Efficacy and Safety of Diosmin 600mg Versus Placebo on Painful Symptomatology in Patients With Chronic Venous Disease of Lower Limbs (EDEN)

Assessment of the Efficacy and Safety of Diosmin 600mg on Painful Symptomatology in Patients With Chronic Venous Disease of Lower Limbs: a Multicentric, Randomised, Double-blind, Placebo-controlled Trial in Parallel Groups

Diosmin has a well established use status in improvement of the symptoms of venolymphatic insufficiency: heavy legs, pain, primo-decubitus restlessness and as complement treatment of capillary fragility.

Nevertheless, diosmin 600 mg did not benefit from a rigorous clinical study versus placebo, to establish its efficacy in the pain relief in Chronic Venous Disease (CVD).

The aim of this project led by Dr. Guex is to evaluate the efficacy and safety of diosmin 600 mg - DIOVENOR® on the painful symptoms of CVD of the lower limbs, in a multicentre, controlled, randomised, double blind, placebo-controlled, parallel-group study.

Study Overview

• Status: Completed
• Conditions: Chronic Venous Disease of Lower Limbs
• Intervention / Treatment: Drug: Diosmin; Drug: Placebo

• Study Type: Interventional
• Enrollment (Actual): 378
• Phase: Phase 3

Contacts and Locations

Study Locations

• France
  • Nice, France, 06000
    • Dr Jean-Jérôme GUEX

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Patient, man or woman, aged 18 and over,
2. Patient presenting a C1s or C2s venous disease grade of the lower limbs
3. Patient presenting a painful venous symptomatology in the lower limbs for at least 15 days.
4. Patient suffering from venous symptomatology in one leg with a painful symptom intensity higher or equal to 30 mm (VAS= 100mm)

Exclusion Criteria:

1. Patient treated by venotonic treatments or vascular protectants or assimilated dietary supplements or homeopathic treatments or diuretics within 15 days prior inclusion,
2. Patients who started treatments such as calcium inhibitors, beta-blockers, angiotensin converting enzyme inhibitors and/or vasodilators and/or vasoconstrictors within 28 days prior inclusion (for patients already taking this type of treatments, dosage should not have been changed in the 28 days prior inclusion and should not be planned to change in the course of the study),
3. Patient treated by any analgesic within 7 days prior inclusion,
4. Patient treated by an anti-inflammatory treatment within 7 days prior inclusion,
5. Patient using elastic venous compression
6. Patient presenting permanent oedema,
7. Patients presenting venous skin changes,
8. Patient whose activity in the 4 following weeks (that is to say during the study) would be different from his/her usual activities (before the study),
9. Patient suffering from a pathology generating other pains than venous pains in the lower limbs,
10. Patient with a history of lower limbs trauma responsible for sequel pains,
11. Patient with a known deep venous reflux,
12. Patient with a history of venous thromboses or thrombo-embolic diseases within the last 6 months before inclusion,
13. Patient treated with analgesics or anti-inflammatory treatments used as analgesics within 4 weeks prior inclusion
14. Patient having a known hypersensitivity to diosmin or one of the excipients
15. Patients with rare hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption ),

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Placebo Comparator: Placebo	Drug: Placebo; tablet, PO, 1 per day during 28 days
Experimental: Diosmin	Drug: Diosmin; tablet, 600mg, PO, 1 tab per day during 28 days

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Change of Visual analog Scale score for assessment of the painful venous symptomatology	baseline and after 28 days

Secondary Outcome Measures

Outcome Measure	Time Frame
- Painful symptom intensity (daily VAS score) Area Under the Curve	28 days
- Daily VAS score for Response rate	28 days
- Daily VAS score for Time to response	28 days
- Score of Quality of life questionnaire (SQOR-V)	Between baseline and 28 days
- Patient's and physician's global satisfaction score	At 28 days
Adverse Events (numbers and frequency)	28 days
- Unusual intakes of analgesic treatments (rate of patients)	28 days

Collaborators and Investigators

• Sponsor: Laboratoire Innotech International
• Investigators: Principal Investigator: Jean-Jérôme GUEX, MD

Publications and helpful links

General Publications

• Martinez-Zapata MJ, Vernooij RW, Simancas-Racines D, Uriona Tuma SM, Stein AT, Moreno Carriles RMM, Vargas E, Bonfill Cosp X. Phlebotonics for venous insufficiency. Cochrane Database Syst Rev. 2020 Nov 3;11(11):CD003229. doi: 10.1002/14651858.CD003229.pub4.

Study record dates

Study Major Dates

• Study Start: January 1, 2012
• Primary Completion (Actual): March 1, 2013
• Study Completion (Actual): April 1, 2013

Study Registration Dates

• First Submitted: February 10, 2012
• First Submitted That Met QC Criteria: February 14, 2012
• First Posted (Estimate): February 15, 2012

Study Record Updates

• Last Update Posted (Estimate): April 29, 2013
• Last Update Submitted That Met QC Criteria: April 26, 2013
• Last Verified: April 1, 2013

More Information

Terms related to this study

• Other Study ID Numbers: DIO401-10