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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01501175
Other study ID # 1108036
Secondary ID 11.385
Status Completed
Phase N/A
First received December 27, 2011
Last updated February 12, 2013
Start date November 2011
Est. completion date January 2013

Study information

Verified date February 2013
Source Centre Hospitalier Universitaire de Saint Etienne
Contact n/a
Is FDA regulated No
Health authority France: French Data Protection Authority
Study type Observational

Clinical Trial Summary

To date, the investigators still do not know the annual incidence of Superficial Vein Thrombosis in the legs, although the investigators do know that this pathology is frequent and the investigators can assume its incidence is greater than Deep Vein Thrombosis which is of 1 to 2 cases per year per 1,000 inhabitants. Furthermore, the high percentage of SVT with concomitant DVT and Pulmonary Embolism only concerns patients seen in vascular medicine, so it is important to re-evaluate this rate on an unselected population from general practice.


Description:

The method is a prospective observational study involving all the general practitioners and vascular physicians of the Saint Etienne region, i.e. 276 general practitioners, 27 vascular physicians and 341,822 inhabitants. Any new case of symptomatic SVT in the legs suspected by the general practitioner and confirmed by compression ultrasonography by the vascular physician would be listed over one year. The confirmed SVTs, directly seen by the vascular physicians would also be listed. The incidence would be calculated by relating the total number of SVTs observed to the number of inhabitants of the Saint Etienne region. Information on whether concomitant DVT exists or not at the time of the compression ultrasonography would also be collected.


Recruitment information / eligibility

Status Completed
Enrollment 848
Est. completion date January 2013
Est. primary completion date November 2012
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- inhabitants of the Saint Etienne region

- with suspected SVT

- consulting general practitioners and or vascular physicians of the Saint Etienne region

Exclusion Criteria:

- SVT not confirmed by compression ultrasonography

Study Design

Observational Model: Case-Only, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Intervention

Other:
consultation with a vascular physician
As in usual practice, patient with suspected SVT will consult a vascular physician to diagnose SVT and eventually DVP/PE associated. Vascular physician will collect risk factors of SVT.

Locations

Country Name City State
France Cabinet D'Angiologie Firminy
France Ch Firminy Firminy
France Cabinet D'Angiologie Saint Chamond
France Cabinet D'Angiologie Saint Etienne
France Centre médical de Chavannes Saint-chamond
France Cabinet D'Angiologie Saint-etienne
France Chu Saint-Etienne Saint-etienne
France Clinique Mutualiste CHirurgicale de St-Etienne Saint-etienne

Sponsors (2)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne Ministry of Health, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary symptomatic SVT new case of symptomatic SVT in the legs suspected by the general practitioner and confirmed by compression ultrasonography by the vascular physician 1 year No
Secondary SVT risk factors SVT risk factors will be collected during consultation with vascular physician. They are: varicose veins, history of thromboembolism, autoimmune disease,cancer, immobilization, recent surgery 1 year No
Secondary SVT Clinical signs SVT clinical signs will be collected during consultation with general practitioner and or vascular physician. They are: palpable cords, pain, erythematous area and surrounding edema. 1 year No
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