At a glance
ClinicalIndex Comparison RecordN/ACompleted· 200 enrolled
Drug / intervention
CM-1500device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Clinical Evaluation of the CM-1500 in Postoperative Abdominal and Pelvic Surgery Patients
In Brief
A clinical study evaluating CM-1500 for Blood Loss. Completed, enrolled 200 participants across 1 site.
Detailed 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.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsBlood Loss
CountriesUnited States
CollaboratorsWake Forest University Health Sciences
Timeline
N/ACompletedFinished
202120222023202420252026
First PostedJan 2021
Enrollment StartJan 2021
Primary CompletionNov 2021
TodayJul 2026
First PostedJan 12, 2021
Enrollment StartJan 15, 2021
Primary CompletionNov 29, 2021
TodayJul 2, 2026
Enrollment to primary: 10 monthsPosted 5.5 years ago
Interventions
CM-1500device
Blood volume monitor CM-1500