A Study Of Cryptoglandular Fistula-in-ano And Associated Non-healing Draining Wounds With Kerecis SurgiClose - Join Clinical Trial NCTNCT07098715
How to Join This Clinical Trial - NCTNCT07098715
Learn how to participate in this NA trial studying an investigational therapy for Fistula-in-ano, Draining Wound. Current status: NOT_YET_RECRUITING.
Am I Eligible for This Clinical Trial?
This clinical research study is looking for participants with Fistula-in-ano, Draining Wound. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.
- Condition Being Studied
- Fistula-in-ano, Draining Wound
- Treatment Being Tested
- Investigational treatment
- Study Phase
- NA - Research study
- Enrollment Status
- NOT_YET_RECRUITING
- Study Identifier
- NCTNCT07098715 - ClinicalTrials.gov Identifier
- Sponsored By
- Study sponsor
What to Expect as a Participant
Participating in this clinical trial involves:
- Initial screening to determine eligibility
- Regular study visits and health assessments
- Receiving the study treatment or placebo
- Medical monitoring and follow-up care
- Contributing to medical research that may help others
- Potential access to new treatments before they're widely available
Clinical Trial Benefits and Compensation
Participants in this clinical research study may receive:
- Close medical monitoring by healthcare professionals
- Access to potential new treatments
- Compensation for time and travel (varies by study)
- No-cost study-related medical care
- The opportunity to help advance medical knowledge
Where Is This Clinical Trial Located?
This study is enrolling participants at 1 locations. Find a study site near you:
Clinical Research Site
Rochester, Minnesota 55905 - United States
Status: Contact for availability
How to Enroll in This Study
To learn more about participating in this NA clinical trial for Fistula-in-ano, Draining Wound:
- Review the eligibility criteria with your healthcare provider
- Contact the study team for a pre-screening interview
- Schedule an in-person screening visit if eligible
- Review and sign the informed consent form
- Begin participation in the clinical trial
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