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NCT05906355

Primary Clinical Evaluation of Wearable Filtrating Artificial Kidney Device for On-site Medical Rescue

Status unknown NA Last updated 15 June 2023
What this trial tests

NA trial testing the wearable filtrating artificial Kidney Device in Fluid Overload in 12 participants. Status unknown.

Timeline
25 June 2023
Primary endpoint
31 October 2025
31 December 2025

Quick facts

Lead sponsorChinese PLA General Hospital
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment12
Start date25 June 2023
Primary completion31 October 2025
Estimated completion31 December 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Chinese PLA General Hospital

Who can join

Adults 18 to 70, any sex, with Fluid Overload. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Fluid overload is a common feature of diseases such as heart failure and kidney injury, which can lead to pulmonary edema or even death if not treated in time. In order to rapidly relieve fluid overload in patients, a wearable filtrating artificial kidney device was developed. The purpose of this study is to evaluation of the precision, security, and operability of wearable filtrating artificial kidney device for on-site medical rescue.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Fluid Overload

Currently open trials in the same condition.

Other Chinese PLA General Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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/NCT05906355.

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