MedPath

Impact of Vitamin C Supplementation on delirium

Phase 3
Recruiting
Conditions
Delirium.
Other delirium Delirium of mixed origin Postoperative delirium
F05.8
Registration Number
IRCT20080830001127N7
Lead Sponsor
Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
180
Inclusion Criteria

All adult patients between the ages of 18 and 75 and candidates for elective cardiac surgery

Exclusion Criteria

Previous use of anti-psychotic drugs
Surgeries that does not use a heart or lung pump
Previous use of anti-psychotic drugs
Patients who are not extubated until 5 days after surgery
Patients with mental retardation

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Delirium. Timepoint: Before entering the ICU, before the pump, during the pump, after the pump, the first day of the ICU, the second day of the ICU, the third day. Method of measurement: Using the Richmond Agitation-Sedation Scale criterion.;Intensity of delirium. Timepoint: Before entering the ICU, before the pump, during the pump, after the pump, the first day of the ICU, the second day of the ICU, the third day. Method of measurement: Using CAM-ICU confusion recognition and review tools.;Blood pressure. Timepoint: Before entering the ICU, before the pump, during the pump, after the pump, the first day of the ICU, the second day of the ICU, the third day. Method of measurement: Using a mercury barometer.;Laboratory variables (sodium and potassium and ABG variables). Timepoint: Before entering the ICU, before the pump, during the pump, after the pump, the first day of the ICU, the second day of the ICU, the third day of the ICU. Method of measurement: By taking blood and determining laboratory values.
Secondary Outcome Measures
NameTimeMethod
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