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Hydronephrosis clinical trials

View clinical trials related to Hydronephrosis.

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NCT ID: NCT03296280 Completed - Heart Failure Clinical Trials

Evaluation of Implementation of a National Point-of-Care Ultrasound Training Program

Start date: October 3, 2016
Phase:
Study type: Observational

This VA QUERI Partnered Evaluation Initiative will evaluate the impact of an immersive Point-of-care Ultrasound (POCUS) Training Course on provider skill acquisition and retention; the frequency of POCUS use by trained providers; and the barriers/facilitators to POCUS in the VHA. Data sources include pre- and post-course assessment tools, medical coding data, and course evaluations. Providers that participate in the POCUS Training Course will be compared to control providers from wait-listed facilities. Additionally, participating facilities vs. wait-listed facilities for the POCUS Training Course will be compared. Findings from this project will guide ongoing efforts of the investigators' operating partners, VA Specialty Care Centers of Innovation (SCCI) and the VA Simulation Learning and Research Network (SimLEARN), to develop a national POCUS training program and facilitate implementation of POCUS use system-wide in the VA healthcare system.

NCT ID: NCT02976870 Completed - Hydronephrosis Clinical Trials

Hydronephrosis After Anterior Lumbar Interbody Fusion (ALIF)

HAALIF
Start date: November 2012
Phase: N/A
Study type: Interventional

Anterior lumbar spinal surgery involves making an incision through the abdomen of the patient in order to access the spine. During this process, several internal structures are pushed aside in order to gain access. One of these structures is the ureter, whose function is to drain urine from the kidney to the bladder. One potential complication that can arise from this is dilation of the kidney - known as hydronephrosis. The aim of this study is to identify whether hydronephrosis after Anterior Lumbar Interbody Fusion (ALIF) is complication, in order to bring this to the attention of health care professionals when considering this kind of surgery.

NCT ID: NCT02929160 Withdrawn - Sepsis Clinical Trials

Percutaneous Nephrostomy Versus Stent In Sepsis Trial

PERSIST
Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Randomized control trial to compare the efficacy and safety of percutaneous nephrostomy with retrograde ureteric stenting for emergency renal decompression in cases of obstruction and sepsis associated with ureteric calculi.

NCT ID: NCT02825485 Terminated - Clinical trials for Post-natal Hydronephrosis

Minimizing the Utilization of Voiding Cystourethrography for Patients With Antenatal Hydronephrosis

Start date: July 27, 2016
Phase: N/A
Study type: Interventional

It has previously been found that there is no correlation between degree of hydronephrosis and presence of reflux; however this is oftentimes the criteria physicians use to obtain a VCUG.

NCT ID: NCT02812420 Active, not recruiting - Hydronephrosis Clinical Trials

Durvalumab and Tremelimumab in Treating Patients With Muscle-Invasive, High-Risk Urothelial Cancer That Cannot Be Treated With Cisplatin-Based Therapy Before Surgery

Start date: March 7, 2017
Phase: Early Phase 1
Study type: Interventional

This pilot phase I trial studies the side effects of durvalumab and tremelimumab in treating patients with muscle-invasive, high-risk urothelial cancer that cannot be treated with cisplatin-based therapy before surgery. Immunotherapy with monoclonal antibodies, such as durvalumab and tremelimumab, may induce changes in the body's immune system and may interfere with the ability of tumor cells to grow and spread.

NCT ID: NCT02812212 Recruiting - Clinical trials for Ureteropelvic Junction Obstruction

CTT on Renogram as an Early Marker of Significant Obstruction in Uretero-pelvic Junction Syndrome

JUMP
Start date: November 28, 2017
Phase: N/A
Study type: Interventional

Cortical transit time on diuretic renogram as an early marker of significant obstruction in antenatally detected uretero-pelvic junction syndrome

NCT ID: NCT02713633 Terminated - Clinical trials for Ureteropelvic Junction Obstruction

Indwelling Double-J Ureteral Stent Versus Externalized Modified-Salle Stent for Pyeloplasty

Start date: January 2016
Phase: N/A
Study type: Interventional

This prospective study, Randomized Trial of Indwelling Double-J Ureteral Stent Versus Externalized Modified-Salle Stent for Pyeloplasty will consist of four steps: 1.) Enrolling subjects in the study and signing the consent form 2.) Randomly divide subjects into 2 groups, group 1 will have internal stent and group 2 will have external stent 3.) At the time of stent removal in the clinic or in the OR subjects parents/ subjects will fill a questionnaire about pain after the procedure, stent care and stent tolerance and 4) Data from the questionnaires and procedure cost will be collected and all the data will be analyzed

NCT ID: NCT02276924 Completed - Nephrolithiasis Clinical Trials

Diagnostic Relevance of Laser Confocal Microscopy for the Screening of Upper Urinary Tract Tumors

UROVISIO
Start date: October 2013
Phase: N/A
Study type: Interventional

Upper Urinary Tract Tumors have an incidence of 1 to 2 cases for 100 000 persons per year. The standard treatment for these tumors is the ablation of the kidney, ureter and a part of the bladder surrounding the ureteral orifice. The development of new diagnosis and treatment techniques through natural routes opens the possibility to use conservative treatments. The investigators hypothesis is that during a reno-ureteroscopy, laser confocal microscopy will allow the discrimination between normal and pathologic urothelium by microscopic analysis. This will prevent the systematic use of biopsies which are often difficult and iatrogenic.

NCT ID: NCT02140970 Completed - Urolithiasis Clinical Trials

Randomized Trial of NSAID vs Placebo Prior to Ureteral Stent Removal

Start date: May 2014
Phase: N/A
Study type: Interventional

This study plans to learn more about whether ibuprofen can reduce pain after removal of a ureteral stent more than a placebo. Some patients experience pain after removal of a ureteral stent. The investigators plan to learn how often this occurs and whether it can be prevented. The investigators hypothesize that children who have a temporary, indwelling ureteral stent will experience a significantly less post-operative pain if given a non-steroidal anti-inflammatory (NSAID) prior to removal of the ureteral stent when compared to placebo. The investigators hypothesize that the incidence of severe post-stent removal pain is similar to an adult population.

NCT ID: NCT02138877 Completed - Clinical trials for Obstructive Uropathy

Dismembered Pyeloplasty With and Without After Coming Stent

Start date: January 2014
Phase: N/A
Study type: Interventional

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