Vesico-Ureteral Reflux Clinical Trial
Official title:
A Prospective Study Comparing the Success Rate of Injection of Dextranomer /Hyaluronic Acid (DefluxR) Versus Polyacrylate Polyalcohol (VantrisR) for Treatment of Bilateral Similar Grade Vesicoureteral Reflux in Children
Vesicoureteral reflux (VUR) is the most common urologic diagnosis in neonates estimated at
1% of newborns, and 30-45% of the children who present with urinary tract infection (1).
Optional treatments of children with VUR include conservative therapy with or without
prophylactic antibiotics, and endoscopic, laparoscopic, or open surgery.
In an endoscopic technique, the injecting needle is inserted through the working channel of
the cystoscope. The procedure is relatively short and is performed as out-patient surgery.
In 2000, Dextranomer/Hyaluronic acid (DefluxR) was approved by the FDA, and subsequently has
become the treatment of choice in VUR grades 2-4.
In 2004, the hydrodistention-implantation technique (HIT) was introduced by Kirsch. HIT
involves the use of a pressurized stream of fluid directed into the ureter to aid
visualization, and injection into the submucosa within the ureteric tunnel to improve
coaptation of the ureter (3).
One of the disadvantages attributed to Deflux is the loss of 20% of the injected material
over time (a result of absorption of the hyaluronic acid), which may explain the lower
success rate of the endoscopic treatment of VUR compared with open surgery.
In 2005, Polyacrylate Polyalcohol (VantrisR), a non- absorbable chemical preparation was
introduced for endoscopic treatment of VUR, aiming to improve on the results of Deflux by
preventing volume loss. Preliminary results of a three year follow-up using Vantris have
shown high a level of reflux resolution(4).
The aim of the current study is to compare the rate of resolution of the VUR using Deflux
versus Vantris in bilateral VUR
Status | Recruiting |
Enrollment | 100 |
Est. completion date | December 2015 |
Est. primary completion date | October 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 1 Year to 18 Years |
Eligibility |
Inclusion Criteria: - Bilateral VUR of the same grade Exclusion Criteria: - Inability to apply the same technique on both ureteral orifices |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Israel | Schneider Medical Center of Israel | Petach Tikva |
Lead Sponsor | Collaborator |
---|---|
Rabin Medical Center |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | rate of resolution of VUR using Vantris vs.Deflux | 2 years | Yes |
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