- Our Services
-
Patients and Families
- Get Directions
- Parking
- Childrens Locations
- Getting Around
- Guidelines for Visitors
- Contact a Patient
- Contact Children's
- Send an e-Card
- Gift Shop
Planning a Visit
- Find a Doctor
- Child Health A-Z
- Community Ed.Classes
- Injury Prevention
- International Patients
- Medical Records
- Patient Handbook
- Patient Procedures
Parents
- For Health Professionals
- Research
- Ways to Give
-
News
-
Adding Breast Milk Ingredient to Formula Could Prevent Deadly Intestinal Problem in Premature Babies
-
Children's Holds Groundbreaking Ceremony for Expansion to New South Fayette Location
-
Child Neurodevelopmental and Mental Health Disabilities on the Rise, Study Finds
News Releases
-
Research
Hydrocephalus Shunting Outcomes Review
Shunting Outcomes of Post-Hemorrhagic Hydrocephalus
Protocol Description
This multi-center research study examines the ways in which infants were treated for intraventricular hemorrhage (IVH) and hydrocephalus, also known as post-hemorrhagic hydrocephalus (PHH). Through the program, researchers will compile a comprehensive database about babies diagnosed with and treated for PHH. This is a project of the Hydrocephalus Clinical Research Network, a collaboration of pediatric neurosurgery centers in North America.
Eligibility Criteria
This study is open to infants of both genders up to 180 days of age who have been diagnosed with PHH, which may require treatment through shunting.
Newborns: Up to 180 days old
Newborns: Up to 180 days old
Requirements
Participation in the study will not change any clinical, surgical or imaging routines required for the child’s treatment. Parents will be asked for permission to allow the placement of their child’s past, current and future medical record information into the study database, along with copies of medical images taken as part of the treatment and information about surgery and outcomes, for up to 6 months after a procedure is done.
Visits: None beyond standard treatment
Duration: Not applicable
Participation in the study will not change any clinical, surgical or imaging routines required for the child’s treatment. Parents will be asked for permission to allow the placement of their child’s past, current and future medical record information into the study database, along with copies of medical images taken as part of the treatment and information about surgery and outcomes, for up to 6 months after a procedure is done.
Visits: None beyond standard treatment
Duration: Not applicable
Status: Open for Enrollment
Source(s) of Support
Hydrocephalus Clinical Research Network
National Institutes of Health
Hydrocephalus Clinical Research Network
National Institutes of Health
Primary Investigator(s)
Mandeep Tamber, MD, PhD
Contact Information
For information, please contact:
Arlene M. Luther, BS, RN
412-692-9965
Last Update
April 26, 2011
April 26, 2011
