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STOX1 as a Predictor of Bariatric Surgery Efficacy and Obesity Correlation Study

STOX1 as a Predictor of Bariatric Surgery Efficacy and Obesity Correlation Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400093677
Enrollment
Unknown
Registered
2024-12-10
Start date
2025-01-01
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

Obesity and insulin resistance

Interventions

Sponsors

Chongqing Dazu District People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1.100 cases of type 2 diabetes group: patients with type 2 diabetes mellitus whose blood glucose is not controlled by diet and exercise. Type 2 diabetes mellitus was diagnosed according to the 1999 WHO criteria; 2.100 cases of simple obesity group: BMI >= 28kg/m^2; 3. equal number of normal control group. All subjects need to meet the age of 18-75 years old, male or female; no serious diseases of various systems; able to understand and willing to strictly comply with the clinical trial protocol to complete the trial, and voluntarily sign the informed consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria (fulfilment of one of the following precludes enrolment): 1. the patient is allergic to the drugs involved in the study; 2. use of any of the following drugs or treatments prior to randomisation: 1) Growth hormone within 6 months; 2) History of substance abuse within 6 months; 3) Use of any glucose-lowering medication within 2 months; 4) Participation in a clinical trial of any drug or medical device within 2 months; 5) Use of more than 7 days of corticosteroid therapy within 2 months; 6) Use of medication with weight control effects (e.g., sibutramine, rimonabant, orlistat) or any procedure that can cause weight change within 2 months; 7) Use of any kind of medication that could have an impact on the safety of the treatment and the accuracy of the data.

Design outcomes

Primary

MeasureTime frame
Obeisty;Insulin resistance;

Secondary

MeasureTime frame
Inflammatory factors;

Countries

China

Contacts

Public ContactYanping Wang

Chongqing Dazu District People's Hospital

839349881@qq.com+86 130 3667 2995

Outcome results

None listed

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