Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06795074

Risk of Recurrent Urethral Stricture After Treatment With Paclitaxel-Coated Dilatation Balloon (Optilume) Compared With Non-coated Dilatation Balloon

Urethral strictures are often initially treated endoscopically with dilatation or direct visual internal urethrotomy (DVIU), a procedure where the stricture is incised through the vision of a cystoscope. These methods are easy to perform, they are often well tolerated under local anesthesia and they have a low risk of complications. One disadvantage is the relatively low success rate which is 20-60% when used as a first intervention and considerably lower after several interventions. Instead of repeated endoscopic procedures, it is advisable to perform open urethroplasty. Urethroplasty has a success rate of 65-91% but a higher risk of complications and requires general anesthesia. Therefore, there is a need for a treatment option for recurrent urethral strictures after DVIU or dilatation, before the urethroplasty is performed.

Optilume is a CE-marked paclitaxel-coated dilatation balloon used for treatment of urethral strictures. The industry-sponsored randomised ROBUST III trial from 2022 showed a 75% success rate with Optilume but it is not sure if the results can be generalised to patients who would otherwise be candidates for open urethroplasty and whether the drug coating per se increases the efficacy of balloon dilatation. The aim of this study is to investigate whether the addition of paclitaxel-coating can increase the success rate and decrease the need for additional interventions and open urethroplasty for individuals who has a recurrent urethral stricture following at least one previous endoscopic intervention.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Sahlgrenska University Hospital, Gothenburg, Sweden

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age ≥ 18 years
  • Urethral stricture recurrence after at least one internal urethrotomy or dilatation
  • Penile or bulbar stricture
  • Length of stricture ≤ 2 cm
  • Eligible for open urethroplasty
  • Able to give informed consent

Exclusion criteria

  • Stricture of the meatus
  • Sclerosis of the bladder neck
  • Multiple strictures < 16 Ch
  • Complete stricture without any lumen
  • Previous dilatation with paclitaxel-coated balloon
  • Previous radiation therapy of the pelvis (e.g. for prostate cancer)
  • Previous pelvic fracture
  • Urethral malignancy
  • Presence of urethral fistula
  • Presence of urethral condyloma
  • Previous open urethroplasty
  • Chronic urinary retention secondary to detrusor inactivity

Treatment and study plan

Optilume

Combination Product

Dilatation with drug-coated balloon

UroMax Ultra

Device

Dilatation with non-coated balloon

Primary outcomes

  1. Functional recurrent stricture

    Time frame: Within 18 months of treatment

    Recurrence within 18 months of a functional urethral stricture, defined as:

    • Use of clean intermittent dilatation or
    • Retreatment with dilatation balloon or internal urethrotomy or
    • Need for open urethroplasty or other open procedure

Secondary outcomes

  1. Anatomical recurrent stricture

    Time frame: Within 18 months of treatment

    Anatomical recurrent stricture, defined as impassable with a 16 Fr flexible cystoscope

  2. Qmax

    Time frame: At 6 and 18 months after treatment

    Change in maximum urinary flow after treatment

  3. Time micturition

    Time frame: At 6 and 18 months after treatment

    Change in time micturition (seconds for first 1dL voided urine)

  4. Urethral Stricture Score

    Time frame: At 6, 12 and 18 months after treatment

    Patient reported outcome measure (Urethral Stricture Surgery (USS)-PROM). Score from 0-24, higher indicates worse symptoms. Also includes a quality-of-life question and Peeling's voiding picture.

Study contacts

Contact information is provided by the study sponsor or research team.

Henrik Kjölhede, MD, PhD

CONTACT

[email protected]

+46-31-3421000

Sponsors and collaborators

Lead sponsor

Vastra Gotaland Region

Other Gov

Collaborators

  • Region Skane
  • Region Stockholm
  • Region Örebro

Registry information

Official study title

Risk of Recurrent Urethral Stricture After Treatment With Paclitaxel-Coated Dilatation Balloon (Optilume) Compared With Non-coated Dilatation Balloon - a Prospective Randomised Multicentre Study

Acronym: RUSTIC

Important dates

Study start
2026
Primary completion
2029
Study completion
2031
First posted
Jan 27, 2025
Registry last updated
Jan 16, 2026

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.

Published trials that share one or more normalized conditions with this study.