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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04155372
Other study ID # VGHKS19-CT7-08
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 2019
Est. completion date August 2020

Study information

Verified date November 2019
Source Kaohsiung Veterans General Hospital.
Contact JIAN-YU LIN
Phone 886-7-342-2121
Email linchainyu0822@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the present study is to investigate the effect of different rate of fluid consumption on post-exercise rehydration.


Description:

The body water deficits equivalent to 2% body mass might impair performance. Due to high exercise intensity, thermal environment, or rule limitation, athletes often in dehydration status post-exercise. Thus, how to rehydrate effectively to prepare the next game is important. The participants arrived to the lab euhydrated and were dehydrated to 2% of body weight by running. After a rest, they will ingest sports drink in a volume equivalent to 150% of BW loss in 30 min, 60 min, or 90 min. Urine and blood sample will be collected to evaluate hydration status.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date August 2020
Est. primary completion date July 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

- 20~35 years old male

- Exercise 150 min per week

- Without chronic disease or gastrointestinal surgery

Exclusion Criteria:

- Injury

- Answer "Yes" in part 1 of the Physical Activity Readiness Questionnaire(PAR-Q+)

- Participate in other studies within one month

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Different Fluid Ingestion Rate
The participants ingested sports drink in a volume equivalent to 150% of BW loss, in 30 min, 60 min, or 90min.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Kaohsiung Veterans General Hospital. Kaohsiung Medical University

Outcome

Type Measure Description Time frame Safety issue
Primary specific gravity of urine(SG) dehydration: >= 1.020 Change from baseline outcome measure at dehydration and 1st and 2nd hour in recovery period
Primary Osmolality(Urine) dehydration: >= 700 mosm/kg Change from baseline outcome measure at dehydration and 1st and 2nd hour in recovery period
Primary Osmolality(Blood) dehydration: >= 290 mosm/kg Change from baseline outcome measure at dehydration and 1st and 2nd hour in recovery period
Primary Vasopressin Vasopressin, also called antidiuretic hormone (ADH), arginine vasopressin (AVP) or argipressin, is a hormone synthesized as a peptide prohormone in neurons in the hypothalamus, and is converted to AVP. Increasing the water reabsorption and excretion of more concentrated urine. Change from baseline outcome measure at dehydration and 1st and 2nd hour in recovery period
Primary sodium(blood) 135~145mEq/L Change from baseline outcome measure at dehydration and 1st and 2nd hour in recovery period
Primary Body weight change measure body weight at baseline, dehydration, 1st and 2nd hour in recovery period in kg Change from baseline outcome measure at dehydration and 1st and 2nd hour in recovery period
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