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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02041403
Other study ID # CE ICH-158/12
Secondary ID
Status Completed
Phase N/A
First received January 18, 2014
Last updated January 21, 2014
Start date June 2012
Est. completion date July 2013

Study information

Verified date January 2014
Source Istituto Clinico Humanitas
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Observational

Clinical Trial Summary

An observational trial aiming to verify whether does any relationship exist between renal resistive index and postoperative outcome in major high risk surgery


Description:

Renal resistive index was measured just after major high risk operations and then patients were observed searching for any surgical and medical-related complications during the first post-operative week


Recruitment information / eligibility

Status Completed
Enrollment 218
Est. completion date July 2013
Est. primary completion date June 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- age > 18 years

- major surgical operations

Exclusion Criteria:

- age < 18 years

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
Italy Sant'Ambrogio Clinical Institute - Cardiac Anesthesia Unit Milano
Italy Humanitas Research Hospital - Dept. Anesthesia and Intensive Care Unit Rozzano Milano

Sponsors (1)

Lead Sponsor Collaborator
Istituto Clinico Humanitas

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Complications Recording any postoperative complication occurred within the first postoperative week 7 post-operative days Yes
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