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Effect of Dehydroepiandrosterone (DHEA) on Hot Flashes in Postmenopausal Women

Primary Purpose

Hot Flashes

Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Placebos
DHEA capsule
Sponsored by
CHU de Quebec-Universite Laval
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hot Flashes focused on measuring Hot Flashes, Menopause, Quality of Life, Hot flushes

Eligibility Criteria

40 Years - 70 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria: Healthy postmenopausal women with 50 or more moderate to severe hot flushes. Women between 40 to 70 years of age. Exclusion Criteria: Body mass index (BMI) of 35 kg/m2 or more. Significant metabolic and endocrine diseases. Diagnosis of cancer. Use of steroids or drugs that interfere with the metabolism of estrogen. Use of any systemic estrogen, progestin, or DHEA in the eight weeks prior to randomization. Use of alternative therapies or natural products to treat postmenopausal symptoms in the four weeks prior to randomization. Palpable fibroids or uterine prolapse: Grade 2 or 3. Cigarette smoking

Sites / Locations

  • Clinique des Traitements Hormonaux

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Placebo

DHEA

Arm Description

Outcomes

Primary Outcome Measures

Use of a diary to monitor the number and intensity of hot flashes as compared to placebo at screening, day 1, weeks 2, 4, 8, 12 and 16

Secondary Outcome Measures

Evaluation of safety as well as quality of life, psychological general well being, and sexual life by questionnaires at day 1, 2, 4, 8, 12 and 16 weeks of treatment

Full Information

First Posted
April 20, 2006
Last Updated
April 6, 2017
Sponsor
CHU de Quebec-Universite Laval
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1. Study Identification

Unique Protocol Identification Number
NCT00317148
Brief Title
Effect of Dehydroepiandrosterone (DHEA) on Hot Flashes in Postmenopausal Women
Official Title
Phase II-III Placebo-Controlled, Study to Evaluate the Effects of DHEA on Vasomotor Symptoms (Hot Flashes) in Postmenopausal Women
Study Type
Interventional

2. Study Status

Record Verification Date
April 2017
Overall Recruitment Status
Completed
Study Start Date
August 2005 (Actual)
Primary Completion Date
September 2006 (Actual)
Study Completion Date
December 2007 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CHU de Quebec-Universite Laval

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of the study is to evaluate the effect of daily oral intake of DHEA 50 mg for 4 months on reducing vasomotor symptoms (hot flashes) compared to placebo administration in postmenopausal women.
Detailed Description
Humans, along with the other primates, are unique among animal species in having adrenals that secrete large amounts of the inactive precursor steroids dehydroepiandrosterone (DHEA) and especially its sulfate DHEA-S. The marked reduction in the formation of DHEA-S by the adrenals during aging results in a dramatic fall in the formation of androgens and estrogens in peripheral target tissues, a situation that has been proposed to be associated with age-related diseases including skin atrophy, insulin resistance and obesity. Much attention has been given to the benefits of DHEA administered to postmenopausal women, especially on the bone, skin, vagina and well being after oral as well as percutaneous administration of the precursor steroid. This study proposes to study the effect of 50 mg oral DHEA capsules during a period of 4 months administered to postmenopausal women experiencing 50 or more moderate to severe hot flushes per week. Participants will be stratified by the number of hot flushes experienced per week. The two strata are: 50-70 or more than 70 hot flushes per week. During the study several biological and clinical parameters will be evaluated, as well as the reduction of the number of hot flashes and improvement of overall quality of life. Subjects will be evaluated at specific time intervals during the study for the above mentioned parameters as well as tolerability and adverse reactions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hot Flashes
Keywords
Hot Flashes, Menopause, Quality of Life, Hot flushes

