Evaluation of Pain Associated With the Removal of Wound Dressing During Care of Venous Leg Ulcer. Comparison of the Efficacy and Safety of Two Dressings Urgotul and TulleGras

Mylan

Status

Completed

Conditions

Venous Leg Ulcer

Treatments

Device: Urgotul

Device: TulleGras M.S.

Study type

Interventional

Funder types

Industry

Identifiers

NCT02104180

2013-A01285-40 (Other Identifier)

LINE4001

Details and patient eligibility

About

Evaluation of the non-inferiority of TulleGras M.S.® versus Urgotul® in pain associated with removal of wound dressing during care of venous leg ulcer

Enrollment

62 patients

Sex

All

Ages

45+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Subject informed of the objectives, purpose, details and constraints of the study and who has given his/her written informed consent.
Male or female subject.
Subject at least 45 years of age.
Subject presenting with an open venous leg ulcer.
Age of venous leg ulcer between 1 month and 12 months inclusive at the Inclusion Visit (Visit 1).
Venous leg ulcer whose area is between 4 cm2 and 50 cm2 inclusive at the Inclusion Visit (Visit 1).
Venous leg ulcer in the granulation phase over 50% of its area at the Inclusion Visit (Visit 1);

Exclusion criteria

Related to the disease studied:

Venous leg ulcer for which surgery is indicated or for which a surgical procedure is planned within twelve weeks of inclusion in the study (Visit 1).
Venous leg ulcer at start of cleaning phase;
Fibrinous and dry ulcer (non exudative wound) or on the contrary highly exudative and/or hemorrhagic.
Venous leg ulcer with signs of critical colonization or clinically infected.
Cancerous venous leg ulcer.

Related to the subject:

Subject presenting with a serious systemic disease, which may lead to premature termination of the study before the end of the twelve weeks of treatment of the Follow up Period.
Subject with a medical history or a significant disease revealed by history which can limit his/her participation or prevent the subject from completing the study.
Subject presenting with a progressive neoplasm, treated with radiotherapy or chemotherapy or immunosuppressant therapy or high-dose corticosteroids.
Subject who underwent surgery directly related to his/her venous disease during the two months prior to Inclusion Visit (Visit 1).
Subject with poorly controlled diabetes.
Subject who presented with a deep venous thrombosis during the 3 months prior to Inclusion Visit (Visit 1).
Subject confined to bed.
Woman of child-bearing potential (NOT postmenopausal for at least 24 months or NOT surgically sterilized (tubal ligation) or NOT hysterectomized) who is NOT routinely using adequate and efficient hormonal contraception or barrier method (intrauterine device, diaphragm, combination of condom and spermicide) prior to and during the trial.
Subject whose ankle has a circumference, measured at the Inclusion Visit (Visit 1), greater than 32 cm (> 32 cm).
Subject presenting with symptomatic or asymptomatic peripheral arterial disease, particularly with a distal systolic pressure index, measured at the Inclusion Visit (Visit 1), ≤0.8 or ≥1.3.
Subject with a history of allergic reaction(s) to one of the different components of the dressings or with a contra-indication to the use of one of these dressings.
Known history of alcohol abuse or drug abuse.
Subject linguistically or psychologically unable to understand the information given and to provide informed consent.
Subject participating in or who participated in another clinical study within 4 weeks prior to the Inclusion Visit (Visit 1).
Subject not covered by or not a beneficiary of the Social Security system.
Subject deprived of his freedom as the result of a legal or administrative decision or subject to legal guardianship.
Any other reason, in the investigator's opinion, that prohibits the inclusion of the subject into the study.