Clinical Trials Directory

Trials / Suspended

SuspendedNCT02778997

Prospective Shunt Complication Study

Prospective Shunt Complication Study (Pro-ShuCS)

Status
Suspended
Phase
Study type
Observational
Enrollment
150 (estimated)
Sponsor
University of Zurich · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Complications in patients with cerebrospinal fluid (CSF) shunts are common. Thus, these patients are frequently admitted for suspicion of a shunt dysfunction (SD). However, the symptoms of a SD are often unspecific and the required diagnostics are time consuming, expensive, invasive and may involve radiation exposure. In a prospective observational study it is planned to find out, how often a suspected shunt dysfunction is found, which kinds of shunt dysfunction are seen and if there is a correlation between the shunt dysfunctions and the age of the shunt. Furthermore, it is intended to find out, if there are symptom-patterns specific for certain shunt dysfunctions.

Detailed description

All patients who are admitted for suspected shunt-dysfunction will be included. Patient data, detailed data about the shunt, patient's symptoms and all findings will be recorded in the CRF. After 4-8 weeks all patients will be followed-up to add missing data and correct initial findings with the benefit of a retrospective view. After 2 years, data will be analyzed.

Conditions

Interventions

TypeNameDescription
PROCEDURECSF Shunt treatment for hydrocephalusState after CSF shunt implantation

Timeline

Start date
2017-04-01
Primary completion
2026-07-01
Completion
2027-07-01
First posted
2016-05-20
Last updated
2025-04-06

Locations

2 sites across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT02778997. Inclusion in this directory is not an endorsement.