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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03547921
Other study ID # sheba-18-4765-DS-CTIL
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date July 1, 2018
Est. completion date September 1, 2018

Study information

Verified date May 2018
Source Sheba Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of the study is to compare outcome of patients with effort thrombosis who were treated operatively to those treated nonoperatively


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 20
Est. completion date September 1, 2018
Est. primary completion date July 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:\

* patients treated for upper extremity DVT

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Device:
iu22 ultrasound system - phillips
iu22 ultrasound system - phillips

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Outcome

Type Measure Description Time frame Safety issue
Primary clinical differences clinical differences between the 2 groups Patients will be evaluated by the " Villata" post thrombotic syndrome (PTS) scoring system. The sum of each parameter will be used to compare he groups Vilata PTS scoring system: ( 0- ABSENT , 3 SEVERE ) Symptoms/clinical signs None Mild Moderate Severe Symptoms Pain Cramps Heaviness Pruritus Clinical signs edema Skin induration Hyperpigmentation Redness Venous ectasia Pain on calf compression 10years
Secondary vein patency patency of SCV based on duplex 10 years