Ambulatory Blood Pressure Measurement in Children With Congenital Urine Flow Obstruction

The recruitment status of this study is unknown because the information has not been verified recently.
Verified October 2008 by University of Texas Southwestern Medical Center.
Recruitment status was  Available
Sponsor:
Information provided by:
University of Texas Southwestern Medical Center
ClinicalTrials.gov Identifier:
NCT00764543
First received: September 30, 2008
Last updated: October 1, 2008
Last verified: October 2008

September 30, 2008
October 1, 2008
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Complete list of historical versions of study NCT00764543 on ClinicalTrials.gov Archive Site
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Ambulatory Blood Pressure Measurement in Children With Congenital Urine Flow Obstruction
Ambulatory Blood Pressure Measurement in Children With Congenital Urine Flow Obstruction

Children with unilateral congenital urine flow impairment, who require surgery, have abnormal 24-hour ambulatory blood pressure measurements.

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Expanded Access
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  • Hydronephrosis
  • Multicystic-Dysplastic Kidney
Device: 24-hour ambulatory blood pressure monitor
Patients will go home with the 24-hour ambulatory blood pressure monitor to be returned at the clinic after 24 hours.
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
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Inclusion Criteria:

  • Children of all races and both sexes including Spanish-speaking under 24 months of age with unilateral hydronephrosis greater than 10-mm in anterior posterior diameter; multicystic-dysplastic kidney on ultrasound examination.

Exclusion Criteria:

  • Children over 24 months of age who have undergone surgery and whose parents do not wish to be involved in the study.
Both
up to 24 Months
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Contact: Warren T. Snodgrass, M.D. 214-456-2483 Warren.Snodgrass@childrens.com
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NCT00764543
052005-008
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Warren T. Snodgrass, M.D., University of Texas Southwestern Medical School
University of Texas Southwestern Medical Center
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University of Texas Southwestern Medical Center
October 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP