Actively Recruiting

Phase Not Applicable
Age: 15Years +
All Genders
NCT05979506

Evaluate the Evolution of Body and Scalp Skin Discomfort in Patients With Hereditary Ichthyosis After Wraps (EnvelopIchtyose)

Led by University Hospital, Toulouse · Updated on 2026-04-13

34

Participants Needed

1

Research Sites

140 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Ichthyosis is a group of rare and chronic genetic diseases beginning at birth, in which the patient's skin is covered with scales of variable appearance and severity. This disease is disabling. The treatment is symptomatic and is based on the daily application of moisturizing creams with a high lipid content. Nevertheless, the effectiveness of these treatments is limited and are considered very painful by the patients. Wraps are local treatments carried out by specialized nurses and which consist in, following a therapeutic bath, applying a large quantity of cream to the whole body, followed by an occlusion. This type of care is simple to perform, but requires nursing expertise, to date, it is not carried out in standard practice in France, which is why the investigateur wish to evaluate the effect of wraps on different parameters reflecting the skin condition in the short and medium term.

CONDITIONS

Official Title

Evaluate the Evolution of Body and Scalp Skin Discomfort in Patients With Hereditary Ichthyosis After Wraps (EnvelopIchtyose)

Who Can Participate

Age: 15Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient with hereditary ichthyosis regardless of the clinical form
  • Patient with a scaling or erythema score > 6/16
  • Patient with a skin discomfort score > 3/10
  • Patient having given written, free and informed consent
  • Patient affiliated to a social security scheme
Not Eligible

You will not qualify if you...

  • Patient with a skin disease other than ichthyosis
  • Patient having modified his treatments for ichthyosis in the month preceding inclusion
  • Patient with known intolerance or allergy to one of the topicals used in the study
  • Patient unable to complete the study questionnaires
  • Patient under a protection regime

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Toulouse University hospital

Toulouse, France, 31059

Actively Recruiting

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Research Team

A

Anne-Marie TRANIER

CONTACT

R

RASMUS Lysa

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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