Treatment of Dowling Maera Type of Epidermolysis Bullosa Simplex by Oral Erythromycin

This study is currently recruiting participants.
Verified October 2011 by Centre Hospitalier Universitaire de Nice
Sponsor:
Information provided by (Responsible Party):
Del Cont Delphine, Centre Hospitalier Universitaire de Nice
ClinicalTrials.gov Identifier:
NCT01340235
First received: April 11, 2011
Last updated: October 13, 2011
Last verified: October 2011

April 11, 2011
October 13, 2011
June 2011
December 2011   (final data collection date for primary outcome measure)
number of patients with decrease of blisters' number of at least 20% after 3 months of treatment by oral erythromycin [ Time Frame: at 3 months of treatment ] [ Designated as safety issue: Yes ]
Principal end point is evaluated at inclusion and after one month of treatment, 3 months of treatment and 2 months after the end of the treatment
Same as current
Complete list of historical versions of study NCT01340235 on ClinicalTrials.gov Archive Site
  • Secondary end points are : effect of 3 months of oral erythromycin on - Global tolerance of treatment. [ Time Frame: at 3 months of treatment ] [ Designated as safety issue: Yes ]
    For each patient and globally, the nature, the frequency and the severity of the various unwanted effects will be described on the duration of the study.
  • Secondary end points are : effect of 3 months of oral erythromycin on - Involved area [ Time Frame: at 3 months of treatment ] [ Designated as safety issue: Yes ]
    These criteria will be analyzed in comparison with the values to the inclusion (M0). We shall try to estimate the obstinacy of an effect 2 months after the end of the treatment.
  • Secondary end points are : effect of 3 months of oral erythromycin on - pruritus, [ Time Frame: at 3 months of treatment ] [ Designated as safety issue: Yes ]
    These criteria will be analyzed in comparison with the values to the inclusion (M0). We shall try to estimate the obstinacy of an effect 2 months after the end of the treatment.
Same as current
Not Provided
Not Provided
 
Treatment of Dowling Maera Type of Epidermolysis Bullosa Simplex by Oral Erythromycin
Treatment of Dowling Maera Type of Epidermolysis Bullosa Simplex by Oral Erythromycin

Dowling Meara type of epidermolysis bullosa simplex (EBS-DM) is a rare genodermatosis due to keratin 5 and 14 mutation, characterized by skin fragility and spontaneous or post traumatic blisters. Neonatal period and infancy are critical since this autonomic dominant affection usually improves with age. Cyclins seem to be efficient in some cases of EBS but are prohibited in children younger than 8 years old. Erythromycin can be a good alternative in this population due to its antibacterial and anti-inflammatory potential.

The aim of this study is the evaluation of the efficiency of oral erythromycin to decrease the number of cutaneous blisters in severe EBS-DM patients from 6 months to 8 years old after 3 months of treatment.

Primary end point is the number of patients with decrease of blisters' number of at least 20% after 3 months of treatment by oral erythromycin.

It is a preliminary study on 8 patients. Treatment is oral erythromycin twice a day during 3 months. Follow up for each patient is 5 months. The duration of the study is 1 year.

Not Provided
Interventional
Phase 3
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Epidermolysis Bullosa
Drug: Oral erythromycin
Severe Dowling Meara EBS patients from 6 months to 8 years old
Experimental: Oral erythromycin
Oral erythromycin
Intervention: Drug: Oral erythromycin
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
8
June 2012
December 2011   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Severe Dowling Meara EBS patients (2 or more new blisters a day)
  • signature of informed consent
  • Patient of 2 sexes
  • Age from 6 months to 8 years. From this age we consider that the patient will less need this treatment or can take cyclines.
  • Systematic Obtaining of the consent lit(enlightened) by the relatives(parents) of the child, after information about the objectives and the constraints of the study.
  • Agreement of the minor
  • Patient member to the Social Security

Exclusion Criteria:

  • Patient allergic to the erythromycin
  • Patient presenting an intolerance to the fructose, a syndrome of malabsorption some glucose and some galactose or a deficit sucrase-isomaltase
  • Renal and\or hepatic Insufficiency
  • Patient taking a medicine against indicated or misadvised in association with the erythromycin
Both
6 Months to 8 Years
No
Not Provided
France
 
NCT01340235
10-PP-19
No
Del Cont Delphine, Centre Hospitalier Universitaire de Nice
Centre Hospitalier Universitaire de Nice
Not Provided
Principal Investigator: Christine Chiaverini, PH CHU de NIce
Centre Hospitalier Universitaire de Nice
October 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP