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Completed

NCT Number: NCT00717938

A Study of Standard Treatment +/- Enoxaparin in Small Cell Lung Cancer

The endpoint is to investigate if the addition of low molecular heparin - enoxaparin, will result in a significant increase of overall survival in patients with small cell lung cancer, receiving standard chemotherapy.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Sahlgrenska University Hospital, Gothenburg, Sweden

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About this study

Chemotherapy will be given in accordance with local or regional guidelines but shall include a platinum drug + any topoisomerase inhibitor. Within these limits the study will accept different local variants as long as each centre remains consistent to its declared standard chemotherapy regimen. The recommended regimen is carboplatin or cisplatin plus etoposide q3 weeks for 4 cycles but up to 6 cycles is allowed. Local dosages and dose reduction schedules will be used.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histologically or cytologically verified SCLC, all stages
  • WHO performance status 0, 1, 2 or 3
  • Age 18 years or older
  • Intention and feasibility to treat with chemotherapy consisting of platinum + topoisomerase inhibitor.
  • Platelets >100 x109 /L
  • Signed informed consent
  • PK (prothrombin complex) INR and APTT within normal ranges.

Exclusion criteria

  • Prior systemic chemotherapy for lung cancer.
  • Concomitant anticoagulation treatment, except for ASA or clopidogrel
  • Active overt bleeding of clinical importance or at high risk (e.g. earlier observed haemorrhage in a brain metastasis, severe coagulopathy as haemophilia, severe liver dysfunction with impaired coagulation, acute peptic ulcer, and within the last 3 months suffered from intracranial haemorrhage, or surgery in the central nervous system).
  • Any other known contraindication for enoxaparine ( e.g. Hypersensitivity against enoxaparine and its derivatives).
  • Pregnancy or breast-feeding
  • Fertile women not using effective contraceptives or men who do not agree to use effective contraception during the treatment period.
  • Treatment with any other investigational agent, or participation in any other clinical trial.

Treatment and study plan

cisplatinum or carboplatin and e.g.etoposide.

Drug

Standard chemotherapy treatment for patients with small cell lung cancer. Chemotherapy regimen contains a platinum drug and a topoisomerase inhibitor. Numbers of cycles 4-6 according to local variants. Used drugs=cisplatinum or carboplatin and e.g.etoposide. Treatment will be given every three weeks for 4-6 cycles according to local variants.

Other names: cisplatinum, carboplatin, etoposide

cisplatinum or carboplatin and e.g.etoposide+enoxaparin

Drug

Standard chemotherapy treatment for patients with small cell lung cancer. Chemotherapy regimen contains a platinum drug and a topoisomerase inhibitor. Numbers of cycles 4-6 according to local variants. In addition to this, subjects will receive daily subcutaneous injections of enoxaparin during chemotherapy treatment.

Other names: cisplatinum, carboplatin, etoposide, enoxaparin

Primary outcomes

  1. Significant increase of overall survival

    Time frame: At follow up 1 year after treatment

Secondary outcomes

  1. Toxicity

    Time frame: During treatment

Sponsors and collaborators

Lead sponsor

Lund University Hospital

Other

Collaborators

  • Sanofi

Registry information

Official study title

A Randomized Phase III Study of Standard Treatment +/- Enoxaparin in Small Cell Lung Cancer

Acronym: RASTEN

Important dates

Study start
2008
Primary completion
2017
Study completion
2017
First posted
Jul 18, 2008
Registry last updated
Aug 25, 2017

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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