Clascoterone in Pilonidal Sinus (CLIPS Trial)
Brief description of study
- Determine the effect of clascoterone on clinical severity of PSD.
- Analyze the influence of clascoterone in disease-specific quality of life.
- Quantify the effect of clascoterone on surgical outcomes and cutaneous inflammation. 1. Medical photography with independent physician scores of PSD clinical severity at weeks 4, 8, and 12 on treatment 1. Patient reported quality of life scores with the Dermatology Life Quality Index at weeks 4, 8, and 12</li>
- Quantification of markers of inflammation in surgical specimens from PSD resection from those patients who come to surgery
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Medical Research
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Age: 18 years - 99 years
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Gender: All
Participants are eligible for the trial if they are: over 18 years of age, have a diagnosis of pilonidal disease, are willing to apply the cream and come to study visits, and are NOT pregnant, breastfeeding, allergic to clascoterone, have had a fever in 7 days, or are being treated with another investigational drug.
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