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A Prospective Real-World Study on the Effects of Sleeve Gastrectomy, Gastric Bypass Stenting, and GLP-1 Receptor Agonists on Brain Function in Patients with Obesity

A Prospective Real-World Study on the Effects of Sleeve Gastrectomy, Gastric Bypass Stenting, and GLP-1 Receptor Agonists on Brain Function in Patients with Obesity

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600132332
Enrollment
Unknown
Registered
2026-09-11
Start date
2026-09-11
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Interventions

Normal-Weight Reference Group:None
Gastric Bypass Stenting Group:None
GLP-1 Receptor Agonist Therapy Group:None

Sponsors

Shanghai Tenth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Age 18–60 years. 2.Body mass index (BMI) = 28 kg/m² for the intervention groups; BMI 18.5–23.9 kg/m² for the normal-weight reference group. 3.Based on clinical evaluation, participants were assigned to one of the following groups: sleeve gastrectomy, gastric bypass stenting, GLP-1 receptor agonist therapy, or a normal-weight reference group, and met the corresponding eligibility criteria for each group. 4.Willingness to participate and provision of written informed consent prior to enrollment.

Exclusion criteria

Exclusion criteria: 1.Age <18 years or =60 years; 2.BMI =28 kg/m² for the intervention groups, or BMI outside the range of 18.5–23.9 kg/m² for the reference group; 3.Failure to meet the inclusion criteria for any of the four study groups. 4.Presence of contraindications to any of the assigned interventions. 5.History of neurological disorders (e.g., stroke, brain tumor, epilepsy) or traumatic brain injury. 6.Contraindications to MRI examination (e.g., metallic implants, cardiac pacemaker, claustrophobia). 7.Severe dysfunction of major organs, including heart, liver, or kidney (e.g., Child–Pugh class C, estimated glomerular filtration rate [eGFR] <30 mL/min/1.73 m², New York Heart Association [NYHA] class IV). 8.Pregnancy or lactation. 9.Severe psychiatric disorders (e.g., schizophrenia, bipolar disorder) or cognitive impairment (Mini-Mental State Examination [MMSE] score <24). 10.Participation in other interventional clinical studies within the past 3 months. 11.Any other conditions deemed by the investigators to render the participant unsuitable for this study.

Design outcomes

Primary

MeasureTime frame
Brain function MRI (fMRI) indicators: changes in brain area activation related to tasks (food craving), changes in resting-state functional connectivity;

Secondary

MeasureTime frame
Cognitive and behavioral assessments;biochemical and multi-omics analyses;tissue analyses;Gastric ultrasonography;psychological scale evaluations;

Countries

China

Contacts

Public ContactBu Le

Shanghai Tenth People's Hospital

geyingjun@hotmail.com+86 21 66303542

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Sep 19, 2026