion criteria simultaneously during hospital admission examination. (2) Individuals lacking the ability to make accurate judgments or unable to cooperate properly with data collection for the study. (3) Participants with emotional abnormalities, poor compliance, or refusal to cooperate. (4) Pregnant women, postpartum individuals, or patients unable to tolerate any drug side effects. (5) Participants experiencing unforeseen extraordinary events during the study period that prevent timely completion of the research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Recovery speed;Absolute neutrophil count, percentage of neutrophils, and high-sensitivity C-reactive protein.; | — |
Countries
China
Contacts
Public ContactSunyan
Taixing Hospital of Traditional Chinese Medicine
Outcome results
None listed