- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02817295
Bariatric Surgeries in Elderly
February 5, 2017 updated by: Sergio Gabriel Susmallian, Assuta Medical Center
an examination of the different aspects of bariatric surgery in elderly in comparison with non-elderly patients.
Study Overview
Detailed Description
the study examines the success rate, complications, revisions, days of hospitalization and co-morbidities in elderly and in non-elderly patients that underwent bariatric surgery in our medical center
Study Type
Observational
Enrollment (Actual)
9000
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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Tel-Aviv, Israel
- Assuta Medical Center
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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 to 85 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
patients underwent baritaric surgery
Description
Inclusion Criteria:
bariatric surgery
Exclusion Criteria:
below 18 years old
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 |
---|---|
elderly
patients underwent bariatric surgery and are above 65 years old
|
follow up on the number of complications, revisions, hospitalization and co-morbidities
|
non-elderly
patients underwent bariatric surgery and are below 65 years old
|
follow up on the number of complications, revisions, hospitalization and co-morbidities
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of complications.
Time Frame: six months
|
data collection and analysis will be ended in six months.
data will be collected from the medical records.
|
six months
|
Number of revisions
Time Frame: six months
|
data collection and analysis will be ended in six months.
data will be collected from the medical records.
|
six months
|
Number of days of hospitalization
Time Frame: six months
|
data collection and analysis will be ended in six months.
data will be collected from the medical records.
|
six months
|
Incidence of co-morbidities
Time Frame: six months
|
data collection and analysis will be ended in six months.
data will be collected from the medical records.
|
six months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
January 1, 2016
Primary Completion (Actual)
February 1, 2017
Study Completion (Actual)
February 1, 2017
Study Registration Dates
First Submitted
June 22, 2016
First Submitted That Met QC Criteria
June 26, 2016
First Posted (Estimate)
June 29, 2016
Study Record Updates
Last Update Posted (Estimate)
February 7, 2017
Last Update Submitted That Met QC Criteria
February 5, 2017
Last Verified
February 1, 2017
More Information
Terms related to this study
Other Study ID Numbers
- 2015073
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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