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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04140370
Other study ID # FRAGILE
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date April 15, 2020
Est. completion date December 15, 2020

Study information

Verified date October 2019
Source Hospital Clinic of Barcelona
Contact Carlos Ferrando, MD
Phone +34 932275400
Email cmferrando@clinic.cat
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

European prospective one day cohort study. Analysis of the prevalence of frailty and predefined 30-day postoperative complications in adult patients undergoing emergency or elective surgery.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 6500
Est. completion date December 15, 2020
Est. primary completion date August 15, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients over the age of 18 who will undergo emergency or elective surgery with an intended hospital stay of more than 24 hours and any type of anesthesia.

Exclusion Criteria:

- Outpatient (ie. day case) surgery, obstetric analgesia or anesthesia, organ transplant surgery, cardiac surgery, neurosurgery.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
There is no intervention
There is no intervention

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
Hospital Clinic of Barcelona Spanish Multimodal Rehabilitation Group, Spanish Sociey of Anesthesiology

Outcome

Type Measure Description Time frame Safety issue
Primary The percentage of patients with frailty identified in the preoperative assessment in both elective and emergency surgery, as well as frailty's severity. 30 days
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