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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04703582
Other study ID # IIBSP-TCA-2020-92
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date January 2021
Est. completion date June 2021

Study information

Verified date January 2021
Source Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Check whether patients with higher comorbidity and risk of complication, estimated using the V (p) -POSSUM score, ACS NSQIP and the ASA classification, present higher baseline activated clotting time values.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date June 2021
Est. primary completion date March 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients undergoing vascular surgery requiring intraoperative heparinization Exclusion Criteria: - Pregnant women - SARS-CoV-2 PCR positive (performed 24-72h prior to surgery) - Severe plaquetopenia <50,000

Study Design


Intervention

Diagnostic Test:
Activated clotting time
Relationship between elongated baseline activated clotting time and comorbidity

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau

Outcome

Type Measure Description Time frame Safety issue
Primary Change on baseline Activated Clotting Time with comorbidities Activted Clotting Time will be measured with Haemocron Machine just before surgery. Comorbidities will be measured with V(p)Possum, AC NSQUIP and ASA scales. 1 day - surgery day
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