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Clinical Trials/CTRI/2018/02/011713
CTRI/2018/02/011713
Active, Not Recruiting
Phase 3

Pilot study on using a purpose built device (PreSense) to improve turn-protocol compliance

Healthcare Technology Innovation Centre0 sites40 target enrollmentTBD
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ConditionsHealth Condition 1: null- Pressure Ulcers

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: null- Pressure Ulcers
Sponsor
Healthcare Technology Innovation Centre
Enrollment
40
Status
Active, Not Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Eligibility Criteria

Inclusion Criteria

  • •All adults admitted to Intensive Care Unit (ICU) who are considered at risk of acquiring
  • •pressure ulcers can be enrolled in the study.

Exclusion Criteria

  • •1\. Patients who cannot have the wearable device attached to their chest.
  • •2\. Patients who currently have implantable cardiovascular\- defibrillator or pacemaker.

Outcomes

Primary Outcomes

Not specified

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