Simplified Diagnostic Algorithm for Evaluation of Neonates With Prenatally Detected Hydronephrosis
1 other identifier
observational
76
1 country
1
Brief Summary
Patients with congenital hydronephrosis will be identified by inpatient consultations performed by Dr. Assadi for congenital hydronephrosis and by outpatient problem lists with congenital hydronephrosis of Dr. Assadi's existing patients. Given standard evaluation will be evaluated to determine if based on initial ultrasound classification an algorithm can be developed to target evaluation studies for the initial evaluation. With a goal of targeting the few children that have need of additional intervention and minimizing the studies performed on children who will spontaneously resolve.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2005
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2005
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2010
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2010
CompletedFirst Submitted
Initial submission to the registry
April 1, 2011
CompletedFirst Posted
Study publicly available on registry
April 7, 2011
CompletedApril 7, 2011
April 1, 2011
5 years
April 1, 2011
April 5, 2011
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
surgical intervention required
Primary outcome will be progressive renal function decline and progression to referral to a pediatric urologist for pyeloplasty.
Follow for minimum 1 year, approximately 2 years goal
Study Arms (4)
Bilateral Hydronephrosis Grade I-II
Patients with Bilateral Hydronephrosis Grade I-II
Bil. Hydronephrosis Grade III-IV, Other
Patient with Bilateral Hydronephrosis Grade III-IV and others with any hydronephrosis and distended bladder or MCKD
Unilateral Hydronephrosis Grade I-II
Patients with Unilateral Hydronephrosis Grades I-II
Unilateral Hydronephrosis Grade III-IV
Patients with Unilateral Hydronephrosis Grade III-IV
Eligibility Criteria
Infants with prenatally diagnosed hydronephrosis by ultrasound who have consulted pediatric nephrology
You may not qualify if:
- prior history of UTI
- diagnosis of cystic renal dysplasia with poorly functioning kidney
- previous operation on the urinary tract system
- and other deformities of the external genital organs or anomalies in cardiopulmonary and central nervous system
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Rush University Medical Center
Chicago, Illinois, 60612, United States
Related Publications (25)
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PMID: 20148340BACKGROUNDArdissino G, Dacco V, Testa S, Bonaudo R, Claris-Appiani A, Taioli E, Marra G, Edefonti A, Sereni F; ItalKid Project. Epidemiology of chronic renal failure in children: data from the ItalKid project. Pediatrics. 2003 Apr;111(4 Pt 1):e382-7. doi: 10.1542/peds.111.4.e382.
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PMID: 1432172BACKGROUNDHerndon CD, McKenna PH, Kolon TF, Gonzales ET, Baker LA, Docimo SG. A multicenter outcomes analysis of patients with neonatal reflux presenting with prenatal hydronephrosis. J Urol. 1999 Sep;162(3 Pt 2):1203-8. doi: 10.1016/S0022-5347(01)68134-5.
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PMID: 16362721BACKGROUNDEstrada CR, Peters CA, Retik AB, Nguyen HT. Vesicoureteral reflux and urinary tract infection in children with a history of prenatal hydronephrosis--should voiding cystourethrography be performed in cases of postnatally persistent grade II hydronephrosis? J Urol. 2009 Feb;181(2):801-6; discussion 806-7. doi: 10.1016/j.juro.2008.10.057. Epub 2008 Dec 17.
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PMID: 14654029BACKGROUNDMaizels M, Alpert SA, Houston JT, Sabbagha RE, Parilla BV, MacGregor SN. Fetal bladder sagittal length: a simple monitor to assess normal and enlarged fetal bladder size, and forecast clinical outcome. J Urol. 2004 Nov;172(5 Pt 1):1995-9. doi: 10.1097/01.ju.0000142136.17222.07.
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PMID: 20650499BACKGROUND
Study Officials
- PRINCIPAL INVESTIGATOR
Farahnak Assadi, MD
RUSH University, Pediatrics, Nephrology
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
April 1, 2011
First Posted
April 7, 2011
Study Start
January 1, 2005
Primary Completion
January 1, 2010
Study Completion
January 1, 2010
Last Updated
April 7, 2011
Record last verified: 2011-04