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Experimental
Arm Title
DHEA
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Placebos
Intervention Description
Placebo capsule
Intervention Type
Drug
Intervention Name(s)
DHEA capsule
Intervention Description
One capsule of DHEA
Primary Outcome Measure Information:
Title
Use of a diary to monitor the number and intensity of hot flashes as compared to placebo at screening, day 1, weeks 2, 4, 8, 12 and 16
Secondary Outcome Measure Information:
Title
Evaluation of safety as well as quality of life, psychological general well being, and sexual life by questionnaires at day 1, 2, 4, 8, 12 and 16 weeks of treatment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy postmenopausal women with 50 or more moderate to severe hot flushes. Women between 40 to 70 years of age. Exclusion Criteria: Body mass index (BMI) of 35 kg/m2 or more. Significant metabolic and endocrine diseases. Diagnosis of cancer. Use of steroids or drugs that interfere with the metabolism of estrogen. Use of any systemic estrogen, progestin, or DHEA in the eight weeks prior to randomization. Use of alternative therapies or natural products to treat postmenopausal symptoms in the four weeks prior to randomization. Palpable fibroids or uterine prolapse: Grade 2 or 3. Cigarette smoking
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leonello Cusan, MD, PhD
Organizational Affiliation
CHUL Research Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Fernand Labrie, MD, PhD
Organizational Affiliation
CHUL Research Director
Official's Role
Study Director
Facility Information:
Facility Name
Clinique des Traitements Hormonaux
City
Sainte-Foy
State/Province
Quebec
ZIP/Postal Code
G1V 4G2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
11600526
Citation
Arlt W, Callies F, Koehler I, van Vlijmen JC, Fassnacht M, Strasburger CJ, Seibel MJ, Huebler D, Ernst M, Oettel M, Reincke M, Schulte HM, Allolio B. Dehydroepiandrosterone supplementation in healthy men with an age-related decline of dehydroepiandrosterone secretion. J Clin Endocrinol Metab. 2001 Oct;86(10):4686-92. doi: 10.1210/jcem.86.10.7974.
Results Reference
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PubMed Identifier
10626550
Citation
Baulieu EE. Neuroactive neurosteroids: dehydroepiandrosterone (DHEA) and DHEA sulphate. Acta Paediatr Suppl. 1999 Dec;88(433):78-80. doi: 10.1111/j.1651-2227.1999.tb14408.x.
Results Reference
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PubMed Identifier
7962278
Citation
Belanger A, Candas B, Dupont A, Cusan L, Diamond P, Gomez JL, Labrie F. Changes in serum concentrations of conjugated and unconjugated steroids in 40- to 80-year-old men. J Clin Endocrinol Metab. 1994 Oct;79(4):1086-90. doi: 10.1210/jcem.79.4.7962278.
Results Reference
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PubMed Identifier
8943786
Citation
Diamond P, Cusan L, Gomez JL, Belanger A, Labrie F. Metabolic effects of 12-month percutaneous dehydroepiandrosterone replacement therapy in postmenopausal women. J Endocrinol. 1996 Sep;150 Suppl:S43-50.
Results Reference
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PubMed Identifier
10323374
Citation
Flynn MA, Weaver-Osterholtz D, Sharpe-Timms KL, Allen S, Krause G. Dehydroepiandrosterone replacement in aging humans. J Clin Endocrinol Metab. 1999 May;84(5):1527-33. doi: 10.1210/jcem.84.5.5672.
Results Reference
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PubMed Identifier
14628495
Citation
Jedrzejuk D, Medras M, Milewicz A, Demissie M. Dehydroepiandrosterone replacement in healthy men with age-related decline of DHEA-S: effects on fat distribution, insulin sensitivity and lipid metabolism. Aging Male. 2003 Sep;6(3):151-6.
Results Reference
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PubMed Identifier
1838082
Citation
Labrie F. Intracrinology. Mol Cell Endocrinol. 1991 Jul;78(3):C113-8. doi: 10.1016/0303-7207(91)90116-a.
Results Reference
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PubMed Identifier
9253307
Citation
Labrie F, Belanger A, Cusan L, Gomez JL, Candas B. Marked decline in serum concentrations of adrenal C19 sex steroid precursors and conjugated androgen metabolites during aging. J Clin Endocrinol Metab. 1997 Aug;82(8):2396-402. doi: 10.1210/jcem.82.8.4160.
Results Reference
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PubMed Identifier
9329392
Citation
Labrie F, Diamond P, Cusan L, Gomez JL, Belanger A, Candas B. Effect of 12-month dehydroepiandrosterone replacement therapy on bone, vagina, and endometrium in postmenopausal women. J Clin Endocrinol Metab. 1997 Oct;82(10):3498-505. doi: 10.1210/jcem.82.10.4306.
Results Reference
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Citation
Labrie F, Simard J, Luu-The V, Belanger A, Pelletier G, Morel Y, Mebarki F, Sanchez R, Durocher F, Turgeon C, Labrie Y, Rheaume E, Labrie C, Lachance Y. The 3B-hydroxysteroid dehydrogenase/isomerase gene family: lessons from type II 3B-HSD congenital deficiency.In: Signal Transduction in Testicular Cells. Ernst Schering Research Foundation Workshop. Hansson, V., Levy, F.O. and Tasken, K. (eds.), Berlin, Heidelberg, New York, Springer-Verlag, Vol. Suppl. 2:pp. 185-218, 1996.
Results Reference
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Effect of Dehydroepiandrosterone (DHEA) on Hot Flashes in Postmenopausal Women

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