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

Primary Purpose

Epidermolysis Bullosa

Status
Unknown status
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Oral erythromycin
Sponsored by
Centre Hospitalier Universitaire de Nice
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Epidermolysis Bullosa

Eligibility Criteria

6 Months - 8 Years (Child)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • CHU de DijonRecruiting
  • Hôpital Saint Eloi
  • CHU de Nice - Hôpital de CimiezRecruiting
  • Hôpital PurpanRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Oral erythromycin

Arm Description

Oral erythromycin

Outcomes

Primary Outcome Measures

number of patients with decrease of blisters' number of at least 20% after 3 months of treatment by oral erythromycin
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

Secondary Outcome Measures

Secondary end points are : effect of 3 months of oral erythromycin on - Global tolerance of treatment.
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
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,
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.

Full Information

First Posted
April 11, 2011
Last Updated
October 13, 2011
Sponsor
Centre Hospitalier Universitaire de Nice
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1. Study Identification

Unique Protocol Identification Number
NCT01340235
Brief Title
Treatment of Dowling Maera Type of Epidermolysis Bullosa Simplex by Oral Erythromycin
Official Title
Treatment of Dowling Maera Type of Epidermolysis Bullosa Simplex by Oral Erythromycin
Study Type
Interventional

2. Study Status

Record Verification Date
October 2011
Overall Recruitment Status
Unknown status
Study Start Date
June 2011 (undefined)
Primary Completion Date
December 2011 (Anticipated)
Study Completion Date
June 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centre Hospitalier Universitaire de Nice

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epidermolysis Bullosa

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Oral erythromycin
Arm Type
Experimental
Arm Description
Oral erythromycin
Intervention Type
Drug
Intervention Name(s)
Oral erythromycin
Intervention Description
Severe Dowling Meara EBS patients from 6 months to 8 years old
Primary Outcome Measure Information:
Title
number of patients with decrease of blisters' number of at least 20% after 3 months of treatment by oral erythromycin
Description
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
Time Frame
at 3 months of treatment
Secondary Outcome Measure Information:
Title
Secondary end points are : effect of 3 months of oral erythromycin on - Global tolerance of treatment.
Description
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.
Time Frame
at 3 months of treatment
Title
Secondary end points are : effect of 3 months of oral erythromycin on - Involved area
Description
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.
Time Frame
at 3 months of treatment
Title
Secondary end points are : effect of 3 months of oral erythromycin on - pruritus,
Description
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.
Time Frame
at 3 months of treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christine Chiaverini, PH
Organizational Affiliation
Centre Hospitalier Universitaire de Nice
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Dijon
City
Dijon
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierre Vabres, PU-PH
Email
pierre.vabres@chu-dijon.fr
Facility Name
Hôpital Saint Eloi
City
Montpellier
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Didier Bessis, PH
Facility Name
CHU de Nice - Hôpital de Cimiez
City
Nice
ZIP/Postal Code
06000
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Christine Chiaverini, PH
Phone
0033 4 92 03 61 07
Email
chiaverini.c@chu-nice.fr
First Name & Middle Initial & Last Name & Degree
Vanina Oliveri, ARC
Phone
0033 4 92 03 42 54
Email
oliveri.v@chu-nice.fr
Facility Name
Hôpital Purpan
City
Toulouse
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juliette MAZEREEUW, PU-PH
Phone
00 33 5 67 77 81 41
Email
mazereeuw-hautier.j@chu-toulouse.fr

12. IPD Sharing Statement

Learn more about this trial

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

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