Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04064489
Other study ID # 49RC19_0027
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 16, 2020
Est. completion date February 4, 2022

Study information

Verified date August 2022
Source University Hospital, Angers
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Non-surgical traumas to the lower limbs that require orthopedic immobilisation (plaster or splint) are a frequent reason for going to accident and emergency. Due to venous stasis caused by immobilisation, hypercoagulable states and vascular injuries brought on by the trauma, these patients are at risk of developing VTE. For this reason, it is current practice in France and Belgium for the majority of patients to receive a preventative anticoagulant treatment. However, the benefit of this treatment, which has a considerable cost, is controversial. Contrary to French recommendations, American recommendations from 2012 actually advise against systematic preventative medicine, with prevention appearing to be effective primarily in studies with restrictive inclusion criteria. The most significant randomised controlled study on the subject did not show the benefit of low-molecular-weight heparin (LMWH) on the rate of symptomatic VTE among 1,435 non-selected patients. Therefore, in 2017, the Cochrane meta-analysis concluded that stratification of the risk of thromboembolism is required. For this purpose, in collaboration with the Dutch team of Nemeth et al. we have recently developed a risk stratification model that takes into consideration the patient's characteristics, the type of immobilisation and the severity of the trauma: the TRiP(cast) score. This score is applied retrospectively to a large cohort and demonstrates excellent prognostic performances (AUC (area under the curve) of 0.74). In addition, when using a <7 limits, it makes it possible to identify a large group of patients at very low risk of developing VTE (negative predictive value: 99.2%). The aim of the CASTING study is to prospectively demonstrate the reliability and utility of the TRiP(cast) score by showing that patients with orthopaedic immobilisation of a lower limb who are not receiving preventative treatment on the basis of a TRiP(cast) score of <7 have a very low rate of symptomatic VTE, which allows for a significant reduction in prescriptions of anticoagulants in comparison with prior practices.


Recruitment information / eligibility

Status Completed
Enrollment 2123
Est. completion date February 4, 2022
Est. primary completion date February 4, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Consultation in one of the emergency department participating in the study, - Isolated trauma from lower limb, - Rigid (plaster or resin) or semi-rigid immobilization for an assumed duration of at least 7 days, - Adults (18 years), - Affiliated patient or beneficiary of a social security, - Patient with prior informed consent. Exclusion Criteria: - Patient with anticoagulant treatment at the time of trauma, - Trauma requiring hospitalization of more than 48 hours, - Co-morbidity(s) requiring hospitalization of more than 48 hours at the time of inclusion, - Any factor making 90-day follow-up impossible, - Pregnant, nursing or childbearing patient, - Patient deprived of liberty by judicial or administrative decision, - Patient undergoing psychiatric care under duress, - Patient subject to a legal protection measure, - Patient unable to give free and informed consent.

Study Design


Intervention

Other:
TRIPscore
TRIPcast score calculation

Locations

Country Name City State
Belgium Clinique Universitaire Saint-Luc Bruxelles
France Centre Hospitalier d'Agen Agen
France CHU Angers Angers
France Centre Hospitalier de Cholet Cholet
France Centre Hospitalier Universitaire de Grenoble Grenoble
France Centre Hospitalier Le Mans Le Mans
France Centre Hospitalier Universitaire de Nantes Nantes
France Centre Hospitalier d'Orléans Orléans
France APHP Bichat Paris
France APHP Cochin Paris
France Centre Hospitalier Universitaire de Poitiers Poitiers
France Centre Hospitalier Universitaire de Rennes Rennes
France Centre Hospitalier de Saint-Brieuc Saint-Brieuc
France Centre Hospitalier Universitaire de Toulouse Toulouse
France Centre Hospitalier Universitaire de Tours Tours

Sponsors (15)

Lead Sponsor Collaborator
University Hospital, Angers Bichat Hospital, Centre Hospitalier d'Agen, Centre Hospitalier de Cholet, Centre Hospitalier de Saint-Brieuc, Centre Hospitalier le Mans, Centre Hospitalier Régional d'Orléans, CHU Rennes - Hopital Pontchaillou, Cliniques universitaires Saint-Luc- Université Catholique de Louvain, Hôpital Cochin, Nantes University Hospital, Poitiers University Hospital, University Hospital, Grenoble, University Hospital, Toulouse, University Hospital, Tours

