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Exploring Patient Reported Outcomes in Inherited Ichthyosis

Exploring Patient Reported Outcomes in Inherited Ichthyosis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06123091
Enrollment
20
Registered
2023-11-08
Start date
2023-09-01
Completion date
2024-12-01
Last updated
2023-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Congenital Ichthyosis

Brief summary

The goal of this observational study is to learn about the presence of extracutaneous manifestations in patients with congenital ichthyosis. The main question it aims to answer is: \- Do patients with congenital ichthyosis experience extracutaneous manifestations? Participants will fill in questionnaires in which the investigators will explore whether patients experience extracutaneous manifestations, and if so what these manifestations entail. Examples of such questions are whether patients experience (joint) pain or whether they experience hindrance due to their complaints.

Detailed description

There is only limited knowledge about extracutaneous manifestations in patients with congenital ichthyosis. With this study, the investigators aim to identify extracutaneous manifestations with questionaires based on patient reported outcomes. Secondary research questions include: * What is the prevalence of joint complaints in patients with congenital ichthyosis * What is the influence of ichthyosis on the quality of life patients experience Furthermore, the investigators aim to discover knowledge gaps in current patient management and possible areas of improvement in patient care towards healthcare professionals.

Interventions

OTHERQuestionnaires with patient reported outcome measures

Questionnaires to gain insight of the prevalence of extracutaneous manifestations and the impact of the disease on the quality of life.

Sponsors

Maastricht University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* 16 years and older * Clinically and genetically confirmed congenital ichthyosis

Exclusion criteria

* \<16 years of age * Not able to read Dutch * Not able to fill in questionnaires online or in print

Design outcomes

Primary

MeasureTime frameDescription
Extracutaneous manifestations in generalDay 1Evaluation of possible extracutaneous manifestations patients with congenital ichthyosis exhibit. This is measured by a questionnaire the investigators have composed. The questions entail patient reported outcomes on their general health and the health issues patients experience due to ichthyosis.

Secondary

MeasureTime frameDescription
Prevalence of joint complaints measured by the Early Arthritis Recognition Clinic questionnaireDay 1Prevalence of joint complaints measured by the Early Arthritis Recognition Clinic (EARC) questionnaire. The higher the total score, the more joint complaints patients with congenital ichthyosis experience.
Prevalence of joint complaints Early Arthritis for Psoriatic patients questionnaireDay 1Prevalence of joint complaints measured by the Early Arthritis for Psoriatic patients (EARP) questionnaire. The higher the total score, the more joint complaints patients with congenital ichthyosis experience.
Prevalence of joint complaints measured by the Clinical Arthritis Rule questionnaireDay 1Prevalence of joint complaints measured by the Clinical Arthritis Rule (CARE) questionnaire. The higher the total score, the more joint complaints patients with congenital ichthyosis experience.
Prevalence of joint complaints measured by the Psoriasis Epidemiology Screening ToolDay 1Prevalence of joint complaints measured by the Psoriasis Epidemiology Screening Tool (PEST). The higher the total score, the more joint complaints patients with congenital ichthyosis experience.
Impact of ichthyosis on quality of life measured by Skindex-29Day 1Evaluation of the quality of life of patients with congenital ichthyosis measured by the Skindex-29 questionnaire. Scores ranging from \>25 and \>44, where a higher score indicates that the skin disease has a bigger influence on their quality of life.
Prevalence of itch complaintsDay 1Evaluation of possible extracutaneous manifestations patients with congenital ichthyosis exhibit. This is measured by a numeric rating scale (NRS) of itch. The higher the outcome, the more itch patients experience
Prevalence of pain complaintsDay 1Evaluation of possible extracutaneous manifestations patients with congenital ichthyosis exhibit. This is measured by a numeric rating scale (NRS) of pain. The higher the outcome, the more pain the patients experience
Impact of ichthyosis on quality of lifeDay 1Evaluation of quality of life measured by the Dermatology Life Quality Index (DLQI) questionnaire. Scores range from 0-30, where a higher score indicates that the skin disease has a bigger influence on their quality of life.

Countries

Netherlands

Contacts

Primary ContactVanya Rossel, MD
vanya.rossel@mumc.nl+31(0)43-3877295

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026