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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00303407
Other study ID # SPOT 99/54
Secondary ID
Status Terminated
Phase Phase 4
First received March 15, 2006
Last updated March 15, 2006
Start date January 2001
Est. completion date July 2002

Study information

Verified date December 2005
Source University Hospital, Geneva
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

To determine the efficacy and to measure the complications of prophylactic anticoagulation using low-molecular weight heparin in adult cancer patients under palliative care


Recruitment information / eligibility

Status Terminated
Enrollment 0
Est. completion date July 2002
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Cancer patients in palliative care

- Patients fully informed about their condition

- Signed informed consent

- No exclusion criteria

Exclusion Criteria:

- Absence of advanced cancer

- Cancer previously cured

- Venous thromboembolism diagnosed within 6 months prior to inclusion

- Absence of discerning capacity

- Active anti-thrombotic treatment with heparins or coumarines

- Thrombocytopenia <50G/l

- PTT >45sec

- TP<35%

- Active bleeding

- Renal failure <20ml/min

- Past history of heparin-induced thrombocytopenia

Study Design

Observational Model: Defined Population, Time Perspective: Longitudinal


Related Conditions & MeSH terms


Intervention

Drug:
nadroparin


Locations

Country Name City State
Switzerland Center of Continuous Care, chemin de la Savonnière Collonge-Bellerive (Geneva) Geneva

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Geneva

Country where clinical trial is conducted

Switzerland, 

References & Publications (1)

Prandoni P. Antithrombotic strategies in patients with cancer. Thromb Haemost. 1997 Jul;78(1):141-4. Review. — View Citation

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