Condition: Knee Osteoarthritis · Sponsor: Peking University Third Hospital
The study subjects are patients in our hospital's orthopedics department undergoing unilateral primary total knee arthroplasty (TKA) due to primary osteoarthritis. Through a prospective, parallel randomized controlled study, 112 participants will be divided into two groups: the SURGICEL® Powder group and the non-use group. The study will compare the total perioperative blood loss , intraoperative blood loss, transfusion rate and volume, postoperative hemoglobin decline, hematocrit decline, limb swelling rate , postoperative limb pain , and range of motion. Statistical analysis will be performed on the data to observe the hemostatic effects of SURGICEL® Powder, providing recommendations for the clinical use of SURGICEL® Powder.
This description comes directly from the study's public registry record.
Hua Tian, doctor · 86-18811185091 · tianhua@bjmu.edu.cn
Guo Wei Zhang, bachelor · 86-18811778038 · 2011210412@pku.edu.cn
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| Peking University Third Hospital | Beijing, Beijing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06608992