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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02980939
Other study ID # 16-10-135
Secondary ID
Status Completed
Phase N/A
First received November 30, 2016
Last updated May 27, 2017
Start date November 2016
Est. completion date March 18, 2017

Study information

Verified date May 2017
Source University of Arkansas, Fayetteville
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

During exercise in the heat, there is a need to replenish fluids in order to avoid dehydration and decrease the risk for heat illness. What drives this urge to drink is the thirst mechanism. Following ingestion of fluids, there is an inhibition of thirst before there is a replenishing of fluids. However, there is little scientific evidence of where thirst is inhibited, if this thirst inhibition is augmented by exercise and how thirst itself influence exercise performance. Further, during rehydration studies, it is very difficult to successfully blind a subject to their drinking/hydration protocol. Previous studies that have blinded a subject to their drinking have used various methods such as intravenous fluid administration and/or nasogastric tubes. Therefore, the purpose of this research is to examine the mechanistic roles thirst inhibition plays while exercising in the heat while undergoing intravenous fluid administration. Specific attention will be directed to the cardiovascular and thermoregulatory function of the individuals. All blood, cardiovascular, thermoregulatory, and perceptual measures are shown in the diagram below.


Recruitment information / eligibility

Status Completed
Enrollment 11
Est. completion date March 18, 2017
Est. primary completion date March 18, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- Cycling Racing History category 3 or higher USA cycling certification

- maximal oxygen uptake >55 ml/kg/min

Exclusion Criteria:

- History of heat stroke

- Renal, cardiovascular, metabolic diseases

- Regular medication

Study Design


Related Conditions & MeSH terms


Intervention

Other:
iv fluid infusion
Intravenous isotonic saline infusion

Locations

Country Name City State
United States University of Arkansas - HPER Fayetteville Arkansas

Sponsors (1)

Lead Sponsor Collaborator
University of Arkansas, Fayetteville

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 5km - Cycling Time Trial Time to completion 5 km cycling time trial in the heat 2hour
Secondary Rectal Temperature Body core temperature at the end of the 5 km time trial 2hour
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