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Effect of Pioglitazone in Breast Cancer

Comparative Analysis of Radiologic Response of Pioglitazone with Chemotherapy versus Chemotherapy with Placebo in Metastatic Breast Cancer.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180124038493N1
Enrollment
62
Registered
2018-09-10
Start date
2017-10-23
Completion date
Unknown
Last updated
2018-10-11

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

Conditions

Breast Cancer. Malignant neoplasm of breast

Interventions

Intervention 1: Intervention group: Pioglitazone tablet of thiazolidinedione class osveh pharmacy prescribe one tablet daily with each meal for 6 monthes.Add to routine chemotherapy drugs based on Tax

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Women With Confirmed Pathologic Invasive Breast Cancer Represented by Mesaurable Visceral Metastases These Women should Aged at least 18 years old Performance Status(ECOG) should be 0-2 life Expectancy should be more than 3 months

Exclusion criteria

Exclusion criteria: Usage this group of drug during 12 months ago. Class III/IV Heart failure of New YORK HEART ASSOCIATION Hiv Positive, Pregnant or Breast Feading, Previous History or Active Bladder cancer NCI TOXICITY CRITERIA Grade 3,4 (VER 2.0) Total Billirubin more than 1.5 times upper limit Normal or liver enzymes more than 2.5 times upper limit Normal unless liver Metastasis make this limitation change to 5. Osteoporetic Patients (who = Tscore -2.5SD)

Design outcomes

Primary

MeasureTime frame
Treatment Radiologic Responses ( stable/partial/ complete/progressive). Timepoint: Before Intervention, Month 3, Month 6. Method of measurement: Recist criteria version 1.1.;Lesion Size. Timepoint: Before Intervention, Month 3, Month 6. Method of measurement: Ruler in ct scan software.

Secondary

MeasureTime frame
Time to progression. Timepoint: Month 3 and 6 from start study. Method of measurement: Watching.;Survival. Timepoint: Month 3 and 6 from start study. Method of measurement: watching.;Response Rate (percentage of patients whose cancer shrinks or disappears after treatment). Timepoint: Month 3 and 6 from start study. Method of measurement: Radiographic Response.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Moghareabed

Esfahan University of Medical Sciences

Rezamoghareabed@yahoo.com+98 31 3620 6006

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 20, 2026