Countries where clinical trial is conducted

Belgium,  France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Rate of symptomatic venous thromboembolic events (deep vein thrombosis and / or pulmonary embolism) among patients with a TRiP(cast) score < 7 To demonstrate the reliability and safety of the decision not to implement thromboprophylaxis in patients with orthopedic immobilization for lower extremity trauma and Trip(cast) < 7 Day 90
Secondary Rate of prescription for thromboprophylaxis comparison between the two period Day 1
Secondary Rate of symptomatic venous thromboembolic events (deep vein thrombosis and / or pulmonary embolism) (whole population) comparison between the two period Day 90
Secondary The rate of complications of preventive anticoagulant treatment (bleeding) comparison between the two period Day 90
Secondary The direct cost of preventive anticoagulant treatment when the TRiP(cast) score is applied compared to current practices treatment, nurse, blood test...cost of care Day 90
Secondary Physicians' satisfaction using likert's scale 5 level ladder : from totally unsatisfied to totally satisfied Day 1
See also
  Status Clinical Trial Phase
Recruiting NCT05347550 - Examining the Benefit of Graduated Compression Stockings in the Prevention of vEnous Thromboembolism in Low-risk Surgical Patients N/A
Enrolling by invitation NCT05794165 - Antithrombin to Improve Thromboprophylaxis and Reduce the Incidence of Trauma-Related Venous Thromboembolism Phase 2
Completed NCT02379806 - The SYMPTOMS - SYstematic Elderly Medical Patients Thromboprophylaxis: Efficacy on Symptomatic OutcoMeS - Study Phase 3
Recruiting NCT03691753 - Safety and Efficacy Study of Fitaya Vena Cava Filter N/A
Completed NCT02197416 - Safety of Dabigatran Etexilate in Blood Clot Prevention in Children Phase 3
Recruiting NCT05378035 - DOAC in Chinese Patients With Atrial Fibrillation
Recruiting NCT05171075 - A Study Comparing Abelacimab to Dalteparin in the Treatment of Gastrointestinal/Genitourinary Cancer and Associated VTE Phase 3
Completed NCT01895777 - Open Label Study Comparing Efficacy and Safety of Dabigatran Etexilate to Standard of Care in Paediatric Patients With Venous Thromboembolism (VTE) Phase 3
Completed NCT05897697 - Assessing Women's Preferences for Postpartum Thromboprophylaxis: the Prefer-Postpartum Study
Completed NCT04736719 - Replication of the AMPLIFY Anticoagulant Trial in Healthcare Claims Data
Completed NCT04736420 - Replication of the EINSTEIN-DVT Anticoagulant Trial in Healthcare Claims Data
Completed NCT04735523 - Replication of the RECOVER-II Anticoagulant Trial in Healthcare Claims Data
Completed NCT02746185 - Cancer Associated Thrombosis, a Pilot Treatment Study Using Rivaroxaban Phase 3
Completed NCT02912234 - Effect of Clarithromycin on the Pharmacokinetics of Apixaban in Healthy Participants Phase 1
Completed NCT02829957 - RAMBLE - Rivaroxaban vs. Apixaban for Heavy Menstrual Bleeding Phase 2/Phase 3
Completed NCT02334007 - Extended Low-Molecular Weight Heparin VTE Prophylaxis in Thoracic Surgery Phase 1/Phase 2
Completed NCT02223260 - Tolerability , PK/PD and Safety of Dabigatran Etexilate Oral Liquid Formulation in Children < 1 Year of Age Phase 2
Completed NCT02661568 - Description of Patients With Acute Venous Thromboembolism in the UK's Clinical Practice Research Datalink Linked With Hospital Episode Statistics Dataset (CPRD-HES) N/A
Completed NCT01976988 - Prospective Study on Preoperative Versus Postoperative Venous Thromboprophylaxis in Patients Undergoing Major Colorectal Surgery Phase 3
Completed NCT01972243 - Risk of Recurrent Venous Thrombosis: A Validation Study of the Vienna Prediction Model