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NCT00581373 Clinical Trial

Water and the Gastropressor Response - Diurnal Variability

Orthostatic Hypotension Clinical Trial

Official title:
Water and the Gastropressor Response - Diurnal Variability (Specific Aim 1.3)

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00581373
Other study ID # 060553
Secondary ID Vanderbilt Disco
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date August 2007
Est. completion date December 2025

Study information
Verified date September 2023
Source Vanderbilt University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

We will test the null hypothesis that there is no diurnal (morning to afternoon)variability in the blood pressure response to the ingestion of water 16 oz.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 20
Est. completion date December 2025
Est. primary completion date December 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria: - orthostatic intolerance Exclusion Criteria: - pregnancy

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• water 16 fl oz
water 16 fl oz in AM and repeat in late afternoon

Locations
Country Name City State
United States Vanderbilt University Nashville Tennessee

Sponsors (1)
Lead Sponsor Collaborator
Satish R. Raj

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary blood pressure 1 day
Secondary heart rate 1 day
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