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Clinical Evaluation of the CM-1500 in Postoperative Surgery Patients

NCT04706221 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2024-03-27

Study results available
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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.

Conditions

  • Blood Loss

Interventions

DEVICE

CM-1500

Blood volume monitor CM-1500

Sponsors & Collaborators

  • Wake Forest University Health Sciences

    collaborator OTHER

  • Zynex Monitoring Solutions

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-01-15
Primary Completion
2021-11-29
Completion
2021-11-29
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04706221 on ClinicalTrials.gov