NCT02379806

Brief Summary

Venous thromboembolism (VTE) is a frequent condition, affecting 1.8 per 1,000 people every year. Admission to hospital is one of the main risk factors for VTE, and could account for up to 20% of all VTE, making VTE prevention in admitted patients an appealing option to reduce VTE global burden. The landmark MEDENOX trial and others demonstrated the efficacy of low molecular weight heparins (LMWH) in reducing a composite outcome of symptomatic and asymptomatic events, the latter accounting for the vast majority of events. Publication of these trials led to the implementation of thromboprophylaxis policies in hospitals, which acceptance has been variable. More recently, the use of thromboprophylaxis has been challenged after the publication of 1) a negative trial that used 'death from any cause' as main outcome, 2) a systematic review showing the lack of a clear efficacy on the risk of pulmonary embolism or death, 3) negative trials using new oral anticoagulants, 4) the last version of the American College of Chest Physicians Guidelines, focusing on symptomatic events only, downgraded its recommendation for thromboprophylaxis in medical patients to a 1B recommendation, restricting its use to patients 'at increased risk of thrombosis' and recommending against the use of thromboprophylaxis in patients at low risk of thrombosis, patients bleeding or at high risk of bleeding. However, a limitation of this interpretation of the data is that in most trials, patients with screened asymptomatic events were treated with anticoagulants, preventing the occurrence of symptomatic events during follow-up. Moreover, subgroup analyses showed that elderly patients were at high risk of thrombosis in these trials, and that LMWH could be particularly efficient in this subgroup of patients. Conversely, their risk of bleeding is also higher than in younger patients and the current trials were not powered to detect a difference in the bleeding risk between groups. Finally, the diagnostic and therapeutic management of VTE is more challenging in the elderly. Therefore, we planned a randomized controlled trial on the efficacy of LMWH for the prevention of symptomatic VTE in elderly patients.

Trial Health

90
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,560

participants targeted

Target at P75+ for phase_3

Timeline
Completed

Started Sep 2015

Longer than P75 for phase_3

Geographic Reach
2 countries

46 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 16, 2015

Completed
17 days until next milestone

First Posted

Study publicly available on registry

March 5, 2015

Completed
6 months until next milestone

Study Start

First participant enrolled

September 3, 2015

Completed
5.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2020

Completed
28 days until next milestone

Study Completion

Last participant's last visit for all outcomes

December 29, 2020

Completed
Last Updated

July 5, 2022

Status Verified

June 1, 2022

Enrollment Period

5.2 years

First QC Date

February 16, 2015

Last Update Submit

June 30, 2022

Conditions

Outcome Measures

Primary Outcomes (1)

  • Occurence of the following events: symptomatic confirmed deep venous thrombosis (DVT), symptomatic confirmed pulmonary embolism (PE), or fatal PE

    Occurence of any of the events through the Day 30 visit

Secondary Outcomes (1)

  • Occurence of the following events: Major bleeding, clinically relevant non major bleeding, symptomatic confirmed VTE (DVT or PE) or fatal PE, atherothrombotic cardiovascular events, cardiovascular death, Death from any cause.

    Occurence of any of the events through the Day 30 and Day 90 visit

Study Arms (2)

Active enoxaparin 40 mg

ACTIVE COMPARATOR

One 0.4 ml prefilled syringe containing 40 mg enoxaparin active substance administered once daily for 10 ± 4 days

Drug: Enoxaparin

Placebo of enoxaparin 40 mg

PLACEBO COMPARATOR

One 0.4 ml placebo syringe of enoxaparin 40 mg administered once daily for 10 ± 4 days

Drug: Placebo

Interventions

Also known as: Lovenox
Active enoxaparin 40 mg
Placebo of enoxaparin 40 mg

Eligibility Criteria

Age70 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

You may qualify if:

  • Patient aged 70 years or older
  • Admitted to hospital for an acute medical illness
  • Anticipated duration of hospitalization of at least 4 days
  • Life expectancy of at least 3 months

You may not qualify if:

  • Admission for one of the following reasons:
  • Planned medical procedure.
  • Routine health assessment requiring admission for baseline/trending of health status (e.g., routine colonoscopy).
  • Admission encountered for another life circumstance that causes no bearing on health status and requires no medical intervention (e.g., lack of housing, economic inadequacy, care-giver respite, family circumstances, administrative).
  • Hypersensitivity to heparin
  • History of Heparin Induced Thrombocytopenia
  • Active bleeding
  • Bacterial endocarditis
  • Platelet count of less than 80,000 per cubic millimeter
  • Patients who require anticoagulant therapy for any indication, and those who received any type of anticoagulant therapy for \> 48 hours
  • Organic lesion prone to bleeding.
  • Hemorrhagic events or bleeding tendency due to hemostasis disorders.
  • Concomitant use of aspirin (\> 160 mg/day), clopidogrel (\> 75 mg/day), or of combined antiplatelet therapy
  • Creatinine clearance \< 15 ml/min
  • Unable or unwilling to consent
  • +2 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (46)

