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Completed

NCT Number: NCT00203658

Assessment of Long-Term Out-of-Hospital Treatment of Patients With Proximal Deep Vein Thrombosis (DVT) Using Low-Molecular-Weight Heparin (LMWH) Versus LMWH Followed by Warfarin

The purpose of this study is to assess the long-term out-of-hospital treatment of patients with proximal venous thrombosis through the administration of subcutaneous low-molecular-weight heparin (tinzaparin sodium) versus low-molecular-weight heparin followed by warfarin sodium.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Thrombosis Research Unit, University of Calgary

Calgary, Alberta, T2N 2T9, Canada

About this study

Two studies demonstrated that out-of-hospital low-molecular-weight heparin given by twice daily subcutaneous injection without laboratory monitoring was as effective and as safe as continuous intravenous heparin given in-hospital. Innohep (tinzaparin) has been shown to be safe and effective for both the initial and long-term treatment of DVT. The Home LITE study compares long-term Innohep treatment to treatment with a combination of initial low-molecular-weight heparin followed by standard long-term warfarin therapy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients having a first or recurrent episode of acute proximal vein thrombosis who are eligible for outpatient or home care during the initial therapy.

Exclusion criteria

  • Any condition which, in the opinion of the investigator, precludes entire out-of-hospital treatment
  • Presence of familial bleeding diathesis or the presence of active bleeding contraindicating anticoagulant therapy
  • Receiving therapeutic heparin for more than 48 hours or have already been on warfarin for more than 2 days for the treatment of proximal deep vein thrombosis
  • Receiving long-term warfarin treatment
  • Females who are pregnant
  • Known allergy to heparin, warfarin sodium, or bisulfites
  • History of heparin-associated thrombocytopenia
  • Severe malignant hypertension
  • Hepatic encephalopathy
  • Severe renal failure
  • Inability to attend follow-up due to geographic inaccessibility
  • Inability or refusal to give signed informed consent
  • Mothers who are breast-feeding and who are unable to refuse to discontinue breast-feeding during study treatment

Treatment and study plan

Tinzaparin sodium

Drug

Primary outcomes

  1. objectively documented recurrent venous thromboembolism during initial treatment or during the 12 week follow-up period

  2. death during initial treatment or during the 12 week follow-up period

  3. safety endpoint for assessing harm was the occurrence of bleeding (all, major or minor) during the 12 week treatment interval

Secondary outcomes

  1. recurrent venous thromboembolism at 12 months

  2. death at 12 months

Sponsors and collaborators

Lead sponsor

University of Calgary

Other

Collaborators

  • Canadian Institutes of Health Research (CIHR)
  • Dupont Applied Biosciences
  • LEO Pharma

Registry information

Official study title

LITE Study, Appendix A (HOME-LITE), Amendment 6

Important dates

Study start
1997
Study completion
2000
First posted
Sep 20, 2005
Registry last updated
Feb 9, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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