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Clinical study on the anti-cancer effect of metformin in the breast cancer patients with prediabetes during neoadjuvant chemotherapy.

Clinical study on the anti-cancer effect of metformin in the breast cancer patients with prediabetes during neoadjuvant chemotherapy.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-16008553
Enrollment
Unknown
Registered
2016-05-28
Start date
2016-06-30
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

breast cancer

Interventions

Group 2:metformin,850mg,Bid.

Sponsors

Department of Endocrine and Breast Surgery of the First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Volunteered for this study and informed consent was abtained from the participants; 2. Female and age from 20 to 70 years old; 3. Diagnosis as breast cancer according to clinical practice guideline; 4. Indications for neoadjuvant chemotherapy according to clinical practice guideline: clinical I/II stage breast cancer; 5. Diagnosis as prediabetes: OGTT examinations show IFG 5.6-6.9mmol/L, IGT 7.8-11.0mmol/L; Or HbA1c:5.7-6.4%.

Exclusion criteria

Exclusion criteria: 1. History of diabetes; 2. History of hypoglycemic agent use; 3. Pregnant or breast feeding women; 4. BMI=35kg/m2; 5. Liver and renal function abnormal obviously(ALT greater than 2.5 times of upper bound, or eGFR180mmHg or diastolic pressure>110mmHg); 7. Coexistence of serious heart diseasecardiac function II or aboveanemia(Hb<9.0g/dl); 8. Alcoholismdrug abuse and mental disorder; 9. Coexistence of digestion and absorption dysfunction and other endocrine diseases; 10. Coexistence of other chronic disease and need to treat with glucocorticoid; 11. Coexistence of other serious medical conditions, such as serious infections, organs failure, serious injury, etc.

Design outcomes

Primary

MeasureTime frame
Pathologic complete response(PCR);

Secondary

MeasureTime frame
breast cancer events;Clinical recession of lump;Glucose intolerance and insulin function status;Metabolic syndrome;

Countries

China

Contacts

Public ContactRen Guo-sheng

Department of Endocrine and Breast Surgery of the First Affiliated Hospital of Chongqing Medical University

rgs726@163.com+86 13508370536

Outcome results

None listed

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