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Research of correlation of central inflammation, peripheral inflammation, and vascular endothelial damage in obese patients

Research of correlation of central inflammation, peripheral inflammation, and vascular endothelial damage in obese patients

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400085587
Enrollment
Unknown
Registered
2024-06-13
Start date
2024-06-15
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Obesity

Interventions

Sponsors

Huashan Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for obese patients: 1) Age 18-60 years (2) Body mass index (BMI) =30kg/m2 (3) Proposed laparoscopic sleeve gastrectomy 4) Patients agreed and signed an informed consent form Inclusion criteria for normal weight study participants: 1) Age 18-60 years old (2) BMI between 18.5 and 24.9 kg/m2. 3) Agreed and signed an informed consent form

Exclusion criteria

Exclusion criteria: Exclusion criteria for obese patients: 1) Patients with severe cardiovascular disease or unstable angina pectoris 2) History of psychiatric disorders, especially those affecting appetite and weight, such as depression, bipolar disorder 3) Use of medications that may significantly affect body weight or metabolism, such as antidepressants, steroids, or antipsychotics. 4) Presence of endocrine disorders known to directly affect body weight and metabolism, e.g., hyper- or hyperthyroidism, Cushing's disease 5) History of neurological disease or significant brain injury 6) Participants who refuse to participate in a clinical trial, sign an informed consent form, or participate in another study at the same time. Exclusion criteria for normal weight study participants: 1) Presence of any chronic disease that may affect body weight or neurological function, such as cardiovascular disease, diabetes, mental illness, blood system diseases, etc. 2) Have abnormal liver function 3) Use of medication that affects body weight, metabolism, or neurological function. 4) Have a history of major neurological disease or brain injury. 5) Recent significant weight changes or extreme dietary behaviours 6) Participants who refuse to participate in the clinical trial, refuse to sign the informed consent form, or participate in other studies at the same time.

Design outcomes

Primary

MeasureTime frame
Heparan Sulfate;

Secondary

MeasureTime frame
Ferritin;C-reactive protein,CRP;Interleukin;NAR;NLR;PNR;PLR;PWR;Cranial diffusion tensor imaging;Central inflammatory markers;

Countries

China

Contacts

Public ContactYu Qiong

Huashan Hospital, Fudan University

yu_qiong816@sina.com+86 134 7275 5168

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026