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NCT03497949 Clinical Trial

Peri-operative Vasopressor Support in Patients Operated for an Acute Hip Fracture (AHF)

Hip Fractures Clinical Trial

Official title:
Peri-operative Vasopressor Support in Patients Operated for an Acute Hip Fracture (AHF)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03497949
Other study ID # Hip vasopressor
Secondary ID
Status Completed
Phase
First received April 10, 2018
Last updated April 13, 2018
Start date January 20, 2017
Est. completion date March 31, 2018

Study information
Verified date April 2018
Source Sahlgrenska University Hospital, Sweden
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The incidence of hypotension perioperatively during operation of an acute hip fracture is unknown. As a surrogate factor the usage of vasopressor support is more adequate as the registration of vasopressor drugs are many times not complete in records. The investigators retrospectively investigated the anesthetic journals of 1100 patients with an acute hip fracture (AHF) noting confounding factors and the usage of vasopressors either by injections or infusions and then correlated these results to mortality at 30-, 90- and 365- days

Description:

The incidence of hypotension perioperatively during operation of an acute hip fracture is unknown. As a surrogate factor the usage of vasopressor support is more adequate as the registration of vasopressor drugs are many times not complete in records. The investigators retrospectively investigated the anesthetic journals of 1100 patients with an acute hip fracture (AHF) noting confounding factors and the usage of vasopressors either by injections or infusions and then correlated these results to mortality at 30-, 90- and 365-days Confounding factors were; all comorbitity, age, ASA grade as well as type of anesthesia

Recruitment information / eligibility
Status Completed
Enrollment 997
Est. completion date March 31, 2018
Est. primary completion date March 31, 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria

- Patients with an acute hip fracture

Exclusion Criteria

- Only one fracture within time-limit.

- Unretreivable mortality data

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Sweden SahlgrenskaUH Molndal VGR

Sponsors (1)
Lead Sponsor Collaborator
Sahlgrenska University Hospital, Sweden

Country where clinical trial is conducted

Sweden, 

Outcome
Type Measure Description Time frame Safety issue
Primary Mortality 365 days
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