ClinicalTrials.gov
 Home    Search    Study Topics    Glossary  
 

  Full Text View  
  Tabular View  
  Contacts and Locations  
  No Study Results Posted  
  Related Studies  
Estrogen Modulation of Mood and Cognition Following Monoaminergic Depletion in Post-Menopausal Women

This study is currently recruiting participants.
Verified by National Center for Research Resources (NCRR), December 2003

Sponsored by: National Center for Research Resources (NCRR)
Information provided by: National Center for Research Resources (NCRR)
ClinicalTrials.gov Identifier: NCT00005768
  Purpose

This study will examine whether estrogen administration in postmenopausal women can alter the response to changes in brain chemistry brought about by dietary manipulation. Women who are recently menopausal (50-60 yrs. of age) and over 20 years postmenopausal (>70 yrs. of age) will take estrogen or placebo for three months. At the end of that time they will participate in three challenges using dietary techniques to briefly change the relative amounts of neurotransmitters in the brain that are believed to be related to mood regulation (serotonin, dopamine, and norepinephrine). Previous research has shown that these dietary manipulations can briefly produce negative changes in mood. The investigator hypothesizes that estrogen administration will blunt or buffer these negative effects in a quantifiable way. The investigator believes that this will provide a direct test of the ability of estrogen to meaningfully change the brain chemistry of mood in a clinically measurable and positive way. The proposed procedure will also allow assessment of the effects of estrogen on brain neurotransmitter systems after many years of very low estrogen levels.


Condition Intervention Phase
Menopause
Drug: Estrogen
Phase II

MedlinePlus related topics:   Menopause   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Double-Blind
  Eligibility
Ages Eligible for Study:   50 Years and older
Genders Eligible for Study:   Female
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Postmenopausal
  • Non-smoker
  • BMI <30
  • Healthy
  • Without surgically-induced menopause
  • Not on HRT or >1 year post HRT
  • Normal mammogram within last year
  • No cardiovascular disease other than mild hypertension
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00005768

Contacts
Contact: Julie Dumas     1-802-847-2523    

Locations
United States, Vermont
University of Vermont     Recruiting
      Burlington, Vermont, United States, 05401
      Contact: Julie Dumas     802-847-2523        
      Principal Investigator: Paul Newhouse, M.D.            

Sponsors and Collaborators
  More Information


Study ID Numbers:   NCRR-M01RR00109-0741, M01RR00109
First Received:   June 1, 2000
Last Updated:   June 23, 2005
ClinicalTrials.gov Identifier:   NCT00005768
Health Authority:   United States: Federal Government

Study placed in the following topic categories:
Menopause

ClinicalTrials.gov processed this record on December 03, 2008




Links to all studies - primarily for crawlers