Skip to content

A Multicenter, Randomized, Parallel-controlled Clinical Study of the Effect of Orlistat Combined with Pyretone and Metformin on Blood Glucose in Type 2 Diabetes Mellitus Patients with Obesity

A Multicenter, Randomized, Parallel-controlled Clinical Study of the Effect of Orlistat Combined with Pyretone and Metformin on Blood Glucose in Type 2 Diabetes Mellitus Patients with Obesity

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059191
Enrollment
Unknown
Registered
2022-04-26
Start date
2022-08-01
Completion date
Unknown
Last updated
2024-02-19

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

Conditions

Type 2 diabetes mellitus

Interventions

control group:Pioglitazone metformin + orlistat a placebo
experimental group:Pioglitazone and metformin tablets + orlistat capsules

Sponsors

Shanghai Tenth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Diagnostic criteria for diabetes in patients with type 2 diabetes; 2. Fasting blood glucose =28.0 kg/m^2; 5. Female patients did not plan to have children during the study and took corresponding contraceptive measures (excluding contraceptive pills); 6. C peptide index > 0.3ng/ml.

Exclusion criteria

Exclusion criteria: 1. Abnormal liver function, ALT, AST is more than 2.5 times the upper limit of normal; 2. Renal function impairment, serum creatinine: female >=133µmol/L, male >=135µmol/L; eGFR grading >=60ml/min/1.73m^2; 3. Patients with severe chronic gastrointestinal diseases: chronic malabsorption syndrome or cholestasis; Having undergone enterectomy or other abdominal surgery; Active stage of digestive tract ulcer; 4. Patients with severe heart, lung, liver and kidney diseases and tumor history; 5. Patients with mental disorders, drug or other substance abuse; 6. Allergic to orlistat, metformin, pioglitazone or any of the ingredients or frequent hypoglycemia; 7. History of brittle fractures caused by osteoporosis and non-violent fractures within the past 6 months; 8. Pregnant or lactating patients; 9. Patients considered unsuitable for this study by the investigators.

Design outcomes

Primary

MeasureTime frame
HbA1C;height;weight;waist;hip circumference;oral glucose tolerance test;fasting blood-glucose;insulin;blood fat;

Countries

China

Contacts

Public ContactQu Shen
qushencn@hotmail.com+86 21 66301604

Outcome results

None listed

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