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Tissue Grafting
liquid buccal mucosa graft for Urethral Stricture (LBMG Trial)
Phase 1
Waitlist Available
Led By Dmitriy Nikolavsky, MD
Research Sponsored by State University of New York - Upstate Medical University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 years
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new, minimally-invasive treatment for urethral strictures (narrowing of the urethra). The current standard of care is either endoscopic urethrotomy (DVIU) or open reconstruction (urethroplasty), both of which have drawbacks. This trial is testing whether a new technique using a combination of existing surgical techniques, augmented by a buccal mucosal graft, is feasible and effective.
Eligible Conditions
- Urethral Stricture
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Voiding Surgical Outcomes: Stricture Recurrence
Secondary study objectives
Immediate Perioperative Outcomes
Patient Satisfaction
Short-term Postoperative Outcomes
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: liquid buccal mucosa graftExperimental Treatment1 Intervention
DVIU treated with liquid buccal mucosal graft; endoscopic injection of morcellated buccal mucosal graft mixed with fibrin glue
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Who is running the clinical trial?
State University of New York - Upstate Medical UniversityLead Sponsor
174 Previous Clinical Trials
27,491 Total Patients Enrolled
Dmitriy Nikolavsky, MDPrincipal InvestigatorState University of New York - Upstate Medical University
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