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Prospective Shunt Complication Study

Prospective Shunt Complication Study (Pro-ShuCS)

Status
Suspended
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02778997
Acronym
ShuCS
Enrollment
150
Registered
2016-05-20
Start date
2017-04-01
Completion date
2027-07-01
Last updated
2025-04-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Shunt; Complications, Ventricular (Communicating)

Keywords

Shunt, CSF, Dysfunction, Complication

Brief 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.

Interventions

PROCEDURECSF Shunt treatment for hydrocephalus

State after CSF shunt implantation

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \>= 18 * State after implantation of a CSF shunt

Exclusion criteria

* refusion participation in the study

Design outcomes

Primary

MeasureTime frameDescription
Confirmation of Shunt Dysfunction (yes/no)4-8 weeks after first presentationThe correctness of the suspected diagnosis of a shunt dysfunction
Kind of Shunt Dysfunction (infection/disruption/kinking/obstruction/others)4-8 weeks after first presentationIn case of a confirmed shunt dysfunction, the kind of dysfunction is recorded
Alternate Diagnosis (multiple diagnoses possible)4-8 weeks after first presentationIf the suspected diagnosis of a shunt dysfunction is not approved, the alternate diagnosis leading to the patient's symptoms is recorded. Every possible medical disorder might lead to presentation of the patient. Thus, no catalogue of possible diagnoses is given.
Time Span after Shunt Implantation (months)4-8 weeks after first presentationCertain kinds of shunt dysfunctions seem to appear at a certain age of a shunt. The time after implantation/last revision of the shunt is recorded. The age of the shunt / time span after first implantation is measured in months.

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026