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evaluation of the effect of pre-hydration on the fatigue and exhaustion of patients undergoing plasma therapy

Not Applicable
Recruiting
Conditions
patient undergoing plasmapheresis.
Autoimmune disease (systemic) NOS
Registration Number
IRCT20170812035650N2
Lead Sponsor
Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
30
Inclusion Criteria

Be to Iran
dont be addicted
to not use housing

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Fatigue. Timepoint: during and after plasmapheresis. Method of measurement: with scale.;Thirst. Timepoint: during and after plasmapheresis. Method of measurement: with scale.
Secondary Outcome Measures
NameTimeMethod
Blood presure. Timepoint: during plasmapheresis. Method of measurement: Barometer.
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