Unique ID issued by UMIN | UMIN000029797 |
---|---|
Receipt number | R000033781 |
Scientific Title | Intravenous versus combined intravenous and intra-articular tranexamic acid for simultaneous bilateral total hip arthroplasty: randomized controlled trial |
Date of disclosure of the study information | 2017/11/02 |
Last modified on | 2019/03/23 09:27:39 |
Intravenous versus combined intravenous and intra-articular tranexamic acid for simultaneous bilateral total hip arthroplasty: randomized controlled trial
Intravenous versus combined intravenous and intra-articular tranexamic acid for simultaneous bilateral total hip arthroplasty: randomized controlled trial
Intravenous versus combined intravenous and intra-articular tranexamic acid for simultaneous bilateral total hip arthroplasty: randomized controlled trial
Intravenous versus combined intravenous and intra-articular tranexamic acid for simultaneous bilateral total hip arthroplasty: randomized controlled trial
Japan |
Osteoarthritis of the hip, Avascular necrosis of the femoral head, Rheumatoid arthritis
Orthopedics |
Others
NO
To evaluate whether combined intravenous and intra-articular administration of tranexamic acid reduced perioperative blood loss compared with intravenous-only administration of tranexamic acid for the patients undergoing simultaneous bilateral total hip arthroplasty.
Safety
The volume of perioperative blood loss measured using the calculated blood volume and change in hemoglobin from preoperative to postoperative day 4.
Complication
Interventional
Parallel
Randomized
Individual
Double blind -all involved are blinded
Placebo
NO
NO
NO
2
Treatment
Medicine |
The combined tranexamic acid group received 1000 mg of tranexamic acid administered intravenously just before skin incision of the first hip. After closure of fascia, 1000 mg of tranexamic acid (10 mL of 100 mg/mL tranexamic acid) was administered intra-articularly for each hip. Five hours after the first intravenous administration of tranexamic acid, 1000 mg of tranexamic acid was again given intravenously.
The intravenous tranexamic acid group received 1000 mg of tranexamic acid administered intravenously just before skin incision of the first hip. After closure of the fascia, 10 mL of normal saline was administered intra-articularly for each hip. Five hours after the first intravenous administration of tranexamic acid, 1000 mg of tranexamic acid was again given intravenously.
18 | years-old | <= |
Not applicable |
Male and Female
Patients undergoing simultaneous bilateral total hip arthroplasty
Known allergic reaction to tranexamic acid
Refusal of blood products
40
1st name | |
Middle name | |
Last name | Kenji Kurosaka |
Hokusuikai Kinen Hospital
Orthopaedic Surgery
3-2-1 Higashihara, Mito, Ibaraki 310-0035, Japan
0293033003
kenjikurosaka@yahoo.co.jp
1st name | |
Middle name | |
Last name | Kenji Kurosaka |
Hokusuikai Kinen Hospital
Orthopaedic surgery
3-2-1 Higashihara, Mito, Ibaraki, 310-0035 Japan
029-303-3003
kenjikurosaka@yahoo.co.jp
Hokusuikai Kinen Hospital
Hokusuikai Kinen Hospital
Self funding
NO
2017 | Year | 11 | Month | 02 | Day |
Unpublished
Completed
2017 | Year | 09 | Month | 21 | Day |
2017 | Year | 09 | Month | 21 | Day |
2017 | Year | 11 | Month | 02 | Day |
2019 | Year | 03 | Month | 23 | Day |
2017 | Year | 11 | Month | 01 | Day |
2019 | Year | 03 | Month | 23 | Day |
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000033781