Safety And Efficacy Study Of Topic Mucopolysaccharide Polysulfate In The Superficial Varicose Veins Treatment

Last updated: February 23, 2021
Sponsor: EMS
Overall Status: Trial Not Available

Phase

3

Condition

Occlusions

Vascular Diseases

Varicose Veins

Treatment

N/A

Clinical Study ID

NCT01203397
MPSEMS0110
  • Ages 18-80
  • All Genders

Study Summary

Evaluate the safety, tolerability and effectiveness of mucopolysaccharide polysulfate in the treatment of superficial varicose veins

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients must be able to understand the study procedures, agree to participate, andgive written consent.
  • Patients must be able to follow the study medication regimen.
  • Patients with inflammatory process in superficial veins for more than 72 hours.
  • Presence of symmetric lesions to compare one side to the other.

Exclusion

Exclusion Criteria:

  • Pregnancy or risk of pregnancy.
  • Lactation.
  • Use of topical or systemic anti-inflammatory, antihistamine or immunosuppressive drugswithin the last 48 hours prior to the study
  • Any alteration at other deep veins.
  • History of atopy or allergic diseases.
  • History of allergy to any component of the formulations.
  • Other conditions considered by the investigator as reasonable for non-eligibility.

Study Design

Study Start date:
September 01, 2014
Estimated Completion Date:
February 28, 2015

Connect with a study center

  • Medcin Instituto Da Pele

    Osasco, SÃO Paulo 060323-000
    Brazil

    Site Not Available

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