Effect of Chronic Oral Hydration in Patients With Recurrent Unexplained Syncope

NCT ID: NCT00143754

Last Updated: 2005-09-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE3

Study Classification

INTERVENTIONAL

Brief Summary

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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.

Detailed Description

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Conditions

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Hydration Loss of Consciousness Neurocardiogenic Syncope

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Blinding Strategy

SINGLE

Interventions

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Hydration

Intervention Type PROCEDURE

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Angers

OTHER_GOV

Sponsor Role lead

Principal Investigators

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Georges PN Leftheriotis, MD-PhD

Role: PRINCIPAL_INVESTIGATOR

HUAngers

Other Identifiers

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Centre Evian pour l'Eau

Identifier Type: -

Identifier Source: secondary_id

CP00-02

Identifier Type: -

Identifier Source: org_study_id