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APD Perfusion Measurement Study

APD Perfusion Measurement Study - To test safety and performance of APD devices to measure gut perfusion

Status
Unknown
Phases
Phase 2
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35764
Enrollment
5
Registered
2012-08-10
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

gut perfusion Blood flow in the gut. Gut mucosa perfusion

Interventions

None listed

Sponsors

CMI GMBH
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients for elective sugery for repair of infrarenal abdominal aneurysm

Exclusion criteria

Exclusion criteria: ASA classification IV or V Malignancy Uncontrollable hypertension systolic > 240 mmHg or diastolic > 110 mmHg Uncontrollable heart failure

Design outcomes

Primary

MeasureTime frame
A device developed to determine the intestinal mucosa blood flow, measured in ml / min—

Secondary

MeasureTime frame
None.—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)