RecruitingNot applicableNCT05641844
A Double Blind, Randomized Controlled Study, Evaluating the Safety and Efficacy of RD2 Ver.02 For the Management of Anal Fistulas
Studying Anal fistula
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- RedDress Ltd.
- Intervention
- RD2 Ver.02(device)
- Enrollment
- 110 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2024 – 2028
Study locations (10)
- Karen Zaghiyan, M.D, Los Angeles, California, United States
- Cleveland Clinic, Weston, Florida, United States
- University of Chicago, Chicago, Illinois, United States
- Franciscan Health, Indianapolis, Indiana, United States
- UMASS, Worcester, Massachusetts, United States
- Mayo Clinic, Rochester, Minnesota, United States
- Lenox Hill Hospital, New York, New York, United States
- Allegheny Health Network, Pittsburgh, Pennsylvania, United States
- Brown surgical associates, Providence, Rhode Island, United States
- Sheba Medical Center, Ramat Gan, Israel
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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