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Urethral Stricture clinical trials

View clinical trials related to Urethral Stricture.

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NCT ID: NCT03014726 Completed - Stricture Urethra Clinical Trials

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

ROBUST
Start date: November 2016
Phase: Early Phase 1
Study type: Interventional

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

NCT ID: NCT02948842 Completed - Urethral Stricture Clinical Trials

Clostridium Histolyticum Collagenase Injection for Urethral Disease

Start date: May 22, 2020
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy of clostridium histolyticum collagenase (XIAFLEX®) in treating urethral strictures.

NCT ID: NCT02634619 Terminated - Urethral Stricture Clinical Trials

A Study of Dorsal Versus Ventral Buccal Mucosa Graft Onlay for Bulbar Urethroplasty

DvV
Start date: June 2016
Phase: N/A
Study type: Interventional

The investigators propose a randomized non-blinded comparison of dorsal vs. ventral approach for buccal mucosa graft urethroplasty in the bulbar urethra. Buccal mucosa graft is a common method of repairing the strictured urethra. Current evidence suggests the two approaches for placement of the graft are equally successful at correcting the stricture and the two approaches have similar risks of complications. The investigators propose to randomly assign appropriately selected patients to either a dorsally- or ventrally-placed graft. No additional procedures beyond normal care protocol will be required of the patients. Success will be assessed via objective and subjective methods; complications will be tallied in a standardized fashion. Outcomes will be measured at two years.

NCT ID: NCT02551783 Terminated - Urethral Stricture Clinical Trials

Dorsal vs. Ventral Buccal Graft Dorsal vs. Ventral Buccal Graft

DoVeBuG
Start date: September 1, 2015
Phase: N/A
Study type: Interventional

This is a randomized non-blinded comparison of dorsal vs. ventral approach for buccal mucosa graft urethroplasty in the bulbar urethra. Buccal mucosa graft is a common method of repairing the strictured urethra. Current evidence suggests the two approaches for placement of the graft are equally successful at correcting the stricture and the two approaches have similar risks of complications. The investigators propose to randomly assign appropriately selected patients to either a dorsally- or ventrally-placed graft. No additional procedures beyond the normal care protocol will be required of the patients. Success will be assessed via objective and subjective methods; complications will be tallied in a standardized fashion. Outcomes will be measured at two years.

NCT ID: NCT02321670 Completed - Urethral Stricture Clinical Trials

Scandinavian Urethroplasty Study

SUPS
Start date: September 2015
Phase: N/A
Study type: Interventional

A multicentre, prospective, randomized study comparing bulbar urethroplasty with excision and primary anastomosis or with an onlay grafting procedure using buccal mucosa.

NCT ID: NCT01982136 Completed - Urethral Stricture Clinical Trials

Functional Outcome of Urethral Reconstructive Surgery

Start date: August 2009
Phase:
Study type: Observational [Patient Registry]

The analysis of the long-term outcomes and quality-of-life parameters after urethral reconstruction surgery.

NCT ID: NCT01889888 Enrolling by invitation - Clinical trials for Urethral Strictures in Males

Effectiveness and Safety of Autologous Adipose-Derived Regenerative Cells for the Treatment of Urethral Strictures

Start date: June 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Autologous adipose-derived regenerative cells (ADRC) extracted using Celution 800/CRS System (Cytori Therapeutics Inc)from a portion of the fat harvested from the patient's front abdominal wall. ADRC will be administered one-time endoscopically into submucosal layer of urethra under eye control into the stricture site after mechanical dilation. This is a single arm study with no control. All patients receive cell therapy.

NCT ID: NCT01790776 Withdrawn - Clinical trials for Urethral Stricture Disease

Diagnosis of Urethral Stricture With Sono-urethrography vs Conventional Urethrography (SONO-URETHRA)

SONO-URETHRA
Start date: February 2013
Phase: Phase 3
Study type: Interventional

Conventional urethrography is the standard diagnostic evaluation for patients with a suspicion of urethral stricture. The radiation dose of this examination is 5-9 mSV. Sono-urethrography was introduced in 1988 (McAninch et al. , J Urol 1988); the diagnostic accuracy of sono-urethrography is equal compared to conventional urethrography, with even a better measurement of stricture length and degree of spongiofibrosis with sono-urethrography. However, sono-urethrography remained underused among urologists and radiologists. Patients will be randomly assigned into two groups: Group A: conventional urethrography Group B: sono-urethrography In case sono-urethrography is inconclusive or of poor quality, a conventional urethrography will be performed. The radiation dose in the two groups will be measured. The stricture length and location will be recorded and compared with the perioperative findings in order to evaluate the diagnostic accuracy. The complications of the procedure(s) will be recorded with a questionnaire directly after and two weeks after the conventional or sono-urethrography.

NCT ID: NCT01214525 Completed - Clinical trials for Urethral Meatal Stenosis

The Improvement in Uroflow and Postvoid Residual Urine After Urethral Meatotomy in Children With Meatal Stenosis

Start date: October 2010
Phase:
Study type: Observational

The improvement in uroflow and postvoid residual urine in children after urethral meatotomy for meatal stenosis. The hypothesis is that there is an improvement in both parameters, thus justifying the procedure.

NCT ID: NCT01196572 Recruiting - Urethral Strictures Clinical Trials

Efficiency of Cold vs. Laser Internal Urethrotomy Treatment of Urethral Strictures

IU
Start date: September 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether laser internal urethrotomy (IU) is as efficient as cold knife internal urethrotomy for treatment of anterior urethral strictures regarding post operative urination outflow, stricture recurrence rate and possible post- operative complications