Centre Hospitalier d'Agen

Agen, 47000, France

Location

CHU Angers

Angers, 49000, France

Location

CH Angoulême

Angoulême, 16959, France

Location

CH d'Arras

Arras, 62022, France

Location

CH Béthune

Béthune, 62400, France

Location

Hôpital Jean Verdier (APHP)

Bondy, 93143, France

Location

CHU Bordeaux

Bordeaux, 33075, France

Location

HIA Clermont-Tonnerre

Brest, 29200, France

Location

CHRU Brest

Brest, 29609, France

Location

CH Public du Cotentin

Cherbourg, 50102, France

Location

CH Louis Mourier de Colombes

Colombes, 97200, France

Location

CHU de Dijon

Dijon, 21000, France

Location

CHU Grenoble

Grenoble, 38700, France

Location

CHD Vendée

La Roche-sur-Yon, 85925, France

Location

Groupe Hospitalier Le Havre

Le Havre, France

Location

CHU Rouen

Le Petit-Quevilly, 76140, France

Location

CHRU de Lille

Lille, 59000, France

Location

CHU Limoges

Limoges, 87042, France

Location

CHD Vendée - Site de Luçon

Luçon, 85400, France

Location

Hôpital Edouard Herriot - CHU Lyon

Lyon, 69003, France

Location

CHU Lyon

Lyon, 69495, France

Location

Hôpital de la Timone - AP-HM

Marseille, 13274, France

Location

Clinique Mutualiste Médico-chirurgical "Beau Soleil"

Montpellier, France

Location

CH des Pays de Morlaix

Morlaix, 29600, France

Location

CHU Nancy

Nancy, 54035, France

Location

CHU de Nantes

Nantes, 44000, France

Location

Hôpital Cimiez - CHU Nice

Nice, 03003, France

Location

HEGP - Paris

Paris, 75000, France

Location

Hôpital Lariboisiere

Paris, 75000, France

Location

Hôpital Saint-Antoine (APHP)

Paris, 75012, France

Location

Hôpital Broca- APHP

Paris, 75013, France

Location

Hôpita Cochin - APHP

Paris, 75014, France

Location

Institut Mutualiste Montsouris

Paris, 75014, France

Location

CH Périgueux

Périgueux, 24019, France

Location

CHU Poitiers

Poitiers, 86021, France

Location

CH de Cornouaille - Quimper

Quimper, 29107, France

Location

CHU Rennes

Rennes, 35203, France

Location

Hôpital Charles Nicolle- CHU Rouen

Rouen, 76230, France

Location

CHU La Réunion - Site Félix Guyon

Saint-Denis, 97411, France

Location

CHU de Saint Etienne

Saint-Etienne, 42000, France

Location

CHU La Réunion - site du GHSR

Saint-Pierre, 97410, France

Location

CHRU Strasbourg- Service HTA et Maladies Vasculaires

Strasbourg, 67091, France

Location

CHU Strasbourg - Service de Médecine Interne

Strasbourg, 67091, France

Location

CH Intercommunal Toulon La Seyne sur Mer

Toulon, 83056, France

Location

HIA Sainte-Anne Toulon

Toulon, 83800, France

Location

Hôpitaux Universitaires de Genève

Geneva, 1211, Switzerland

Location

Related Publications (1)

  • Mottier D, Girard P, Couturaud F, Lacut K, Le Moigne E, Paleiron N, Guellec D, Sanchez O, Cogulet V, Laporte S, Marhic G, Mismetti P, Presles E, Robert-Ebadi H, Mahe I, Plaisance L, Reny JL, Darbellay Farhoumand P, Cuvelier C, Le Henaff C, Lambert Y, Danguy des Deserts M, Rousseau Legrand C, Boutreux S, Bleher Y, Decours R, Trinh-Duc A, Armengol G, Benhamou Y, Daumas A, Guyot SL, De Carvalho H, Lamia B, Righini M, Meyer G, Le Gal G. Enoxaparin versus Placebo to Prevent Symptomatic Venous Thromboembolism in Hospitalized Older Adult Medical Patients. NEJM Evid. 2023 Aug;2(8):EVIDoa2200332. doi: 10.1056/EVIDoa2200332. Epub 2023 Jun 27.

MeSH Terms

Conditions

Venous Thromboembolism

Interventions

Enoxaparin

Condition Hierarchy (Ancestors)

ThromboembolismEmbolism and ThrombosisVascular DiseasesCardiovascular Diseases

Intervention Hierarchy (Ancestors)

Heparin, Low-Molecular-WeightHeparinGlycosaminoglycansPolysaccharidesCarbohydrates

Study Design

Study Type
interventional
Phase
phase 3
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, INVESTIGATOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 16, 2015

First Posted

March 5, 2015

Study Start

September 3, 2015

Primary Completion

December 1, 2020

Study Completion

December 29, 2020

Last Updated

July 5, 2022

Record last verified: 2022-06

Locations