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INvestigating SIGnificant Health TrendS in the Management of Superficial Vein Thrombosis

INvestigating SIGnificant Health TrendS in the Management of Superficial Vein Thrombosis (INSIGHTS-SVT)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02699151
Acronym
INSIGHTS-SVT
Enrollment
1210
Registered
2016-03-04
Start date
2016-04-14
Completion date
2019-12-31
Last updated
2023-09-14

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

Conditions

Superficial Vein Thrombosis

Brief summary

Superficial vein thrombosis (SVT) and venous thromboembolism (VTE) are related entities. Only in the last years a series of observational studies mainly conducted in France could show that ´isolated SVT´ (without concomitant deep vein thrombosis and/or pulmonary embolism) is in fact not a benign and spontaneously healing disease but bears a potential for severe thromboembolic complications once not treated adequately. INSIGHTS-SVT study aims at collecting representative data on the current management and outcomes of SVT in Germany under real-life conditions. It will document the implementation of the recently issued national SVT guidelines issued by the Society for Angiology (DGA) and the Society for Phlebology (DGP).

Interventions

DRUGany drug

Any drug used for the treatment of SVT (e.g. heparin, low-molecular heparin, non-steroidal anti-inflammatory drug, fondaparinux, vitamin K antagonist)

PROCEDUREany procedure/surgery

Any procedure used for the treatment of SVT(e.g. sclerotherapy, endovenous thermotherapy, crossectomy, stripping, thrombectomy, phlebectomy)

OTHERAny non-pharmacological treatment of SVT

Any non-pharmacological treatment of SVT (including watchful waiting)

Sponsors

GWT-TUD GmbH
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Confirmed, acute, isolated SVT of the lower extremities * written informed consent

Exclusion criteria

* SVT located at ≤ 3 cm of the saphenofemoral crossing (as such patients need to be treated for DVT) * Subjects unlikely to comply with the requirements of the protocol (due to cognitive and/or language limitations) * Patient(likely) not available for 1-year documentation

Design outcomes

Primary

MeasureTime frameDescription
Efficacy: incidence of venous thromboembolism (VTE) events3 monthsVTE: composite of symptomatic pulmonary embolism (PE), symptomatic deep vein thrombosis (DVT), symptomatic recurrent superficial vein thrombosis (SVT), or symptomatic progression (extension) of SVT. This endpoint comprises symptomatic and asymptomatic VTE as reported by the treating physicians (usually diagnosed with compression ultrasonography or other appropriate methods). Events will be adjudicated.
Safety: incidence of major and clinically relevant bleeding events3 monthsDefinition of bleeding events is based on American College of Chest Physicians Evidence-Based Clinical Practice Guidelines (major bleedings) and the Comparison of Arixtra in lower limb superficial vein thrombosis with placebo (CALISTO) study definition (other bleedings), respectively. Events will be adjudicated.

Secondary

MeasureTime frameDescription
Incidence of superficial vein thrombosis (SVT)12 monthsSymptomatic recurrent SVT: new occurrence of symptomatic SVT confirmed by compression ultrasonography or duplex-ultrasonography, in any other superficial vein. Symptomatic progression of initially diagnosed SVT: extension by at least 2 cm, confirmed compression ultrasonography or duplex ultrasonography, and \> 3 cm away from the saphenofemoral crossing. Events will be adjudicated.
Death3 months and 12 months
New or recurrent cancer3 months and 12 months
VTE rates in the subgroup of patients who underwent surgical procedures for SVT3 months and 12 months
Predictors of VTE during follow-upthrough study completion, up to 12 months
Incidence of deep vein thrombosis (DVT)12 monthsSymptomatic and asymptomatic events as reported by the treating physician (usually diagnosed with compression ultrasonography or other appropriate methods). Events will be adjudicated.
Number of days in hospital due to VTEthrough study completion, up to 12 months
Number of days spent in rehabilitation due to VTEthrough study completion, up to 12 months
Numerical pain scalethrough study completion, up to 12 months0-10 point scale
Health-related quality of life on Euroquol 5 Dimensions questionnaire3 monthsEQ-5D questionnaire
Health related quality of life on VEnous Insufficiency Epidemiological and Economic Study questionnaire3 monthsVEINES-QOL/Sym questionnaire
Diagnostic procedures for venous thromboembolismthrough study completion, up to 12 monthsUtilisation rates of compression ultrasonography, duplex sonography, D-Dimer tests, computer tomography and other procedures typically used for the diagnosis of VTE.
Incidence of lung embolism (LE)12 monthsSymptomatic and asymptomatic events as reported by the treating physician. Events will be adjudicated.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026