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Ambulatory Blood Pressure Measurement in Children With Congenital Urine Flow Obstruction

Expanded access is currently available for this treatment.
Verified October 2008 by University of Texas Southwestern Medical Center
Sponsor:
ClinicalTrials.gov Identifier:
NCT00764543
First Posted: October 2, 2008
Last Update Posted: October 2, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Information provided by:
University of Texas Southwestern Medical Center
  Purpose
Children with unilateral congenital urine flow impairment, who require surgery, have abnormal 24-hour ambulatory blood pressure measurements.

Condition Intervention
Hydronephrosis Multicystic-Dysplastic Kidney Device: 24-hour ambulatory blood pressure monitor

Study Type: Expanded Access     What is Expanded Access?
Official Title: Ambulatory Blood Pressure Measurement in Children With Congenital Urine Flow Obstruction

Resource links provided by NLM:


Further study details as provided by University of Texas Southwestern Medical Center:

Intervention Details:
    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.
  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   up to 24 Months   (Child)
Sexes Eligible for Study:   All
Criteria

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.
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00764543


Contacts
Contact: Warren T. Snodgrass, M.D. 214-456-2483 Warren.Snodgrass@childrens.com

Sponsors and Collaborators
University of Texas Southwestern Medical Center
  More Information

Responsible Party: Warren T. Snodgrass, M.D., University of Texas Southwestern Medical School
ClinicalTrials.gov Identifier: NCT00764543     History of Changes
Other Study ID Numbers: 052005-008
First Submitted: September 30, 2008
First Posted: October 2, 2008
Last Update Posted: October 2, 2008
Last Verified: October 2008

Keywords provided by University of Texas Southwestern Medical Center:
To measure 24-hour ambulatory blood pressure in children who have unilateral hydronephrosis or multicystic-dysplastic kidneys
To compare these blood pressure measurements between the children who require surgical correction and those who do not need surgical correction.

Additional relevant MeSH terms:
Hydronephrosis
Multicystic Dysplastic Kidney
Kidney Diseases
Urologic Diseases
Urogenital Abnormalities
Kidney Diseases, Cystic
Congenital Abnormalities