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Urethral Stricture clinical trials

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NCT ID: NCT06232005 Completed - Urethral Stricture Clinical Trials

Intralesional Injection of Mitomycin C Following Visual Internal Urethrotomy for Recurrent Urethral Stricture

Start date: January 1, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

To evaluate the effectiveness of administering mitomycin C through intralesional injection after performing visual internal urethrotomy (VIU) for the treatment of recurring urethral stricture.

NCT ID: NCT06123520 Completed - Clinical trials for Urethral Stricture, Male

Laser Visual Internal Urethrotomy With Versus Without Paclitaxel Injection

Start date: May 1, 2023
Phase: Phase 3
Study type: Interventional

To evaluate the outcome of visual internal urethrotomy in treating urethral strictures in males with a holmium: yttrium-aluminium garnet (YAG) laser versus when combined with intralesional injection of paclitaxel.

NCT ID: NCT05078788 Completed - Urethral Stricture Clinical Trials

Holmium Laser Uretherotomy in Combination With Intralesional Steroids in Bulbar Uretheral Stricture

Start date: June 2, 2020
Phase: N/A
Study type: Interventional

the purpose is to evaluate the outcome of visual internal uretherotomy with Holmium laser along with intralesional steroid injection.

NCT ID: NCT05069883 Completed - Recurrence Clinical Trials

Role of Oral Steroids in Reducing Recurrence of Urethral Stricture After Direct Vision Internal Urethrotomy

Start date: January 1, 2018
Phase: N/A
Study type: Interventional

It was a randomized controlled trial conducted at department of Urology, Armed Forces Institute of Urology, Rawalpindi from 1st January, 2018 July 2019 to 31st March 2021 to determine the role of oral steroids after Direct Vision Internal Urethrotomy to reduce the recurrence rate of urethral strictures.

NCT ID: NCT04650347 Completed - Clinical trials for Urethral Stricture, Male

Holmium: YAG Versus Cold Knife Internal Urethrotomy in Management of Short Urethral Strictures

Start date: March 1, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

Urethral stricture disease is defined as narrowing of the urethral lumen because of fibrosis, which occurs in urethral mucosa and surrounding tissues. The etiology could be congenital, iatrogenic, infectious, or idiopathic. Several techniques are currently available for minimally invasive treatment of urethral strictures, including cold-knife incision, electrocautery, and various types of laser incisions. An incision with the cold knife does not cause any thermal effect on surrounding tissues but should create a mechanical injury that may lead to recurrence in long term. An incision with the electrocautery should cause a significant thermal effect on healthy surrounding tissues resulting in recurrent strictures during follow-up. Laser treatment modalities have gained popularity in the last two decades. the aim of this trial is to evaluate the safety and efficacy of endo-urethrotomy with Holmium laser and cold knife endo-urethrotomy

NCT ID: NCT04452890 Completed - Clinical trials for Anterior Urethral Stricture, Male

Pre-operative Assessment by Sonourethrography Only in Anterior Urethral Strictures.

PASTIS
Start date: July 1, 2020
Phase: N/A
Study type: Interventional

The choice of the best surgical technique for urethral stricture repair depends on the stricture length. Estimating the length of urethral strictures is therefore of utmost importance. Different clinical studies have proven that SUG has a higher sensitivity to evaluate the length of urethral strictures compared to RUG or VCUG. The goal of this study is to assess the feasibility of using SUG as single pre-operative assessment tool in patients with suspicion of anterior urethral strictures. In this way, use of RUG and/or VCUG could be omitted in the pre-operative work-up of patients with anterior urethral strictures, thereby avoiding significant radiation load of patients.

NCT ID: NCT04357080 Completed - Urethral Stricture Clinical Trials

Factors Predicting Urethral Stricture Recurrence After Dorsal Onlay Augmented, Buccal Mucosal Graft Urethroplasty

Start date: July 15, 2020
Phase:
Study type: Observational

In this observational study, the investigators will evaluate potential risk factors associated with urethral stricture recurrence after augmentation anterior urethroplasty using dorsal onlay buccal mucosal Graft during the past 10 years. Patients' medical files will be reviewed for data relevant to demographics, clinical and operative characteristics. data will be analyzed using the appropriate statistical tests and the independent predictors of urethroplasty outcome will be identified.

NCT ID: NCT04307537 Completed - Urethral Stricture Clinical Trials

Post-Operative Imaging After Urethroplasty With Peri-catheter Retrograde Urethrography Or Trial of Voiding With Voiding Cysto-urethrography

POIROT
Start date: January 21, 2020
Phase: Phase 2
Study type: Interventional

After a reconstructive procedure of the urethra, a transurethral catheter is usually left in place to allow adequate healing of the tissues without exposure to urine. After 7-21 days, depending on several variables (e.g. type of reconstruction, stricture etiology, …), removal of the transurethral catheter is foreseen. However, in order to do so, the clinician first wants to objectify whether the urethra has indeed healed sufficiently and therefore he/she can rely on early postoperative imaging. Up until today, there is no clear standard about when and how to do early postoperative imaging and current practices are mainly based on expert opinion and habit. Basically, two strategies can be found amongst different urethroplasty centers: peri-catheter retrograde urethrography (pcRUG) and voiding cysto-urethrography (VCUG). A pcRUG is performed by placing a small caliber tube (e.g. feeding tube 5 Fr) in the meatus urethrae of the patient, next to the transurethral catheter (which remains in place), and injecting contrast alongside the catheter. With a VCUG, contrast is injected through the transurethral catheter, up to the bladder. Thereafter, the catheter is removed and the patient is asked to urinate and thus to pass contrast through the urethra. The primary end-point of this study is to compare 'the rightful decision to maintain the catheter at the time of imaging' between pcRUG only and pcRUG followed by VCUG in a within-patient fashion.

NCT ID: NCT03973619 Completed - Urethral Stricture Clinical Trials

Urethral Stricture: A Comparison Between Jugal or Labial Graft Urethroplasty

Start date: October 1, 2016
Phase: N/A
Study type: Interventional

Buccal mucosa urethroplasty is a current fashion in urethral stricture management. In our university centre (Hospital de Clínicas de Porto Alegre) is a common surgical treatment choice. This paper aims to evaluate the success rate of this treatment after randomized choice between labial and jugal (inner cheek) grafts during the past two years.

NCT ID: NCT03859024 Completed - Pain, Postoperative Clinical Trials

Efficacy of Opioid-limiting Pain Management Protocol in Men Undergoing Urethroplasty

Start date: March 22, 2019
Phase: Phase 4
Study type: Interventional

The investigator's study aims to see if an enhanced recovery regimen of pain medications before and during surgery will decrease the use and risk of opioid pain medications as well as improve pain control in anterior urethroplasty patients. Participants will be randomized to one of two pain regimens (enhanced recovery regimen vs standard regimen).