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Apoptotic Signaling Pathways in Rats With Endometrial Hyperplasia

The Effect of Metformin and Medroxyprogesterone Acetate on Apoptotic Signaling Pathways in Wistar-Albino Rats With Induced Endometrial Hyperplasia

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02872818
Enrollment
40
Registered
2016-08-19
Start date
2014-10-31
Completion date
2015-03-31
Last updated
2016-08-23

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

Conditions

Apoptotic Signal Pathways in Endometrial Hyperplasia

Keywords

Apoptotic signal pathway, Survivin, Bcl-2, Bax, c-Myc, Caspase-9, endometrial hyperplasia, endometrium cancer

Brief summary

The purpose of the study is to determine apoptotic signaling pathways such as Survivin, Bcl-2, Bax, c-Myc and caspase-9 expression levels in rats model with iatrogenic endometrial hyperplasia after metformin and medroxyprogesterone acetate administration.

Interventions

DRUG17β estradiol hemihydrate

4mg/kg/day for 20 days

DRUGMetformin

50 mg/kg/day last 10 days

DRUGmedroxyprogesterone acetate

1mg/kg/day last 10 days

Sponsors

Kayseri Education and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
8 Weeks to 10 Weeks
Healthy volunteers
No

Inclusion criteria

Forty-eight weeks old female Wistar-Albino rats, weighting between 180 and 260 g

Exclusion criteria

. We have no

Design outcomes

Primary

MeasureTime frame
Survivin Gene Expression Levels in Rat Uterine Tissue4 months
Bcl-2 Gene Expression Levels in Rat Uterine Tissue4 months
Bax Gene Expression Levels in Rat Uterine Tissue4 months
c-Myc Gene Expression Levels in Rat Uterine Tissue4 months
Caspase-9 Expression Levels in Rat Uterine Tissue4 months

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026