Morbid Obesity: Effects of Conservative Treatments and Gastric Bypass Surgery
NCT ID: NCT00239850
Last Updated: 2017-03-24
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.
COMPLETED
NA
209 participants
INTERVENTIONAL
2005-08-31
2007-08-31
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.
Surgical Treatment for Morbid Obesity by Sleeve Gastrectomy Versus Gastric Bypass
NCT00722995
Suboptimal Weight Loss After Gastric Bypass Surgery
NCT01829906
Quality of Life Following Gastric Bypass Surgery.
NCT02032199
Guidance in Diet and Physical Activity for Prevention of Weight Gain After Gastric Bypass Surgery
NCT01270451
Lifestyle vs.Surgery for Morbid Obesity Treatment
NCT02122029
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.
NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
lifestyle changes
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Psychologically unstable
* Unable to participate in the training program
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
St. Olavs Hospital
OTHER
Norwegian University of Science and Technology
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.
Baard Kulseng, PhD, MD
Role: PRINCIPAL_INVESTIGATOR
St. Olavs Hospital, Trondheim
Ronald Mårvik, PhD, MD
Role: PRINCIPAL_INVESTIGATOR
St. Olavs Hospital, Trondheim
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
St. Olavs Hospital
Trondheim, , Norway
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Martins C, Strommen M, Stavne OA, Nossum R, Marvik R, Kulseng B. Bariatric surgery versus lifestyle interventions for morbid obesity--changes in body weight, risk factors and comorbidities at 1 year. Obes Surg. 2011 Jul;21(7):841-9. doi: 10.1007/s11695-010-0131-1.
Ovrebo B, Strommen M, Kulseng B, Martins C. Bariatric surgery versus lifestyle interventions for severe obesity: 5-year changes in body weight, risk factors and comorbidities. Clin Obes. 2017 Jun;7(3):183-190. doi: 10.1111/cob.12190. Epub 2017 Mar 20.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
NSD12820
Identifier Type: OTHER
Identifier Source: secondary_id
05/3344TSP
Identifier Type: OTHER
Identifier Source: secondary_id
4.2005.33
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.