CompletedNot Applicable

Clinical Evaluation of the CM-1500 in Postoperative Surgery Patients

United States200 participantsStarted 2021-01-15

Plain-language summary

The primary objective is to evaluate the the changes in the Relative Index in post abdominal or pelvic surgery patients on the Cardiac Monitor Model CM-1500.

Who can participate

Age range18 Years – 100 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.

Inclusion Criteria: * Ability to provide written informed consent * Ability and willingness to comply with study procedures and duration requirements * 18 years of age or older * Undergoing an abdominal or pelvic surgery within the next 10 days Exclusion Criteria: * Females who are pregnant or breastfeeding * Participation in other clinical studies involving experimental drugs or devices * Undergone an amputation of the left upper extremity * Diagnosed with Dextrocardia * Subjects who have a Pacemaker

What they're measuring

Relative Index Change During PACU Stay

Timeframe: Length of PACU Stay (Range: 46 to 353 minutes)

Trial details

NCT IDNCT04706221

SponsorZynex Monitoring Solutions

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2021-11-29

Results submitted2023-12-15

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