Efficacy and Safety Study of a Medical Device (KULIST)to Treat Perianal Fistulas
NCT01462747 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 28
Last updated 2013-02-13
Summary
The aim of this study is to evaluate the effects of rectally administered activated carbon (medical device KULIST) in chronic, uncomplicated, perianal fistulas.
Conditions
- Perianal Fistulas
Interventions
- DEVICE
-
KULIST
Twice daily dosing for 8 weeks
Sponsors & Collaborators
-
Nordic Drugs AB
lead INDUSTRY
Principal Investigators
-
Måns Bohe, MD, PhD · Skane University Hospital
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2011-12-31
- Primary Completion
- 2012-06-30
- Completion
- 2013-01-31
Countries
- Sweden
Study Locations
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