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Active clinical trials for "Urologic Diseases"

Results 81-90 of 147

Intravesical Antifibrinolytic for Patients With Hematuria and Clot Retention

Urologic DiseasesProstate Cancer6 more

A study looking at the feasibility of doing a full-scale RCT that investigates the use of tranexamic acid intravesically prior to continuous bladder irrigation treatment in the emergency department for urinary retention due to clots. We want to know: patient experience and acceptability of the intervention study procedures (recruitment, site appropriateness, staff engagement) safety data identify resource use

Completed12 enrollment criteria

A Novel Robotic System for Single Port and Natural Orifice Transluminal Endoscopic Surgery

Colorectal NeoplasmsUrologic Neoplasms7 more

This is a prospective, single center, multispecialty study that aimed to evaluate the clinical feasibility and safety of single port surgery and NOTES (mainly transanal and transoral surgery) using a novel single port robotic system.

Completed12 enrollment criteria

Pilot Study to Evaluate the Clinical Response to Mitomycin-C in Hydrogel (TC-3) Administered Intravesically...

Urinary Bladder NeoplasmsUrologic Neoplasms3 more

The purpose of this study is to evaluate the clinical response of the tumors within the bladder of recurrent NMIBC patients to Mitomycin-C embedded in UroGen Pharma's (known at that time as TheraCoat Ltd.) TC-3 Sterile Hydrogel (TC-3) and to evaluate the patency of ureters 6 hr post instillation.

Completed14 enrollment criteria

Transcutaneous Electrical Nerve Stimulation (TENS) for Lower Urinary Tract Disorders in Parkinson's...

Parkinson's Disease

Only one study has evaluated the effect of TENS in LUTD in Parkinson's syndromes. It was reported at the congress of the "Société Interdisciplinaire Francophone d'UroDynamique et de Pelvi-Perinéologie" (SIFUD-PP) in 2011 by Ohanessian et al., and comprised 6 female patients with Parkinson's disease (PD) or multisystem atrophy (MSA), with overactive bladder. Transcutaneous electrical nerve stimulation, 20 minutes daily for 6 weeks, was associated with subjective improvement of LUTD assessed with the Patient Global Impression of Improvement (PGI-I) in 5 of the 6 patients. In view of the encouraging results of this pilot study, we hypothesize that TENS treatment may improve LUTD in patients with a Parkinson's syndrome, Parkinson's disease (PD) and multisystem atrophy (MSA).

Completed11 enrollment criteria

A Study of the Safety and Effectiveness of Oral Levofloxacin Compared With Oral Ciprofloxacin in...

Urinary Tract InfectionsBacteriuria3 more

The purpose of the study is to compare the safety and effectiveness of oral levofloxacin (an antibiotic) with that of oral ciprofloxacin in the treatment of complicated urinary tract infections in adults.

Completed8 enrollment criteria

Tamsulosin Phase III Clinical Trial -Double-Blind, Placebo Controlled Study in Female Patients With...

Urinary Tract Diseases

The purpose of this study is to determine whether Tamuslosin is effective in the treatment of lower urinary tract syndrome with female patients.

Completed2 enrollment criteria

Percutaneous Externally-Assembled Laparoscopic Urologic Surgery

Urologic Diseases

This will be a single-arm prospective internally-controlled study. Patients will undergo percutaneous externally-assembled laparoscopic surgery where one or more 3 mm instruments are added or substituted for conventional 5 or 10 mm trocars.

Completed3 enrollment criteria

Dismembered Pyeloplasty With and Without After Coming Stent

Pelviureteric Junction ObstructionPyeloplasty3 more

to compare outcome of pyeloplasty in pediatric population less than 6 months in age using an after coming stent versus stentless pyeloplasty.

Completed10 enrollment criteria

Concealed Penis in Pediatric Age Group

Pediatric ALLSurgery1 more

Background: Comparison between three different surgical techniques in the management of concealed penis. Methods: This prospective interventional non-randomized study included 150 pediatric patients with concealed penis. They were distributed equally into three groups; group A; patients treated by phallopexy only, group B; patients treated by complete dissection and excision of dartos fascia & group C; patients treated by both phallopexy and dartos excision.

Completed2 enrollment criteria

A Study to Evaluate the Efficacy, Safety and Tolerability of Mirabegron and Solifenacin Succinate...

Urologic DiseasesUrinary Bladder Diseases4 more

The purpose of this study is to examine how well two medicines in combination (solifenacin succinate and mirabegron) work in the treatment of bladder problems over a 12-week period.

Completed29 enrollment criteria
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