Hip Fracture in Cauca. Cohort Study
-
- STATUS
- Recruiting
-
- participants needed
- 80
-
- sponsor
- Universidad del Cauca
Summary
This research project is an observational, analytical, prospective cohort study, which aims
to identify and describe the causes of delay in surgical intervention in patients with a
diagnosis of
In order to carry out this investigation, the recruitment of patients over 18 years old, who
enter our institution with a diagnosis of
It is clear that this study does not represent any risk for the participants, the information collected will be confidential and will not be used for any other purpose outside the investigation.
Description
At present there is no consensus on the intervention time of these
The general objective of this study is to identify the main causes of delay in surgical
intervention in patients with a diagnosis of
The research team has also proposed the following specific objectives to carry out this
- study
-
- Describe socio-demographically the patients with a diagnosis of
hip fracture , underwentsurgery at the San Jos University hospital since 2019. - Identify the reason that delay in surgical intervention.
- Quantify the main outcomes in morbidity and mortality during the 6 months after
surgery , associated with the delay insurgery in the study population. - Assess the quality of post-surgical life in the patient operated on for
hip fracture . - Correlate the delay in surgical intervention with complications and mortality in
patients operated for
hip fracture since 2019.
- Describe socio-demographically the patients with a diagnosis of
It is estimated to include 80 patients during the first year of recruitment. For the collection of information there is a sociodemographic survey, the EQ5D5L quality of life survey and comorbidity is evaluated taking into account the Charlson index.
Details
Condition |
|
---|---|
Age | 18years - 100years |
Treatment | Osteosynthesis |
Clinical Study Identifier | NCT04217642 |
Sponsor | Universidad del Cauca |
Last Modified on | 19 February 2024 |
How to participate?
,
Select a site
Enter your location to find study centers near you
study centers available
Send a message
Enter your contact details to connect with study team
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
Learn moreSimilar trials to consider
Browse trials for
Not finding what you're looking for?
Sign up as a volunteer to stay informed
Every year hundreds of thousands of volunteers step forward to participate in research. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.
Sign up as volunteerStudy AnnotationsStudy Notes
Enable the functional cookies in order to view/reply the sharedadd your annotations.
Add a private note
- Select a piece of text from the left.
- Add notes visible only to you.
- Send it to people through a passcode protected link.
Publish Annotation
Are you sure you want to publish the annotation?
Delete AnnotationNote
Are you sure you want to delete the annotationnote?
Study Definition
WikipediaAdd a private note
- Select a piece of text.
- Add notes visible only to you.
- Send it to people through a passcode protected link.