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NCT01110512

Comparative Efficacy of Two Preparations of the Association Diosmin (450 mg) + Hesperidin (50 mg) in the Treatment of Chronic Venous Insufficiency (CVI)

Status unknown Phase 3 Last updated 26 October 2010
What this trial tests

Phase 3 trial testing Flavonid in Venous Insufficiency in 140 participants. Status unknown.

Timeline
1 October 2010
Primary endpoint
1 December 2010
1 March 2011

Quick facts

Lead sponsorAzidus Brasil
PhasePhase 3
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment140
Start date1 October 2010
Primary completion1 December 2010
Estimated completion1 March 2011
Sites1 location across Brazil

Drugs / interventions tested

Conditions studied

Sponsor

Azidus Brasil — full company profile →

Who can join

Adults 18 to 75, any sex, with Venous Insufficiency. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

It is hoped that with the use of medication, occurs improvement of the CVI parameters, such as edema, pain, night cramps, functional discomfort, heavy feeling and that the drug test is non-inferior than the comparator.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Venous Insufficiency

Currently open trials in the same condition.

Other Azidus Brasil trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01110512.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing