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Completed

NCT Number: NCT03014726

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

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

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Early Phase 1

Primary location

Libra Medical Inc

Brooklyn Park, Minnesota, 55428, United States

About this study

The study is designed to determine the safety and effectiveness for drug coated balloon (DCB).

Up to 50 subjects is planned to be enrolled and treated with the study device at up to 5 clinical sites outside of US. Due to significantly higher prevalence of strictures in men vs. women and the etiology of those strictures being different, the study will focus on male subjects with single anterior urethral stricture. Subjects will be followed up post-treatment to one year and then annually for up to 5 years. The annual follow up after the first year is optional.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Urotronic Drug Coated Balloon (DCB)

Combination Product

Urotronic Drug Coated Balloon (DCB) is a catheter with a tapered atraumatic tip. The distal end of the catheter has a semi-compliant inflatable balloon coated with a proprietary coating containing the drug and carriers.

Primary outcomes

  1. Rate of Treatment Related Serious Complication

    Time frame: 90 days post-procedure

    • urethral formation of fistula
    • de novo severe urinary retention lasting > 14 consecutive days' post-treatment
    • unresolved de novo stress urinary incontinence (requiring >1 pad/day) at 90 days or earlier
    • urethra rupture or burst.

Secondary outcomes

  1. Stricture Recurrence Rate

    Time frame: 90 days post-procedure

    • IPSS score of greater than 11 at the 90-day follow-up, or
    • if a subject had a second DCB treatment (retreatment), or
    • if a subject exited the study early due to treatment failure (IPSS >11 without cystoscopically confirmed anatomical success at the time of exit or receiving additional stricture treatment with an alternative therapy).

Sponsors and collaborators

Lead sponsor

Urotronic Inc.

Industry

Registry information

Official study title

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

Acronym: ROBUST

Important dates

Study start
2016
Primary completion
2018
Study completion
2023
First posted
Jan 9, 2017
Registry last updated
Mar 22, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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