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A pilot study of the medroxyprogesterone + metformin combination therapy for the endometrial cancer

A pilot study of the medroxyprogesterone + metformin combination therapy for the endometrial cancer - A pilot study of the medroxyprogesterone + metformin combination therapy for the endometrial cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000002210
Enrollment
40
Registered
2009-07-16
Start date
2009-02-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

endometrial cancer atypical endometrial hyperplasia

Interventions

Patients were scheduled to received 400mg per day of medroxyprogesterone acetate with 100mg of aspirin orally on a daily basis for 24weeks. The metformin combines concurrently. We administer the m

Sponsors

chiba university
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) Histrogically confirmed well differentiated endometrioid adenocarcinoma at presumed stage IA and atypical endometrial hyperplasia (2) myometrium invasion was ruled out by MRI (3)performance status of 0 to 1 (4) serum creatinine <1.0mg/dl (5) A case without hypersensitivity for this treatment use medicine (6) The case that written informed consent was obtained before participation

Exclusion criteria

Exclusion criteria: (1) The case with a history of the hypersensitivity that is serious for this study use medicine or the drug allergy (2)A history of the lactic acidosis (3)Patients on dialysis (4)Shock, failure heart, myocardial infarction, a cardiovascular injury including the pulmonary embolism (5)Excessive alcohol intake (6)Hepatic dysfunction (7) A history of the thrombosis (8)A case with the psychic disturbance that it seems that we need in the treatment or treatment with antimental medicine (9) Patients with diabetes (10)A case with the double cancer of the activity (11)In addition, the case that the chief physician judged to be inadequate.

Design outcomes

Primary

MeasureTime frame
Recurrence free interval

Secondary

MeasureTime frame
Primary complete response rate Pregnancy rate Side effect

Countries

Japan

Contacts

Public ContactAkira Mitsuhashi

Graduate School of Medicine, Chiba University Reproductive medicine

antira@faculty.chbia-u.jp043-222-7171

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026