Clinical trial · Interventional
Anticoagulation and Inferior Vena Cava Filters in Cancer Patients With a Venous Thromboembolism
A Randomized Control Trial of Anticoagulation and Inferior Vena Cava Filters in Cancer Patients With A Venous Thromboembolism
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Study accrual stopped due to poor accrual.
Summary
Brief summary (as posted)
The development of clots is a potentially deadly complication in many cancer patients. The current optimal treatment is unknown. Evidence supporting the effectiveness of the use of Inferior Vena Caval Filters is lacking. This study will compare the two standard of care treatment options: anticoagulation with or without a inferior vena cava filter. The anticoagulation medication chosen will be Arixtra and it will be given once a day as an injection. Patients will be called at various intervals to monitor their signs and symptoms of new thromboembolisms.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
| Thromboembolism | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Arixtra alone | Drug | — | UNRESOLVED |
| Arixtra + filter | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- 1- Arixtra Alone
- description
- Arixtra Alone
- interventionNames
- Drug: Arixtra alone
- type
- ACTIVE_COMPARATOR
- label
- 2 Arixtra+ filter
- description
- Arixtra + filter
- interventionNames
- Device: Arixtra + filter
Primary outcomes (1)
- measure
- Adverse Outcomes
- timeFrame
- 3 years or until death
- description
- Rates of VCF complications, bleeding, and recurrent or residual DVTs or PEs
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Documentation of cancer. * The disease may be a solid tumor, Lymphoma or Multiple Myeloma. Pathology reports will be documented in the patient's chart and included in the data. * Age \> 18 years * An acute, radiographically confirmed, de novo Deep Vein Thrombosis (DVT) or Pulmonary Embolism (PE) * No past medical history of a prior thrombus or known thrombophilia Exclusion Criteria * Patients are not eligible for this study if they receive therapeutic doses of any heparin for more than 72 hours before randomization 31. * Already receiving oral anticoagulant therapy 31. * Severe renal impairment, calculated using the Cockcroft-Gault formula, defined as a creatinine clearance \<30 mL/min 31. * Platelet count of less than 50,000 per cubic millimeter * Bleeding from the gastrointestinal tract that requires blood transfusion (s), intracranial bleeding or retroperitoneal bleeding. * An indication for thrombolysis * Allergy to iodine * Hereditary thrombophilia * Pregnancy * Likelihood of noncompliance * It is contraindicated to anticoagulate patients with brain metastasis secondary to melanoma, choriocarcinoma, renal cell and medullary thyroid carcinoma. If these patients have a Venous Thromboembolism (VTE), it is standard of care for these patients to have a CT of their head to evaluate if there is metastasis to the brain before they are anticoagulated 38. If these patients do have brain metastasis, they will not be included in the study.
References
Publications (0)
Data not yet available