CompletedNot Applicable

AMS Evaluation Study

United Kingdom34 participantsStarted 2021-02-26

Plain-language summary

A study to evaluate the operational and functional features of the Ambulatory Monitor Solution (AMS) as well as the ease of use of the system.

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

✕. Have previously participated in this study (no subject may participate more than once);
✕. Have an implantable pacemaker;
✕. Diagnosed with infection requiring isolation; OR
✕. Known to be pregnant and/or breast feeding;

User feedback survey about the use of the Ambulatory Monitoring Solution

Timeframe: 5 days

NCT IDNCT04472208

SponsorGE Healthcare

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2021-10-14