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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | CSF Shunt treatment for hydrocephalus | State 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.