Pilonidal sinus
Conditions
Interventions
Control group:After surgery, patients regularly go to the hospital to receive dressing change treatment 1-2 times/day from professional medical staff according to the traditional mode
Experimental group:Patients with pilonidal sinus are mainly assisted by family members to change dressings after surgery, change dressings 1-2 times a day, and return to the hospital for reexamination
Sponsors
Peking University First Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Patients between the ages of 18 and 65 years. 2. Patients diagnosed with pilonidal sinus by intraanal ultrasound/spiral CT/magnetic resonance imaging (MRI) and who have failed to respond to long-term or continuous conservative treatment. 3. Patients who have been successfully treated with pilonidal sinus surgery. 4. Patients voluntarily sign the informed consent form for study enrollment
Exclusion criteria
Exclusion criteria: 1. Those who are allergic to the drugs or dressings of this study. 2. Pregnant or lactating patients. 3. Patients with diabetes mellitus, long-term treatment with glucocorticoids and immunosuppressive drugs, and poor general underlying conditions (American Society of Anesthesiologists grade IV-V), who cannot guarantee the completion of home dressing change throughout the process. 4. Severe anxiety, depression, or other mental disorders.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Wound healing; | — |
Secondary
| Measure | Time frame |
|---|---|
| Wound pain level (Numeric Pain Intensity Assessment Scale score);Specific recurrence of the pilonidal sinus (clinical symptoms on MRI assessment);Perioperative complications (wound dehiscence, bleeding, discharge, seroma, infection, etc.); | — |
Countries
China
Contacts
Public ContactZhang Hui
Peking University First Hospital
Outcome results
None listed