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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03205384
Other study ID # CHN
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 2017
Est. completion date June 2019

Study information

Verified date March 2020
Source Hospital of Navarra
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Morbimortality in older patients undergoing abdominal surgery.


Description:

The aim of this study is to validate the modified CriSTAL tool for 30 mortality in elderly patients undergoing urgent abdominal surgery. To provide a new tool that could be used in conjunction with clinical judgment to aid in decision-making.

The second objective of our study was to assess the quality of life, frailty, functional status and nutritional status in elderly patients that survive six months after an urgent abdominal surgery.


Recruitment information / eligibility

Status Completed
Enrollment 500
Est. completion date June 2019
Est. primary completion date June 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 65 Years to 110 Years
Eligibility Inclusion Criteria:

- >65 years old, accepted in emergency department

Exclusion Criteria:

- not sign the consent

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
surgery


Locations

Country Name City State
Spain UPNA Pamplona Navarra

Sponsors (1)

Lead Sponsor Collaborator
Hospital of Navarra

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Other FRAIL scale, Fried score To measure frailty 6 months
Primary Barthel index, questionnaire to measure performance in activities of daily living 6 months
Secondary Clavien- Dindo Modified Morbimortality using Clavien-Dindo classification 1 year
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