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NCT06629168
The Usage of Telemetric Prechamber Sensor Reservoir in Management of Normal Pressure Hydrocephalus. Comparisson of Benefit for Patients with Implanted Telemetric Prechamber Sensor Reservoir.
trial testing lumbar puncture in Hydrocephalus in 33 participants. Completed in 31 December 2024.
31 October 2024
Quick facts
| Lead sponsor | University Hospital Hradec Kralove |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 33 |
| Start date | 1 January 2018 |
| Primary completion | 31 October 2024 |
| Estimated completion | 31 December 2024 |
| Sites | 1 location across Czechia |
Drugs / interventions tested
- lumbar puncture — full drug profile →
- External lumbar drainage
- Ventriculo-peritoneal shunt placement
- Follow-up control #1
- Follow-up control #2
- Follow-up control #3
- Follow-up control #4
- Telemetric prechamber reading
- Valve setting change
Conditions studied
- Hydrocephalus — all drugs for Hydrocephalus →
- Normal Pressure Hydrocephalus — all drugs for Normal Pressure Hydrocephalus →
- Normal Pressure Hydrocephalus Patients — all drugs for Normal Pressure Hydrocephalus Patients →
Sponsor
University Hospital Hradec Kralove
Who can join
40 and older, any sex, with Hydrocephalus or Normal Pressure Hydrocephalus. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Normal pressure hydrocephalus (NPH) is a preventable and treatable cause of dementia. However, as a nosological entity, it is significantly underdiagnosed, often being mistakenly classified as presenile or senile dementia without further investigation. Ongoing management is crucial, currently relying mainly on indirect methods-clinical and imaging-based. Telemetry offers a real-time, online method to assess actual cerebrospinal fluid pressures, which are crucial for patient management. Telemetry allows for tailoring treatment to the individual patient. This project is planned as a pilot study before a more extensive research project.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06629168
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Currently open trials in the same condition.
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Other University Hospital Hradec Kralove trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06629168 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University Hospital Hradec Kralove
- Last refreshed: 23 January 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06629168.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing