Clinical Trials Directory

Trials / Unknown

UnknownNCT00005769

Hormone Replacement Therapy and Insulin Action: A Double-Blind, Parallel, Placebo-Controlled Hormone Intervention Study in Postmenopausal Women

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
Sponsor
National Center for Research Resources (NCRR) · NIH
Sex
Female
Age
45 Years – 55 Years
Healthy volunteers
Not accepted

Summary

Considerable controversy exists regarding the effect of estrogen and progesterone on insulin sensitivity in postmenopausal women. Thus, the goal is to examine the effect of estradiol and progestin on in vivo insulin sensitivity and pathways of intracellular glucose metabolism in postmenopausal women. This will be accomplished by examining the effects of unopposed estrogen (CEE) or combination estrogen and progestin (CEE/MPA) versus placebo therapy in 30 early menopausal women (defined from 6 months to 3 years post-cessation of menses). Women will be treated for 16 weeks and the outcome measures will be: 1) insulin sensitivity and glucose oxidation as determined by euglycemic clamp, 2) assessments of insulin sensitivity on muscle biopsy cultures with the primary endpoints being glucose uptake and glycogen accumulation/synthesis, 3) protein levels of insulin action cascade steps based on muscle biopsy Western blots.

Conditions

Interventions

TypeNameDescription
DRUGHormone Replacement Therapy

Timeline

First posted
2000-06-02
Last updated
2005-06-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00005769. Inclusion in this directory is not an endorsement.