- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03265275
Why Still in Hospital After Hip Fracture Surgery?
November 26, 2020 updated by: Asbjorn Aroen, University Hospital, Akershus
At our institution, hip fracture patients are admitted and treated according to a fast track patient pathway.
The aim of this study is to identify areas of this patient pathway that can be improved.
To achieve this, the study will investigate the underlying reasons for the continued need for hospitalization on the consecutive days after hip fracture surgery.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The study will be conducted at the orthopedic department, Akershus University Hospital, as a prospective observational study and will include approximately 200 consecutive hip fracture patients.
The patients will be evaluated once daily for the fulfillment of predefined discharge criteria.
If the discharge criteria are not met or if the criteria are met but the patient is not discharged in spite of this the underlying reason(s) are recorded.
Study Type
Observational
Enrollment (Actual)
182
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Lørenskog, Norway, 1478
- Akershus University Hospital
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients over 18 years of age, who have been operated for a hip fracture at the orthopedic department, Akershus University Hospital.
Description
Inclusion Criteria:
- Operated at the orthopedic department, Akershus University Hospital, for a hip fracture
Exclusion Criteria:
- Lack of written informed consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Factors necessitating hospitalization after hip fracture surgery
Time Frame: Recorded using a check-list once daily from first day after hip fracture surgery until discharge from the orthopedic department, typically between 1 to 14 days after hip fracture surgery
|
Recorded as: acute anemia, delirium, medical complications, pain, dizziness, nausea/vomiting, logistical reasons, unwillingness to be discharged, other (specified as free text)
|
Recorded using a check-list once daily from first day after hip fracture surgery until discharge from the orthopedic department, typically between 1 to 14 days after hip fracture surgery
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of patients discharged to their preoperative level of care
Time Frame: At hospital discharge, typically between 1 to 14 days after hip fracture surgery
|
At hospital discharge, typically between 1 to 14 days after hip fracture surgery
|
|
|
Length of hospital stay
Time Frame: At hospital discharge, typically between 1 to 14 days after hip fracture surgery
|
Length of hospital stay in days, stratified after type of operation
|
At hospital discharge, typically between 1 to 14 days after hip fracture surgery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
September 11, 2017
Primary Completion (ACTUAL)
February 28, 2020
Study Completion (ACTUAL)
March 31, 2020
Study Registration Dates
First Submitted
August 23, 2017
First Submitted That Met QC Criteria
August 25, 2017
First Posted (ACTUAL)
August 29, 2017
Study Record Updates
Last Update Posted (ACTUAL)
November 30, 2020
Last Update Submitted That Met QC Criteria
November 26, 2020
Last Verified
November 1, 2020
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2017/CP
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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