- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02820922
Anesthesia for Emergency Orthopedic Surgery
June 28, 2016 updated by: Havva Sayhan, Sakarya University
Anesthetic Techniques for Emergency Orthopedic Surgery
The aim of this retrospective study is to evaluate the preferred anaesthesia techniques in our clinic for emergency orthopedic surgery at a 1 year period.
Study Overview
Detailed Description
This retrospective study included patients of all ages who have undergone emergency orthopedic surgery between January 2015 and December 2015 after approval of the research ethics committee.
Medical record forms and electronic medical record system of the hospital were used in the analysis of medical data with regard to age, sex, ASA score, anaesthesia technique, comorbidities, surgery diagnosis, length of surgery, complications and admission to intensive care unit after surgery.
Study Type
Observational
Enrollment (Anticipated)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Havva Sayhan, assist prof
- Phone Number: +905056621021
- Email: hsayhan@gmail.com
Study Locations
-
-
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Sakarya, Turkey, 54100
- Recruiting
- Sakarya University Research and Training hospital
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Contact:
- Havva Sayhan, assist prof
- Phone Number: +905056621021
- Email: hsayhan@gmail.com
-
Contact:
- Ali F Erdem, prof
- Phone Number: +90 264 8884051
- Email: alifuaterdem@gmail.com
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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
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients of all age groups who administered for orthopedic emergency surgery
Description
Inclusion Criteria:
- all patients who had orthopedic emergency surgery
Exclusion Criteria:
- involvement of incomplete data collection
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Orthopedic emergency surgery
Patients of all ages who have undergone emergency orthopedic surgery The analysis of medical data with regard to age, sex, the American Society of Anesthesiologists (ASA) score, anaesthesia technique, comorbidities, surgery diagnosis, length of surgery, complications and admission to intensive care unit after surgery
|
anesthesia techniques with regard to age, sex, ASA score, anaesthesia technique, comorbidities, surgery diagnosis, length of surgery, complications and admission to intensive care unit after surgery
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of patients with preferred anesthesia technique for orthopedic emergency surgery assessed by Statistical Package for the Social Sciences (SPSS) v22.0
Time Frame: 1 year
|
Statistical assessment would be carried out with regard to anesthesia technique.
Outcome measures the number of patients with demographic data arrive at orthopedic emergency service.
Results will be helpful on preferred anesthesia technique at orthopedic emergency surgery in our clinic.
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Assessment of ages and anesthesia technique relation on orthopedic emergency surgery by SPSS v22.0
Time Frame: 3 months
|
Age is a factor that make changes relevant to anesthesia.
The study analyze the influence of age on anesthesia technique at orthopedic emergency surgery.
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3 months
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Assessment of orthopedic surgery type and anesthesia relation on orthopedic emergency surgery by SPSS v22.0
Time Frame: 3 months
|
Statistical evaluation of orthopedic surgery type relevant to anesthesia.
The study analyze the influence of surgery type on preferred anesthesia technique at our hospital.
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Ali F Erdem, Prof, Sakarya University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Clark L, Robinson M, Varbanova M. Role of regional anesthesia in orthopedic trauma. Anesthesiol Clin. 2014 Dec;32(4):789-808. doi: 10.1016/j.anclin.2014.08.002. Epub 2014 Nov 25.
- Stundner O, Ortmaier R, Memtsoudis SG. Which outcomes related to regional anesthesia are most important for orthopedic surgery patients? Anesthesiol Clin. 2014 Dec;32(4):809-21. doi: 10.1016/j.anclin.2014.08.003. Epub 2014 Nov 25.
- Campbell VL. Anesthetic protocols for common emergencies. Vet Clin North Am Small Anim Pract. 2005 Mar;35(2):435-53. doi: 10.1016/j.cvsm.2004.10.005.
Helpful Links
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
March 1, 2016
Primary Completion (ANTICIPATED)
February 1, 2017
Study Completion (ANTICIPATED)
June 1, 2017
Study Registration Dates
First Submitted
June 24, 2016
First Submitted That Met QC Criteria
June 28, 2016
First Posted (ESTIMATE)
July 1, 2016
Study Record Updates
Last Update Posted (ESTIMATE)
July 1, 2016
Last Update Submitted That Met QC Criteria
June 28, 2016
Last Verified
June 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Sakarya University
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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