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OpenTrials
Completed

NCT Number: NCT01319136

Improved Analysis Methods for Infusion Tests

Objective: Patients with Idiopathic Normal Pressure Hydrocephalus are improved with shunt surgery. To increase the accuracy of the diagnosis, supplementary tests that characterize the cerebrospinal fluid (CSF) dynamics are used. The infusion test is one of these, used for shunt surgery selection and postoperative evaluation of shunt function. Forty-eight patients that had a preoperative investigation because of communicating hydrocephalus at the university hospitals in Umeå and Uppsala, Sweden, participated in the study. The purpose of this study was to evaluate a new method, with a new infusion protocol and new analysis methods, and compare it to the current method.

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Key information

Sex eligibility

All sexes

Study type

Observational

Primary location

Uppsala University Hospital, Uppsala, Uppland, Sweden

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • preoperative investigation because of communicating hydrocephalus
  • ventriculomegaly (Evans ratio > 0.3)
  • no obstruction to CSF flow at visual inspection

Exclusion criteria

  • postoperative infusion test investigations
  • patients that were unable to understand instructions

Sponsors and collaborators

Lead sponsor

Umeå University

Other

Registry information

Official study title

Novel Infusion Method for Describing CSF Dynamics

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Mar 21, 2011
Registry last updated
Mar 21, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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