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Assessing effectiveness of topical gentamicin cream in junctional and dystrophic epidermolysis bullosa

Phase 2
Not yet recruiting
Conditions
Epidermolysis bullosa - Junctional and Dystrophic
Registration Number
CTRI/2018/08/015422
Lead Sponsor
PGIMER Chandigarh
Brief Summary

Epidermolysis bullosa (EB) comprises a group of heritable skin diseases characterized by fragile skin and mucous membranes and the formation of blisters in response to mechanical trauma or not. EB has a wide spectrum of phenotypes, ranging from mild features due to subtle molecular defects to severe cutaneous and extracutaneous manifestations due to severely compromised dermal-epidermal adhesion. Patients with EB need special care aimed at treating both the primary manifestations of the disease and their potential complications, which, in some cases, can be fatal.

As the areas of the body most often affected are sites subject to frequent pressure or friction, these conditions are also called mechanobullous disorders. The clinical complexity of this, as yet, incurable disease is further increased by extracutaneous manifestations, which include the involvement of skin adnexa, teeth, and the gastrointestinal, urinary tract, and pulmonary epithelia. There is presently no definitive cure for EB and the objective of treatment is to alleviate symptoms and provide supportive measures. Therapy is therefore focused on the prevention of lesions and complications.

Aminoglycosides are a class of antibacterials used mainly to treat Gram-negative bacterial infections Genetic and biochemical studies demonstrate that these antibiotics bind to the decoding site of ribosomal RNA of both and bring about a conformational change that permits codon–anticodon pairing during translation. Aminoglycosides reduce discrimination between cognate and near-cognate tRNA, permitting an amino acid to be inserted at the stop codon. The net effect is continuation of translation through to the natural stop codon expression and because of this it has been used in treatment of cystic fibrosis and ongoing trials on duchenne muscular dystrophy. In a recent study it has been seen to have similar effect in recesive dystrophic EB

In this study we plan to evaluate the efficacy of aminoglycosides in promoting wound healing and prevention of new blister formation in patients of EB. All the patients will be advised to apply topical gentamicin in a collagen base in one half of the body and paraffin guaze dressings on the other side for 12 weeks and the sides are reversed after 12 weeks. Clinical photography, physician global assessment will done monthly to evaluate ulcer healing and biopsy taken to evaluate the expression of proteins before and after treatment on both sides at 0, 12 and 24 weeks.  Paraffin guaze dressings side will act as control. Adequate precaution will be taken to monitor nephro and ototoxicity due to aminoglycosides by doing renal function tests weekly for 1 month and thereafter monthly and audiometry/BERA once every 2 months.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Inclusion criteria 1.
  • Patients with clinical diagnosis of EB and confirmed by IHC and/or molecular diagnosis 2.
  • Patients will be eligible for recruitment irrespective of gender.
  • Treatment naïve patients, which have not taken any treatment in the past six weeks and not on any systemic antibiotics.
Exclusion Criteria

Exclusion criteria: 1.Patients who have received any treatment in the past e.g. patients on topical/systemic antibiotics etc in the last 6 weeks 2.Patients with frank secondary bacterial infection or sepsis 3.Patients with infected wounds 4.Age <2 years.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
3.Number of days required for erosions to heal on right versus left sidePrimary Outcome | 1.Frequency of healed erosions on right versus left side | 2.Number of erosions on right versus left side | 3.Number of days required for erosions to heal on right versus left side | 4.To compare the clinical improvement in blister healing score with visual analogue score, physician global assessment and time taken to improve | 2. To evaluate decrease in appearance of new blisters over frequent trauma prone sites counted weekly for 24 weeks
Primary OutcomePrimary Outcome | 1.Frequency of healed erosions on right versus left side | 2.Number of erosions on right versus left side | 3.Number of days required for erosions to heal on right versus left side | 4.To compare the clinical improvement in blister healing score with visual analogue score, physician global assessment and time taken to improve | 2. To evaluate decrease in appearance of new blisters over frequent trauma prone sites counted weekly for 24 weeks
1.Frequency of healed erosions on right versus left sidePrimary Outcome | 1.Frequency of healed erosions on right versus left side | 2.Number of erosions on right versus left side | 3.Number of days required for erosions to heal on right versus left side | 4.To compare the clinical improvement in blister healing score with visual analogue score, physician global assessment and time taken to improve | 2. To evaluate decrease in appearance of new blisters over frequent trauma prone sites counted weekly for 24 weeks
2.Number of erosions on right versus left sidePrimary Outcome | 1.Frequency of healed erosions on right versus left side | 2.Number of erosions on right versus left side | 3.Number of days required for erosions to heal on right versus left side | 4.To compare the clinical improvement in blister healing score with visual analogue score, physician global assessment and time taken to improve | 2. To evaluate decrease in appearance of new blisters over frequent trauma prone sites counted weekly for 24 weeks
4.To compare the clinical improvement in blister healing score with visual analogue score, physician global assessment and time taken to improvePrimary Outcome | 1.Frequency of healed erosions on right versus left side | 2.Number of erosions on right versus left side | 3.Number of days required for erosions to heal on right versus left side | 4.To compare the clinical improvement in blister healing score with visual analogue score, physician global assessment and time taken to improve | 2. To evaluate decrease in appearance of new blisters over frequent trauma prone sites counted weekly for 24 weeks
2. To evaluate decrease in appearance of new blisters over frequent trauma prone sites counted weekly for 24 weeksPrimary Outcome | 1.Frequency of healed erosions on right versus left side | 2.Number of erosions on right versus left side | 3.Number of days required for erosions to heal on right versus left side | 4.To compare the clinical improvement in blister healing score with visual analogue score, physician global assessment and time taken to improve | 2. To evaluate decrease in appearance of new blisters over frequent trauma prone sites counted weekly for 24 weeks
Secondary Outcome Measures
NameTimeMethod
Secondary outcomes:1.To assess the change in expression of proteins using IF positivity before and after treatment in right versus left side

Trial Locations

Locations (1)

PGIMER Chandigarh

🇮🇳

Chandigarh, CHANDIGARH, India

PGIMER Chandigarh
🇮🇳Chandigarh, CHANDIGARH, India
Dr Rahul Mahajan
Principal investigator
1722756562
drrahulpgi@yahoo.com

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