Effect of Bariatric Surgery on Cognition, Genetics and Lifestyle
NCT ID: NCT02085369
Last Updated: 2021-03-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
100 participants
OBSERVATIONAL
2014-01-31
2023-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Cognitive Impairment, Obesity, and the Effects of Bariatric Surgery
NCT05215886
Change in Cognitive Function in Obese Patients After Bariatric Surgery - an Observational Study
NCT01554228
Prevalence of Complications After Bariatric Surgery - an Epidemiologic Survey
NCT01930929
Prevention of Coronary Heart Disease in Morbidly Obese Patients
NCT00626964
Quality of Life Following Gastric Bypass Surgery.
NCT02032199
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Uppsala University Hospital
OTHER
Uppsala University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Magnus Sundbom, MD
Role: PRINCIPAL_INVESTIGATOR
Academic Hospital Uppsala
Helgi Schiöth, Prof
Role: STUDY_DIRECTOR
Uppsala University
Olga Titova, PhD
Role: STUDY_DIRECTOR
Uppsala University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Uppsala University Hospital
Uppsala, , Sweden
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
PH2014
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
PH2014
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.