Effects of Femoral Canal Opening Technique on Biomarkers
Effects of Femoral Canal Opening Technique on Inflammation, Coagulation, Organ Dysfunction, and Bone Metabolism
This single-centre prospective randomized study consisted of 60 participants (50 women) with a mean age of 80.33 ± 11.13 years, randomly allocated to either manual medullary canal opening (n = 30) or mechanical drilling of the canal (n = 30). Outcomes were assessed preoperatively and postoperatively during a 72-hour follow-up period. This study had a prospective design. Outcomes were assessed preoperative and during the follow-up period to 72 hours after surgery. During follow-up, all patients underwent laboratory testing. Blood samples were collected 2 hours preoperatively and 72 hours postoperatively in order to determine blood concentrations of leukocytes, erythrocytes, platelets (×10⁹/L), haemoglobin (g/L), D-dimers (IU/L), prothrombin time, international normalized ratio (INR), activated partial thromboplastin time (aPTT) (s), aPTT ratio, fibrinogen (g/L), creatinine (μmol/L), N-terminal pro-B-type natriuretic peptide (NT-proBNP) (pg/mL), C-reactive protein (CRP) (mg/L), glucose, urea, sodium, potassium, chloride, calcium, and phosphorus (mmol/L), as well as bone metabolism markers: total procollagen type 1 N-terminal propeptide (tP1NP) (µg/L), N-min osteocalcin (N-mOST) (µg/L), C-terminal telopeptide of type I collagen (β-CTX) (ng/mL), and bone-specific alkaline phosphatase (BAP) (µg/L).
The investigatoras compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours. In addition, the investigators analysed the dynamics (baseline vs. 72 hours) of outcome measures between the two study groups.
調査の概要
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
-
-
-
Split、クロアチア
- University Hospital of Split, 21000 Croatia
-
-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- adult patients (aged > 18 years) admitted to the Department of Surgery, Orthopaedics and Traumatology Division, University Hospital Centre Split, who, during the observation period, sustained a pertrochanteric femoral fracture following a fall and were scheduled for surgery within 3 days after injury.
Exclusion Criteria:
- included patients with acute or chronic inflammatory conditions
- polytraumatic patients
- patients with disseminated malignant disease
- acute organ failure
- patients on vitamin D and calcium supplementation
- patients receiving corticosteroids, cytostatics, anticoagulations, or other medications that could influence the observed parameters.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:診断
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:独身
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
他の:manual medullary canal opening
Tthe medullary canal was opened under fluoroscopic guidance using a cannulated curved awl (14.0/3.2 mm).
|
All participants were operated on according to the same protocol, using the same type of procedure on a traction table, with prior fracture reduction under fluoroscopic (X-ray) guidance.
All patients had the same type of fracture (pertrochanteric femoral fracture), and intramedullary osteosynthesis was performed using a ⌀ 9.0 mm, 340 mm Proximal Femoral Nail Antirotation (PFNA) (Synthes GmbH, Oberdorf, Switzerland).
In the first group, the medullary canal was opened under fluoroscopic guidance using a cannulated curved awl (14.0/3.2 mm).
In the second group, the medullary canal was opened under fluoroscopic guidance using a battery-powered surgical drill equipped with a cannulated drill bit (13.0 mm diameter, 290 mm length) (Synthes GmbH, Oberdorf, Switzerland).
|
|
他の:mechanical drilling of the canal
The medullary canal was opened under fluoroscopic guidance using a battery-powered surgical drill equipped with a cannulated drill bit (13.0 mm diameter, 290 mm length)
|
All participants were operated on according to the same protocol, using the same type of procedure on a traction table, with prior fracture reduction under fluoroscopic (X-ray) guidance.
All patients had the same type of fracture (pertrochanteric femoral fracture), and intramedullary osteosynthesis was performed using a ⌀ 9.0 mm, 340 mm Proximal Femoral Nail Antirotation (PFNA) (Synthes GmbH, Oberdorf, Switzerland).
In the first group, the medullary canal was opened under fluoroscopic guidance using a cannulated curved awl (14.0/3.2 mm).
In the second group, the medullary canal was opened under fluoroscopic guidance using a battery-powered surgical drill equipped with a cannulated drill bit (13.0 mm diameter, 290 mm length) (Synthes GmbH, Oberdorf, Switzerland).
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
The main marker od inflamation
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
CRP (mg/L)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Blood cells count
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
blood concentrations of leukocytes, erythrocytes, platelets (×10⁹/L)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
|
D-dimers concetration
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
D-dimers (IU/L)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
|
Coagulation: prothrombin time with international normalized ratio (INR)
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
prothrombin time (seconds)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
|
Coagulation: activated partial thromboplastin time (aPTT)
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
activated partial thromboplastin time (aPTT) (seconds)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
|
Fibrinogen concentration
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
fibrinogen (g/L)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
|
Creatinine concentration
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
creatinine (μmol/L)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
|
Concetration of N-terminal pro-B-type natriuretic peptide (NT-proBNP)
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
N-terminal pro-B-type natriuretic peptide (NT-proBNP) (pg/mL)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
|
Plasma biochemistry
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
glucose, urea, sodium, potassium, chloride, calcium, and phosphorus (mmol/L)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
|
Bone metabolism markers
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
total procollagen type 1 N-terminal propeptide (tP1NP) (µg/L), N-min osteocalcin (N-mOST) (µg/L), bone-specific alkaline phosphatase (BAP) (µg/L)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
|
Bone metabolism marker C-terminal telopeptide of type I collagen (β-CTX)
時間枠:The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
C-terminal telopeptide of type I collagen (β-CTX) (ng/mL)
|
The investigators compared differences in blood parameters between the two groups at baseline, as well as differences after 72 hours.
|
協力者と研究者
捜査官
- 主任研究者:Vedran Kovacic、University of Split, School of Medicine
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- 520-03/25-01/65
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。