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RecruitingNCT05979506Updated Apr 13, 2026

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

An interventional study of Cutaneous wraps in Ichthyosis Inherited, sponsored by University Hospital, Toulouse. Recruiting at 1 site in France. Open to participants aged 15 Years and older. Per ClinicalTrials.gov, last updated 2026-04-13.

Sponsored by University Hospital, Toulouse · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Feb 2024; still recruiting 2 years 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
34
Allocation
Not applicable
Ages
15 Years and older
Sex
All
01

Study summary

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.

Read the detailed description

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. There are 2 distinct typical profiles: patients with thick scales without erythroderma and patients with finer scales on an erythrodermic background. This disease is disabling, in particular due to sensations of pruritus, skin pain and the possible presence of associated extra-cutaneous abnormalities. The treatment is symptomatic and is based on the daily application of moisturizing creams with a high lipid content for better effectiveness, keratolytic creams, and for severe forms, oral retinoids may be necessary. The creams improve the condition of the skin and reduce the sensations of skin discomfort, pain and pruritus, 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. The type of cream is adapted to the area of application: thus, an emollient cream is used for the body; a cream enriched with keratolytic active ingredients is used for the feet in the event of hyperkeratosis, and an emollient cream possibly enriched with keratolytic active ingredients is used for the scalp, followed by an exposure time under a steam helmet to remove scales. This type of care is simple to perform, but requires nursing expertise, to date, it is not carried out in standard practice in France, except in the centers of Toulouse, Bordeaux and Necker and at the thermal cure of Avène-les-Bains. However, the interest of such a treatment has never been evaluated independently, which is why in this study the investigators want to evaluate the effect of carrying out a daily treatment over 3 consecutive days, on different parameters reflecting the skin condition in the short and medium term

02

Conditions studied

  • Ichthyosis Inherited

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Keywords

  • Ichthyosis
  • inherited
  • wraps
  • skin scales
  • cutaneous abnormalities
03

In context

Ichthyosis

33 studies on the registry are indexed under Ichthyosis; 11 are open to participants now.

This study's planned enrollment of 34 is above the median of 26 across 23 interventional studies indexed under Ichthyosis.

Browse Ichthyosis studies →

Lead sponsor

University Hospital, Toulouse is the lead sponsor of 807 studies on the registry; 209 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
15 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • 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
  • Patient affiliated to a social security scheme

Exclusion criteria

Exclusion Criteria:

  • 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
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
34 participants (estimated)

Study arms

  • Experimental
    Wraps (body and feet) as well as scalp care

    The skin care consisting of wraps (body and feet) and scalp care, will be carried out consecutively over 3 days, in the hospital (outpatient or in day/traditional hospitalization).

    Procedure: Cutaneous wraps

Interventions

  • ProcedureCutaneous wraps

    The topical treatment that will be used in this study are: * For the body, an emollient cream with a high lipid content: Cold cream * For the scalp and feet, an emollient preparation with keratolytic action: 10% or 30% urea, depending on the scalp and feet damage Each of the 3 treatments (body, scalp and feet) will be carried out as follows: * Application of different topicals all over the body and face, after taking a lukewarm therapeutic bath of 20 minutes * Occlusion by "wrapping" the patient in a plastic film, then covering with a blanket * After 1 hour, the unabsorbed excess cream is removed with a towel

06

What researchers measure

Primary outcomes

  1. Skin discomfort Analogue Visual Scale (AVS)

    Percentage of patients showing a reduction of at least 3 points of their skin discomfort in the entire body, measured with the AVS scale (0-10) of cutaneous discomfort between baseline and 11 days after treatment

    Time frame: day 11

Secondary outcomes

  1. Reduction of skin discomfort - day 4

    Percentage of patients showing a reduction of at least 3 points of their skin discomfort in the entire body, measured with the Analogue Visual Scale (AVS) (0-10) of cutaneous discomfort between baseline and day 4

    Time frame: day 4

  2. Reduction of skin discomfort - day 30

    Percentage of patients showing a reduction of at least 3 points of their skin discomfort in the entire body, measured with the Analogue Visual Scale (AVS) (0-10) of cutaneous discomfort between baseline and day 30

    Time frame: day 30

  3. Variation of erythema and scales severity - Visual Index for Ichthyosis Severity

    Variation of erythema and scales severity judged by : \- Their intensity, measured with the Visual Index for Ichthyosis Severity (VIIS) : scores scored separately out of 16. The 16 point scorring is : 4 zones: upper back, upper arm, lower legs, top of foot, scored out of 4 with 0 = no lesions, 1 = areas of normal skin with small scales, 2 = confluent smoothing, 3 = confluent scales and 4 = confluent scale

    Time frame: day 4

  4. Variation of erythema and scales severity

    Variation of erythema and scales severity judged by : -Their extent, measured with the scores A and B of the Specific Clinical Ichthyosis Score

    Time frame: day 4

  5. Cutaneous pain - day 4

    Variation of pain assessed by the Analogue Visual Scale (0-10) of skin pain

    Time frame: day 4

  6. pruritus - day 4

    Variation of pruritus assessed by the Analogue Visual Scale (0-10)

    Time frame: day 4

  7. sweating - day 4

    Variation of sweating assessed by the Analogue Visual Scale (0-10)

    Time frame: day 4

  8. Cutaneous pain - day 11

    Variation of pain assessed by the Analogue Visual scale (0-10) of skin pain

    Time frame: day 11

  9. pruritus - day 11

    Variation of pruritus assessed by the Analogue Visual scale (0-10)

    Time frame: day 11

  10. sweating - day 11

    Variation of sweating assessed by the Analogue Visual Scale scale (0-10)

    Time frame: day 11

  11. Cutaneous pain - day 30

    Variation of pain assessed by the Analogue Visual Scale (0-10) of skin pain

    Time frame: day 30

  12. pruritus - day 30

    Variation of pruritus assessed by the Analogue Visual Scale scale (0-10)

    Time frame: day 30

  13. sweating - day 30

    Variation of sweating assessed by the Analogue Visual Scale (0-10)

    Time frame: day 30

  14. Feet and scalp discomfort - day 4

    Percentage of patients showing a reduction of at least 3 points of their skin discomfort in the feet and scalp, measured with the Analogue Visual Scale (0-10) of cutaneous discomfort

    Time frame: day 4

  15. Feet and scalp discomfort - day 11

    Percentage of patients showing a reduction of at least 3 points of their skin discomfort in the feet and scalp, measured with the Analogue Visual Scale (0-10) of cutaneous discomfort

    Time frame: day 11

  16. Feet and scalp discomfort - day 30

    Percentage of patients showing a reduction of at least 3 points of their skin discomfort in the feet and scalp, measured with the Analogue Visual Scale (0-10) of cutaneous discomfort

    Time frame: day 30

  17. 32-item Ichthyosis Quality of Life questionnaire (IQoL-32)

    Variation of patient's quality of life, measured by the ichthyosis specific quality of life questionnaire (IQoL-32)

    Time frame: 30 days after treatment

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05979506
Responsible party
Sponsor
First posted
Aug 7, 2023
Start date
Feb 2, 2024
Primary completion
Oct 10, 2026 (estimated)
Completion
Oct 10, 2026 (estimated)
Last update
Apr 13, 2026

Study contacts

Anne-Marie TRANIER
Contact
tranier.am@chu-toulouse.fr
05 67 77 14 57
RASMUS Lysa
Contact
rasmus.l@chu-toulouse.fr
Anne-Marie TRANIER
principal investigator · University Hospital, Toulouse
Lysa RASMUS
principal investigator · University Hospital, Toulouse

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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