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Early Phase 1 N=53 Treatment

ROBUST I Pilot Study, Re-Establishing Flow Via Drug Coated Balloon For The Treatment Of Urethral Stricture Disease

Stricture Urethra

Enrolled (actual)
53
Serious AEs
9.4%
Results posted
Mar 2024
Primary outcome: Primary: Rate of Treatment Related Serious Complication — 0 percentage of participants

Study Design & Population

Study type
Interventional
Phase
Early Phase 1
Interventions
Urotronic Drug Coated Balloon (DCB) (Combination_product)
Age
Adult, Older Adult · 18+ yrs
Sex
Male
Sponsor
Urotronic Inc.
Primary completion
Oct 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Rate of Treatment Related Serious Complication
SECONDARY
Stricture Recurrence Rate
8 <0.001 sig

Summary

Robust I study is a feasibility study for evaluating the safety and efficacy of DCB.

Eligibility Criteria

Inclusion Criteria

  • Male subjects ≥ 18 years' old
  • Visual confirmation of stricture via cystoscopy or urethrogram
  • Single lesion anterior urethral stricture or bladder neck contracture, less than or equal to 2.0 cm
  • One to three (1-3) prior diagnosis and treatment of the same stricture (including self-catheterization) including DVIU (Direct Vision Internal Urethrotomy), but no prior urethroplasty
  • Significant symptoms of stricture such as frequency of urination, dysuria, urgency, hematuria, slow flow, feeling of incomplete emptying, recurrent UTI's.
  • IPSS score of 13 or higher
  • Lumen diameter <12F by urethrogram
  • Able to complete validated questionnaire independently
  • Qmax <10 ml/sec

Exclusion Criteria

  • Strictures greater than 2.0 cm long.
  • Subjects that have more than 1 stricture.
  • Sensitivity to paclitaxel or on medication that may have negative interaction with paclitaxel
  • Subjects who have a suprapubic catheter and are unable to complete study required testing, such as uroflowmetry
  • Previous urethroplasty within the anterior urethra
  • Stricture due to bacterial urethritis or untreated gonorrhea
  • Stricture dilated or incised within the last 3 months
  • Presence of local adverse factors, including abnormal prostate making catheterization difficult, urethral false passage or fistula.
  • Presence of signs of obstructive voiding symptoms not directly attributable to the stricture such as BPH at the discretion of the clinical investigator
  • Previous radical prostatectomy
  • Previous pelvic radiation
  • Diagnosed kidney, bladder, urethral or ureteral stones or active stone passage in the past 6 months.
  • Diagnosed with chronic renal failure unless under hemodialysis or has a serum creatinine level greater than 2 mg/dL
  • Use of alpha blockers, beta blockers, OAB (Overactive Bladder) medication, anticonvulsants (drugs that prevent or reduce the severity and frequency of seizures), and antispasmodics where the dose is not stable. (Stable dose is defined as having the same medication and dose in the last six months.)
  • Use of Botox (onabotulinumtoxinA) in urinary system within the last 12 months
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03014726). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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