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NCT00143754 Clinical Trial

Effect of Chronic Oral Hydration in Patients With Recurrent Unexplained Syncope

Hydration Clinical Trial

Official title:
Benefit of Controlled Rehydration in Unexplained Syncope

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT00143754
Other study ID # CP00-02
Secondary ID Centre Evian pou
Status Terminated
Phase Phase 3
First received August 31, 2005
Last updated August 31, 2005

Study information
Verified date August 2005
Source University Hospital, Angers
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

Beneficial effect of chronic hydration with salt supplementation in patients with recurrent unexplained syncope is not established. We sought to determine if chronic oral rehydration with salt supplementation improved the tolerance and hemodynamic responses of patients with unexplained recurrent syncope.

Recruitment information / eligibility
Status Terminated
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Syncopal and/or near syncopal episodes at least twice within the prior 3 months

Exclusion Criteria:

- Neurological disease

- Structural heart disease

- Metabolic and psychiatric illness

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind

Related Conditions & MeSH terms

Intervention

Procedure:
• Hydration

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University Hospital, Angers
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