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

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age18+
SponsorVastra Gotaland Region

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years

Urethral stricture recurrence after at least one internal urethrotomy or dilatation

Penile or bulbar stricture

Length of stricture ≤ 2 cm

Disqualifiers

Stricture of the meatus

Sclerosis of the bladder neck

Multiple strictures < 16 Ch

Complete stricture without any lumen

Trial design

Design model

Parallel

Treatments tested in this trial

  • Optilume

    Combination product

    Dilatation with drug-coated balloon

  • UroMax Ultra

    Device

    Dilatation with non-coated balloon

Treatment groups

230 Participants
are divided into 2 treatment groups
Group A: Paclitaxel-coated dilatation ballonExperimental treatment 1 intervention
Group B: Non-coated dilatation balloonActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Functional recurrent stricture

Recurrence within 18 months of a functional urethral stricture, defined as: 1. Use of clean intermittent dilatation or 2. Retreatment with dilatation balloon or internal urethrotomy or 3. Need for open urethroplasty or other open procedure

Time frame
Within 18 months of treatment

Secondary outcomes

1

Anatomical recurrent stricture

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

Time frame
Within 18 months of treatment
2

Qmax

Change in maximum urinary flow after treatment

Time frame
At 6 and 18 months after treatment
3

Time micturition

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

Time frame
At 6 and 18 months after treatment
4

Urethral Stricture Score

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.

Time frame
At 6, 12 and 18 months after treatment

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Vastra Gotaland Region

Lead sponsor

Region Skane

Collaborator

Region Stockholm

Collaborator

Region Örebro

Collaborator