Revision Total Hip Replacement Arthroplasty and Hematologic Variables
Completed
- Conditions
- Avascular Necrosis of HipDegenerative Hip Joint Disease
- Interventions
- Other: RTHRA group
- Registration Number
- NCT02951741
- Lead Sponsor
- Seoul National University Bundang Hospital
- Brief Summary
Revision total hip replacement arthroplasty is a surgery having intra- and postoperative substantial blood loss. The investigators will investigate the relationship between the various hematologic variables and postoperative bleeding volume.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 62
Inclusion Criteria
- revision total hip replacement
Exclusion Criteria
- hematologic disease
- anticoagulant medication
- American Society of Anesthesiologists physical status 4 and 5
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description RTHRA group RTHRA group patients undergoing revision total hip replacement
- Primary Outcome Measures
Name Time Method Change of FIBTEM 5 minutes before initiation of anesthesia and 5 minutes after finishing operation FIBTEM: one of the measurements of the rotational thromboelastometry
- Secondary Outcome Measures
Name Time Method Hemoglobin postoperative day 4 postoperative bleeding volume postoperative 72 hours volume of infused fluid during operation Period from starting to finishing the operation (During operation, an expected average of 3 hours) Infused total crystalloid and colloid volume during the operation will be recorded
intraoperative urine output Period from starting to finishing the operation (During operation, an expected average of 3 hours) transfusion units Period from starting to finishing the operation (During operation, an expected average of 3 hours) and postoperative first day Red blood cell
Hematocrit postoperative day 4 Platelet count postoperative day 4 prothrombin time_international normalized ratio postoperative day 1 activated partial prothrombin time postoperative day 1 fibrinogen concentration postoperative day 1
Trial Locations
- Locations (1)
Seoul National University Bundang Hospital
🇰🇷Seongnam-si, Gyeonggi-do, Korea, Republic of