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Vesicoureteral Reflux clinical trials

View clinical trials related to Vesicoureteral Reflux.

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NCT ID: NCT02786810 Completed - Clinical trials for Urinary Tract Infection

Contrast Enhanced Ultrasound for Evaluation of Reflux Nephropathy

Start date: March 2016
Phase: Phase 2
Study type: Interventional

The study will be evaluating the efficacy and safety of a contrast drug in pediatric renal ultrasound.

NCT ID: NCT02021006 Active, not recruiting - Clinical trials for Chronic Kidney Disease

Antibiotic Prophylaxis and Renal Damage In Congenital Abnormalities of the Kidney and Urinary Tract

PREDICT
Start date: December 2013
Phase: Phase 3
Study type: Interventional

The exact role of urinary tract infection in the appearance of chronic kidney disease is unclear. Children with congenital malformations of kidney and urinary tract have the higher risk of impairment of renal function. To understand if the use of antibiotic prophylaxis can reduce the risk of urinary tract infection in children with these malformations, this study will randomize children in two groups. Group A will not take antibiotic prophylaxis, Group B will take antibiotic prophylaxis for 2 years. This study will assess if antibiotic prophylaxis reduce the risk of urinary tract infections in these children and if urinary tract infections influence the appearance of renal damage. Our hypothesis is that prophylaxis reduce the risk of infection in severe vesicoureteral reflux and that urinary tract infections, in morphologically normal kidneys, will not result in chronic renal failure.

NCT ID: NCT01780493 Completed - Clinical trials for Vesicoureteral Reflux

The Long Term Follow-Up Results Of The Direct Nipple Ureteroneocystostomy Technique

Start date: March 2004
Phase: N/A
Study type: Interventional

To evaluate the long term follow-up results of the direct nipple ureteroneocystostomy technique.

NCT ID: NCT01578291 Terminated - Clinical trials for Vesicoureteral Reflux

Parent Education and Medical Play: A Comparison of Psychological Preparation Strategies for Voiding Cystourethrogram

Start date: December 2011
Phase: N/A
Study type: Interventional

Hypothesis: The use of parent education and medical play will be able to reduce patient discomfort with potential uncomfortable medical procedures. Children that have urinary tract infections and those diagnosed with vesicoureteral reflux undergo a procedure called a voiding cystourethrogram (VCUG) to identify and follow vesicoureteral reflux. For many children and parents this can lead to considerable distress. Pre-procedure preparation can potentially reduce anxiety and improve overall experience with the procedure.

NCT ID: NCT01483105 Completed - Clinical trials for Vesicoureteral Reflux

DVD-Based Training Program in Self-Hypnosis for Children

VCUG
Start date: October 2011
Phase: N/A
Study type: Interventional

The proposed study is designed to utilize a self-hypnosis DVD home-training program for parents to use with their children to teach self-hypnosis techniques for inducing relaxation and hypnotic analgesia. These relaxation techniques can be employed to manage anticipatory anxiety, distress, and pain during an invasive medical procedure, for example, voiding cystourethrography (VCUG). The study will examine the efficacy of this intervention for children undergoing VCUG procedures.

NCT ID: NCT01373385 Completed - Clinical trials for Vesicoureteral Reflux

Prospective Pediatric Vesicoureteral Reflux Surgery Database

Start date: July 2010
Phase: N/A
Study type: Observational

The purpose of this research is to provide a clearer understanding of quality and outcomes for three types of surgical procedures performed at Connecticut Children's for treatment of vesicoureteral reflux. In order to consistently gather data over time, the investigators propose to establish database for surgical intervention for vesicoureteral reflux. Specific Aim 1: To consistently collect performance and outcomes data for the surgical treatment of vesicoureteral reflux in order to increase internal understanding of these procedures. Specific Aim2: To consistently collect performance and outcomes data for the surgical treatment of vesicoureteral reflux in order to perform more valuable clinical analysis for publication.

NCT ID: NCT01137929 Withdrawn - Clinical trials for Vesicoureteral Reflux

Bacterial and Host Genetic Risk Factors in Acute Pyelonephritis

Start date: November 2014
Phase: N/A
Study type: Observational

No single host or pathogen trait identified by previous research can be correlated with all cases of childhood acute pyelonephritis or APN (i.e., kidney/upper urinary tract infections) and APN-associated renal scarring (the outcome with the highest morbidity), making it difficult for physicians to determine which patients will be affected. Our proposal is to comprehensively study the relationships between the clinical manifestations of urinary tract infections (UTIs), the host risk factors and immune response, and the microbial species that cause these conditions. The result of the study will be a clinical severity score to personalize diagnostic and treatment strategies for infants with UTI, with the goal of decreasing the morbidity of APN/renal scarring and improving patient outcomes.

NCT ID: NCT00894465 Terminated - Clinical trials for Vesicoureteral Reflux

Midazolam Effect in Children Undergoing Voiding Cystourethrogram (VCUG)

Start date: August 2006
Phase: N/A
Study type: Interventional

The purpose of this research is to validate the common administration of oral midazolam to children prior to voiding cystourethrogram (VCUG) to see if this will significantly decrease children's anxiety and make the experience less traumatic.

NCT ID: NCT00830479 Withdrawn - Clinical trials for Vesicoureteral Reflux

Study of Endoscopic Versus Open Surgery for Urinary Reflux

STRETCH
Start date: January 2009
Phase: N/A
Study type: Interventional

This study seeks to compare outcomes after anti-reflux surgery (ARS) for correction of low-grade vesicoureteral reflux (VUR). It is a randomized controlled open-label trial of conventional open anti-reflux technique versus endoscopic anti-reflux technique with injection of dextranomer/hyaluronic acid copolymer (Deflux). Primary endpoint will be resolution of VUR at initial cystogram after ARS. Secondary outcomes will include incidence of postoperative UTI, resolution of VUR at 1-year cystogram after ARS, surgical complications, and quality of life measures after ARS.

NCT ID: NCT00815334 Completed - Clinical trials for Vesicoureteral Reflux

Efficacy of Endoscopic Subureteral Injection for Vesicoureteral Reflux in Adults With Decreased Bladder Compliance

Start date: October 2008
Phase: N/A
Study type: Interventional

Endoscopic subureteral injection for vesicoureteral reflux has become an established alternative to ureter reimplantation in children. Some recent studies suggest that ESI can be also a primary treatment option for VUR in adults. However, the experience with ESI in adults who have VUR associated with decreased bladder compliance is limited. We evaluated the efficacy of endoscopic subureteral injection treatment for vesicoureteral reflux in adults with decreased bladder compliance.