Skip to content

Prospective Evaluation of the Treatment of Cancer Associated Superficial Venous

Prospective Evaluation of the Treatment of Cancer Associated Superficial Venous

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07210671
Acronym
SUPERCAT
Enrollment
1576
Registered
2025-10-07
Start date
2025-11-10
Completion date
2028-11-01
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer, Superficial Vein Thrombosis, Venous Thrombosis

Keywords

Superficial vein thrombosis, cancer, venous thrombosis

Brief summary

Superficial venous thrombosis (SVT) is very common in clinical practice. What's more, around 15- 20% of SVTs occur in the context of cancer. Today, cancer patients are excluded from therapeutic trials for DVT. There is therefore no high-level evidence-based treatment recommendation for these patients. Recent data suggest that the course of cancer-associated DVT is similar to that of cancer-associated deep vein thrombosis (DVT). However, there are currently few prospective data on the evolution of cancer-associated DVT in relation to the treatment used. Due to the absence of clear recommendations of treatment in case of SVT associated with cancer the investigators will perform a prospective observational study to evaluate the efficacy of different regiment of anticoagulant treatment ordered in clinical practice.

Interventions

None listed

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient over 18 * Patient affiliated to a social security scheme * Patient who understands French * Patient with superficial venous thrombosis of the lower and upper limbs confirmed by a Doppler ultrasound less than one month old. * Patient with active cancer: * Cancer treatment within the last 6 months, * Detectable tumor disease, cancer treatment within the last 6 months, ongoing hormone therapy for cancer, palliative cancer. * The patient has received potentially non-curative cancer treatment (notably palliative chemotherapy). * Progression shows that the cancer treatment was not curative (due to recurrence or progression under treatment) (particularly in the case of recurrence after surgery)

Exclusion criteria

* Patients under legal protection * Patients with concomitant pulmonary embolism * Patient with proximal or distal deep vein thrombosis * Patient treated with anticoagulant therapy for another indication * Patient with a contraindication to anticoagulation: Thrombocytopenia less than 30,000 elements/mm3, active bleeding or history of severe bleeding. * Patient opposed to participation in research

Design outcomes

Primary

MeasureTime frameDescription
risk (in %) of recurrence of VTEat 3-month follow-uprisk of recurrence of VTE at 3-month follow-up in patients with cancer-associated SVT.

Secondary

MeasureTime frame
association (%) between initial treatment and the risk of SVT recurrenceat 3 months
Association (%) between initial treatment and the occurrence of pulmonary embolism (PE)at 12 months
Association (%) between initial treatment and the occurrence of DVTat 3 months
association (%) between initial treatment and bleeding eventsat 6 months
association(%) between initial treatment and all-cause deathat 3 months
rates of recurrence of symptomatic vs. incidental VTEat 3 months
rate of confirmed cancer in patients with TVS suspected of having cancer.at 12 months

Countries

France

Contacts

CONTACTSimon SOUDET, Dr
soudet.simon@chu-amiens.fr33+3 22 08 80 51

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 15, 2026