Chronic Venous Insufficiency Clinical Trial
Official title:
Study of Antiinflammatory Effects of Detralex (Daflon) in Patients With Chronic Venous Disease
Verified date | October 2019 |
Source | University Hospital Dubrava |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Aim of the study:
To investigate if there is a differences in expression of inflammatory markers in venous wall
and blood among patients treated with Detralex and those not treated with Detralex (control
group).
Status | Completed |
Enrollment | 84 |
Est. completion date | September 2019 |
Est. primary completion date | May 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Chronic venous disease (CEAP 2 and 3) and saphenofemoral insufficiency Exclusion Criteria: - Previous deep venous thrombosis - Previous or acute thrombophlebitis of the GSV (confirmed by duplex findings - morphologic changes of the GSV above the knee) - Immunological disorders - Diabetes type I or II, - Severe inflammatory disease: such as Behcet, lupus, Horton and other arteritis, polyarthritis, spondylarthritis or sclerodermia - Recent (less than 3 months) or scheduled non-authorized non-pharmacological treatments: - Sclerotherapy, - Surgical treatment of varicose veins (crossectomy, phlebectomy), - Endovenous treatment (endovenous laser, radiofrequency), - Non-authorized pharmacological treatment in the last 3 months and during the study: - Anti-inflammatory agents (except acetylsalicylic acid at dose 350 mg daily), - Systemic corticosteroids or immunosuppressives, - Venoactive drugs including open label MPFF, - Pentoxifylline - Patients already (at the time of randomization) taking Detralex for symptoms linked to chronic venous disease - Arterial insufficiency (absent pedal pulses or ABI < 0.9) - Any important clinical or laboratory abnormalities - Pregnancy, breastfeeding or wish of becoming pregnant during the study |
Country | Name | City | State |
---|---|---|---|
Croatia | University Hospital Dubrava | Zagreb |
Lead Sponsor | Collaborator |
---|---|
University Hospital Dubrava | Servier |
Croatia,
Bergan JJ. Chronic venous insufficiency and the therapeutic effects of Daflon 500 mg. Angiology. 2005 Sep-Oct;56 Suppl 1:S21-4. Review. — View Citation
Eberhardt RT, Raffetto JD. Chronic venous insufficiency. Circulation. 2005 May 10;111(18):2398-409. Review. — View Citation
Nicolaides AN. From symptoms to leg edema: efficacy of Daflon 500 mg. Angiology. 2003 Jul-Aug;54 Suppl 1:S33-44. Review. — View Citation
Perrin M, Ramelet AA. Pharmacological treatment of primary chronic venous disease: rationale, results and unanswered questions. Eur J Vasc Endovasc Surg. 2011 Jan;41(1):117-25. doi: 10.1016/j.ejvs.2010.09.025. Epub 2010 Dec 3. Review. — View Citation
Sezer A, Usta U, Kocak Z, Yagci MA. The effect of a flavonoid fractions diosmin + hesperidin on radiation-induced acute proctitis in a rat model. J Cancer Res Ther. 2011 Apr-Jun;7(2):152-6. doi: 10.4103/0973-1482.82927. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Antiinflammatory Effects of Detralex (Daflon) | The following markers of inflammation will be analyzed: Blood (biochemical analysis): soluble ICAM-1, soluble VCAM-1, E-selectin, L selectin PAI-1, TIMP-1, Angiopoietin-1, Angiopoietin-2 and Tie-2. Vein wall ([immuno]histological and biochemical analysis) : CD 45 (leukocytes), S100 (C-fibers), MMP3, MMP9, SMC (smooth muscle cells). Presence (or not) of microthrombi in the vein lumen |
14 months | |
Secondary | Clinical effects of Detralex (Daflon) | Subjective perception of pain, leg heaviness, cramping and itching will be assessed using visual analogue scale (VAS) graded from 0 to 10. Leg edema will be assessed by measuring the leg circumference. Data will be recorded as follow: three months before the surgery one day before the surgery one week after the surgery one month after bthe surgery three months after the surgery |
14 months |
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