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The Effects of Estradiol and Progesterone on Arginine Vasopressin Regulation and Serum Sodium Concentration

Primary Purpose

Exercise Induced Hyponatremia

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Gatorade Endurance Formula
ganirelix acetate
Sponsored by
Yale University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Exercise Induced Hyponatremia

Eligibility Criteria

18 Years - 35 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • healthy volunteers (18-35 yrs) with and without previous exercise induced hyponatremia

Exclusion Criteria:

  • conditions that would preclude safe exercise or safe use of hormones

Sites / Locations

  • John B. Pierce Laboratory

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

type of beverage

Outcomes

Primary Outcome Measures

osmotic regulation of AVP

Secondary Outcome Measures

temperature responses

Full Information

First Posted
January 2, 2008
Last Updated
March 27, 2020
Sponsor
Yale University
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1. Study Identification

Unique Protocol Identification Number
NCT00589134
Brief Title
The Effects of Estradiol and Progesterone on Arginine Vasopressin Regulation and Serum Sodium Concentration
Official Title
The Effects of Estradiol and Progesterone on Arginine Vasopressin Regulation and Serum Sodium Concentration
Study Type
Interventional

2. Study Status

Record Verification Date
July 2010
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
December 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Yale University

4. Oversight

5. Study Description

Brief Summary
Women are at greater risk for exercise-induced hyponatremia (low blood sodium concentration) and this risk has been attributed to their lower body weight and size, excess water ingestion and longer racing times relative to men. While these factors contribute to the greater incidence of hyponatremia in women, it is likely that their greater levels of estradiol in plasma and/or tissue also play a role in increasing the risk of hyponatremia in women. More importantly, estradiol may also leave women more susceptible to the extreme consequences of hyponatremia (i.e. brain damage, death). Hyponatremia is generally attributed to inappropriately elevated levels of the hormone arginine vasopressin (AVP). AVP is the most important hormone controlling water retention in the kidney. Earlier studies in our laboratory have demonstrated that estradiol lowers the threshold for thirst sensation and AVP release during exercise. The purpose of these studies is to test the hypotheses that in women with a history of hyponatremia, estradiol lowers the thresholds for thirst and AVP release, leading to greater fluid retention, lower blood sodium concentration during endurance exercise in the heat. However, we further hypothesize that progesterone administration along with estradiol administration will attenuate the effect of estradiol on the regulation of thirst and AVP, normalize fluid retention, and serum sodium concentration during endurance exercise in the heat. In women without a history of hyponatremia, we expect that estradiol administration will lower the thresholds for thirst and AVP release, but will not increase fluid retention or reduce blood sodium concentration during endurance exercise in the heat. We hypothesize that progesterone administration along with estradiol administration will attenuate the effect of estradiol on thirst and AVP, but have no effect on fluid retention or serum sodium concentration during endurance exercise in the heat. To test these hypotheses, women will perform endurance exercise in the heat under three hormonal conditions: 1) during Gonadotropin-releasing hormone (GnRH) antagonist alone--which will suppress estradiol and progesterone; 2) during GnRH antagonist+estradiol; and 3) during GnRH antagonist+estradiol+ progesterone. During exercise, fluid will be replaced with either water or a carbohydrate-electrolyte beverage (random assignment).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Exercise Induced Hyponatremia

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
type of beverage
Intervention Type
Dietary Supplement
Intervention Name(s)
Gatorade Endurance Formula
Intervention Description
carbohydrate electrolyte beverage
Intervention Type
Other
Intervention Name(s)
ganirelix acetate
Other Intervention Name(s)
Antagon
Intervention Description
GnRH antagonist, subcutaneous injection, 0.25 mg/day for 21 days.
Primary Outcome Measure Information:
Title
osmotic regulation of AVP
Time Frame
3 years
Secondary Outcome Measure Information:
Title
temperature responses
Time Frame
3 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: healthy volunteers (18-35 yrs) with and without previous exercise induced hyponatremia Exclusion Criteria: conditions that would preclude safe exercise or safe use of hormones
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nina Stachenfeld, PhD
Organizational Affiliation
John B. Pierce Laboratory
Official's Role
Principal Investigator
Facility Information:
Facility Name
John B. Pierce Laboratory
City
New Haven
State/Province
Connecticut
ZIP/Postal Code
06519
Country
United States

12. IPD Sharing Statement

Learn more about this trial

The Effects of Estradiol and Progesterone on Arginine Vasopressin Regulation and Serum Sodium Concentration

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