NCT06410053

Brief Summary

The All-Ireland Infectious Diseases (AIID) Cohort is a multicentre, prospective, longitudinal observational cohort that enrols consecutive adult subjects attending participating institutions for infectious disease services. This is an ongoing prospective observational cohort of unlimited duration.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
10,000

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Mar 2011

Longer than P75 for all trials

Geographic Reach
1 country

9 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2011

Completed
12.1 years until next milestone

First Submitted

Initial submission to the registry

April 5, 2023

Completed
1.1 years until next milestone

First Posted

Study publicly available on registry

May 10, 2024

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2024

Completed
Last Updated

May 10, 2024

Status Verified

May 1, 2024

Enrollment Period

13.8 years

First QC Date

April 5, 2023

Last Update Submit

May 8, 2024

Conditions

Keywords

Human Immunodeficiency virusCOVID-19Viral hepatitisSkin and soft tissue infectionsBone infection

Outcome Measures

Primary Outcomes (1)

  • Establishment of data rich cohort

    Overall number of recruited participants and number of recruited participants with major conditions (COVID-19, HIV, TB)

    through study completion, an average of 1 year

Secondary Outcomes (2)

  • Cohort retention

    through study completion, an average of 1 year

  • Cohort associated metadata

    through study completion, an average of 1 year

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

All adult patients attending Clinical Services relating to infectious diseases at participating hospitals in Ireland who provide written informed consent.

You may qualify if:

  • ≥ 18 years of age patients attending clinical services of participating institutions with issues related to infectious diseases.
  • Willing and able to provide informed consent or
  • Provide deferred assent if an incapacitated or unconscious patient is unable to provide informed consent

You may not qualify if:

  • Patients under 18 years of age
  • Patients with learning disabilities, mental illness, or dementia

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (9)

Cork University Hospital

Cork, Ireland

RECRUITING

Our Lady of Lourdes Hospital, Drogheda

Drogheda, Ireland

RECRUITING

St Vincent's University Hospital, Ireland

Dublin, D4, Ireland

RECRUITING

Mater Misericordiae University Hospital

Dublin, Dublin 7, Ireland

RECRUITING

Beaumont Hospital

Dublin, Ireland

RECRUITING

Children's Health Ireland at Crumlin

Dublin, Ireland

RECRUITING

St James's Hospital

Dublin, Ireland

RECRUITING

St Luke's General Hospital, Kilkenny

Kilkenny, Ireland

RECRUITING

Wexford General Hospital

Wexford, Ireland

RECRUITING

Related Links

Biospecimen

Retention: SAMPLES WITH DNA

1. Blood sample to be prepared as plasma, serum and viable peripheral blood mononuclear cells (PBMC) for cryopreservation. 2. Respiratory samples (where relevant e.g., subject with respiratory viral infection or pulmonary TB) 3. Stool sample for later microbiome analysis (optional) 4. Urine 5. Swabs, including mucosal (e.g., ano-genital, naso-pharyngeal) and superficial (skin). In addition, where subjects undergo lumbar puncture testing as part of routine care, any excess available sample may also be stored. These stored samples provide the opportunity for future research studies investigating host factors associated with the response to infection.

MeSH Terms

Conditions

Communicable DiseasesAcquired Immunodeficiency SyndromeCOVID-19Soft Tissue Infections

Condition Hierarchy (Ancestors)

InfectionsDisease AttributesPathologic ProcessesPathological Conditions, Signs and SymptomsHIV InfectionsBlood-Borne InfectionsSexually Transmitted Diseases, ViralSexually Transmitted DiseasesLentivirus InfectionsRetroviridae InfectionsRNA Virus InfectionsVirus DiseasesSlow Virus DiseasesGenital DiseasesUrogenital DiseasesImmunologic Deficiency SyndromesImmune System DiseasesPneumonia, ViralPneumoniaRespiratory Tract InfectionsCoronavirus InfectionsCoronaviridae InfectionsNidovirales InfectionsLung DiseasesRespiratory Tract Diseases

Study Officials

  • Patrick Mallon, PhD, FRCPI

    UCD

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Aoife Cotter, PhD

CONTACT

Alan Macken

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 5, 2023

First Posted

May 10, 2024

Study Start

March 1, 2011

Primary Completion

December 1, 2024

Study Completion

December 1, 2024

Last Updated

May 10, 2024

Record last verified: 2024-05

Locations