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The Effect of Ascorbic Acid on the blood loss in Total Hip Arthroplasty

Not Applicable
Recruiting
Conditions
Total Hip Arthroplasty.
Unilateral primary osteoarthritis of hip
M16.1
Registration Number
IRCT20221104056393N2
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
70
Inclusion Criteria

Candidates of total hip arthroplasty due to osteoarthritis
Patients who provide written informed consent to participate in this study.

Exclusion Criteria

history of thromboembolic events like deep vein thrombosis or pulmonary embolism
history of cardiovascular disease like myocardial infarction or atrialfibrillation
clotting disorders including abnormal PT, PTT or INR
being in pregnancy or in the lactation period
drug abusers or alcoholics
severe renal dysfunction
severe infection
the preoperative hemoglobin of < 10 g/dL
diagnosis of inflammatory arthritis like rheumatoid arthritis, pigmented villonodular synovitis and etc

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total blood loss. Timepoint: Before intervention, 24h after intervention. Method of measurement: amount of Hemoglobin drop.
Secondary Outcome Measures
NameTimeMethod
Transfusion rate. Timepoint: Before the intervention, 24h after the intervention. Method of measurement: number of units of blood transfused.
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