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NCT02198820 Clinical Trial

Practice Survey on Femoral Neck Fractures and the Incidence of Type of Anesthesia on Patient Outcome

Femoral Neck Fractures Clinical Trial

Official title:
Practice Survey on Femoral Neck Fractures and the Incidence of Type of Anesthesia on Patient Outcome in the Saint-Luc Bouge Hospital

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT02198820
Other study ID # FNF-SLBO
Secondary ID
Status Withdrawn
Phase N/A
First received July 23, 2014
Last updated June 22, 2015
Start date October 2014
Est. completion date September 2015

Study information
Verified date June 2015
Source Astes
Contact n/a
Is FDA regulated No
Health authority Belgium: Ethics Committee
Study type Observational [Patient Registry]

Clinical Trial Summary

Inclusion of all patients with femoral neck fracture presenting in Saint-Luc Bouge Hospital between October 1th 2014 and September 30th 2015.

Comparison of severity scores of these patients and the scale of Nottingham on immediate (day 1 and day 2) and late (1 month) outcome.

Description:

Inclusion of all patients with femoral neck fracture presenting in Saint-Luc Bouge Hospital between October 1th 2014 and September 30th 2015.

Comparison of severity scores of these patients and the scale of Nottingham on immediate (day 1 and day 2) and late (1 month) outcome.

This comparison includes preoperative parameters (hemoglobin, creatinine, mini-mental test) and intraoperative parameters (such as type of anesthesia).

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date September 2015
Est. primary completion date September 2015
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- All patients admitted at the Saint-Luc Bouge Hospital for a femoral neck fractures between 10/01/2014 and 30/09/2014

Exclusion Criteria:

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Drug:
• General Anesthesia
General anesthesia with proposal, rocuronium and sufentanil
• Loco Regional Anesthesia
Loco Regional Anesthesia with marcaine

Locations
Country Name City State
Belgium Clinique Saint-Luc de Bouge Namur

Sponsors (1)
Lead Sponsor Collaborator
Astes

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary Preoperative assessment Comparison of the impact of preoperative parameters (such as hemoglobin, creatinine, mini-mental test) on patient outcome. 1 month No
Secondary Perioperative assessment Comparison of the impact of the type of anesthesia (general versus loco regional) on patient outcome. 1 month Yes
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