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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


Intervention

Procedure:
Hydration


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Angers
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