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
4 participants
INTERVENTIONAL
2021-06-01
2022-08-26
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.
Endoscopic Gastric Mucosal Ablation as a Primary Obesity Therapy
NCT05486338
Influence of Central Obesity on the Esophageal Epithelial Barrier
NCT02776982
Eon™ FR 1064 Full Abdomen Clinical Study Protocol
NCT04842110
Contributing Factors in the Pathobiology of Airway Remodeling in Obesity
NCT03115632
Endoscopic Sleeve Gastroplasty (ESG) for the Treatment of Obesity
NCT06339320
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.
NA
SINGLE_GROUP
OTHER
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Subjects with Obesity
Subjects will be recruited to undergo endoscopic sleeve gastroplasty. The subjects will be studied at baseline, 30, 60, 90 days after procedure
endoscopy sleeve gastroplasty
endoscopic procedure for weight loss
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
endoscopy sleeve gastroplasty
endoscopic procedure for weight loss
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Evidence of insulin resistance as defined by hemoglobin A1c \> 5.7%.
* Mayo Clinic patients evaluated by Dr. Rahul Pannala.
* Pursue an endoscopic gastroplasty at Mayo Clinic Arizona in the Gastroenterology department.
* Equal distribution of gender.
* 18 yo older of age.
* BMI\>30 kg/m2.
* Nonsmoker.
* Taking no medication affecting glucose or lipid metabolism.
* No more than 5% change in body weight in the previous 6 months.
* Mostly sedentary (engaging in strenuous exercise (\> 70% max HR) less than 3 times a week).
* Not be receiving corticosteroid therapy.
* Have no history of asthma, COPD or atopic syndrome, or autoimmune disease (Ulcerative colitis, Chron's disease, eosinophilic esophagitis, any rheumatologic disease such as lupus, rheumatoid arthritis, Sjogren syndrome).
Exclusion Criteria
* BMI \<30 kg/m2.
* Smoker.
* Taking medication affecting glucose or lipid metabolism.
* Greater than 5% change in body weight within the previous six months.
* Engage in strenuous exercise (\>70% max HR) less than 3 times a week.
* Receiving corticosteroid therapy.
* Have a history of asthma.
* History of COPD or atopic syndrome.
* History of autoimmune disease (Ulcerative colitis, Chron's disease, eosinophilic esophagitis, any rheumatologic disease such as lupus, rheumatoid arthritis, Sjogren syndrome).
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Mayo Clinic
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Elena Anna (Eleanna) De Filippis, M.D., Ph.D.
Principal Investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Elena Anna O. De Filippis, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Mayo Clinic
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Mayo Clinic in Arizona
Scottsdale, Arizona, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
21-000959
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.