Global Registry of Alopecia Areata Disease Severity and treatment Safety - Ireland (GRASS - Ireland)
GRASS-Ireland is an observational study collecting and analysing the data of adults and children with Alopecia Areata (AA) in Ireland over their lifetime.
As an encounter-based registry, data will be collected from each interaction for AA-specific care by investigators at selected sites, on an ongoing basis using a secure, online platform.
This data will be used to better understand the background, treatments and outcomes of people with AA. This will be used for advocacy and to support planning of services, management and assistance of this group. The registry may also be useful to identify patients who could participate in suitable clinical trials and support pharmacovigilance studies.
The information generated will be of interest to physicians, researchers, health service providers, regulatory authorities, the pharmaceutical industry and persons with AA. It will guide the development of international best practice standards and the treatment strategies to meet these.
GRASS – Ireland is a founding member of a collaborative, global network of sovereign GRASS registries that aim to better understand the health, well-being and treatment of people with AA.
**Purpose:** Alopecia Areata (AA) is an autoimmune hair loss condition that affects approximately 2% of the population. It typically presents with patchy to complete loss of scalp hair, though other hair bearing sites and the nails can also be affected. Research shows that AA has a major impact on physical and psychological health. The aim of this project is to establish an Irish AA patient registry, which enables clinicians to record long-term, real-world data.This data will be pivotal in informing clinical
**Coverage:** National and International, the study duration is ongoing.
- Organization
- National Skin Registry Solutions
- License
- Creative Commons Attribution Share-Alike
Metadata
| Field | Value |
|---|---|
| Access Rights | http://publications.europa.eu/resource/authority/access-right/PUBLIC |
| Frequency | http://publications.europa.eu/resource/authority/frequency/MONTHLY |
| Id | 780c4bd2-d89f-497a-a7e6-b5f40433ad0f |
| Identifier | NDC-0032 |
| Isopen | True |
| Issued | 2021-01-01 |
| License Id | cc-by-sa |
| License Title | Creative Commons Attribution Share-Alike |
| License Url | http://www.opendefinition.org/licenses/cc-by-sa |
| Max Typical Age | 85 |
| Metadata Created | 2026-03-19T17:17:17.770981 |
| Metadata Modified | 2026-03-19T17:17:17.770984 |
| Min Typical Age | 0 |
| Modified | 2025-09-19 |
| Name | global-registry-of-alopecia-areata-disease-severity-and-treatment-safety-ireland-32 |
| Notes | GRASS-Ireland is an observational study collecting and analysing the data of adults and children with Alopecia Areata (AA) in Ireland over their lifetime. As an encounter-based registry, data will be collected from each interaction for AA-specific care by investigators at selected sites, on an ongoing basis using a secure, online platform. This data will be used to better understand the background, treatments and outcomes of people with AA. This will be used for advocacy and to support planning of services, management and assistance of this group. The registry may also be useful to identify patients who could participate in suitable clinical trials and support pharmacovigilance studies. The information generated will be of interest to physicians, researchers, health service providers, regulatory authorities, the pharmaceutical industry and persons with AA. It will guide the development of international best practice standards and the treatment strategies to meet these. GRASS – Ireland is a founding member of a collaborative, global network of sovereign GRASS registries that aim to better understand the health, well-being and treatment of people with AA. **Purpose:** Alopecia Areata (AA) is an autoimmune hair loss condition that affects approximately 2% of the population. It typically presents with patchy to complete loss of scalp hair, though other hair bearing sites and the nails can also be affected. Research shows that AA has a major impact on physical and psychological health. The aim of this project is to establish an Irish AA patient registry, which enables clinicians to record long-term, real-world data.This data will be pivotal in informing clinical **Coverage:** National and International, the study duration is ongoing. |
| Num Resources | 0 |
| Num Tags | 3 |
| Number Of Records | 450585 |
| Number Of Unique Individuals | 311055 |
| Private | False |
| Provenance | Enrolment in the registry is subject to a process of gaining informed explicit consent from patients or their parents or carer (if under 18). Participation is voluntary. The data is then collected from the patients charts after their standard clinic visits and entered onto the registry platform. Data is collected from patient medical charts and input into a secure internet-based computer database. Data collection is undertaken by GRASS-Ireland registry data collectors. Data is collected on a continual basis throughout the year and GRASS-Ireland data collectors collect data on an encounter basis. |
| Title | Global Registry of Alopecia Areata Disease Severity and treatment Safety - Ireland (GRASS - Ireland) |
| Type | dataset |
No history available for this dataset.