Last reviewed · How we verify

NCT05806762

Prediction of Rehospitalization Following a Sepsis Admission Using a Wearable Biopatch

Recruiting now Last updated 3 April 2024
What this trial tests

trial testing BioIntellisense in Sepsis in 200 participants. Currently enrolling.

Timeline
1 May 2023
Primary endpoint
1 May 2027
2 May 2027

Quick facts

Lead sponsorUniversity of California, San Diego
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment200
Start date1 May 2023
Primary completion1 May 2027
Estimated completion2 May 2027
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of California, San Diego

Who can join

18 and older, any sex, with Sepsis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this observational study is to learn about the utility of biopatches predicting 30-day readmissions in patients discharged from the hospital with sepsis. The main question\[s\] it aims to answer are: • Does the application of a biopatch provide data that can improve prediction of an unplanned 30-day readmission following a hospitalization for sepsis. Participants will be asked to wear a biopatch on their chest for 30-days following hospital discharge or until readmission to the hospital.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Sepsis

Currently open trials in the same condition.

Other University of California, San Diego 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/NCT05806762.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing