High Perianal Abscess
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Patients diagnosed with high grade perianal abscess (the diagnosis is heat-toxin-containing knot syndrome) and undergoing surgery for virtual and real hanging wire (multi-incision floating wire drainage); 2) Age between 18 and 60 years old; 3) Blood urine feces routine bleeding and coagulation time liver and kidney function blood glucose electrocardiogram are within the normal range; 4) Normal cognitive function with basic communication and exchange ability; 5) Good compliance to the researcher's observation and treatment Voluntary Participate in the clinical observation trial and sign the consent form; 6) Voluntarily participate in this project and sign the informed consent form.
Exclusion criteria
Exclusion criteria: The existence of any one of the following conditions are excluded: 1) tuberculosis leukemia trauma immune diseases Crohn's disease and inflammatory bowel disease and other specific perianal abscess; 2) combined with systemic diseases such as malignant neoplasms diabetes mellitus severe hypertension hematological system and other primary diseases; 3) combined with gastrointestinal disorders such as chronic constipation chronic diarrhea etc.; 4) serious heart brain liver lungs kidneys and other important organ diseases and mental illnesses; 5) combined with other anal diseases such as rectal prolapse anal eczema rectal polyps etc.; 6) previous patients with heart brain liver lung kidney and other major organ diseases and mental illnesses; 5) combined with other anal diseases such as prolapsed rectum Patients with severe heart brain liver lung kidney and other important organ diseases and mental diseases; 5) patients with other anal diseases such as rectal prolapse anal eczema rectal polyps etc.; 6) patients with a history of anal surgery or abnormal anal morphology and function; 7) patients with infectious diseases such as tuberculosis hepatitis B sexually transmitted diseases etc.; 8) women in pregnancy or breastfeeding; 9) patients who participate in other clinical experimental research.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| IL-6(Interleukin 6);IL-1ß(Interleukin 1 beta);TNF-a(Tumor Necrosis Factor-alpha); | — |
Secondary
| Measure | Time frame |
|---|---|
| Wound secretion;Wound healing;pain in the wound; | — |
Countries
China
Contacts
Hospital of Chengdu University of Traditional Chinese Medicine