Eczema Trial, Recruiting NCT00605878 Sponsor: National Human Genome Research Institute (NHGRI) Condition: Eczema
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Eczema Trial, Recruiting

NCT00605878
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • All participants must have a regular doctor or primary care professional who will continue their usual care and can receive updates and recommendations from the research team.
  • Group 1 (Healthy Adults): People who are male or female, aged 18 to 50 years at the time of joining.
  • Group 2 (Adults with Atopic Dermatitis/Eczema): People with a confirmed diagnosis of atopic dermatitis (eczema), a moderate to severe level of the condition (measured by a scoring system called SCORAD, with a score of 25 or above), and at least one affected area in the crook of the arm or behind the knee at the time of joining.
  • Group 3 (Healthy Children): Males or females aged 2 to 18 years.
  • Groups 4, 5, and 6 (Patients with specific immune conditions including AD, HIES, WAS, or DOCK8 deficiency): People with a diagnosis of one of these conditions confirmed through genetic testing, with or without eczema-like skin symptoms.

Who may not be able to join:

  • People who are currently receiving, or are planning to receive, certain experimental treatments, ultraviolet light therapy, monoclonal antibody therapy, or medicines that suppress the immune system within 7 days or 5 half-lives of starting the trial (whichever is the longer period).
  • People who have or have had cancer and have received chemotherapy or radiation treatment within the past 6 months.
  • People who have a history of bone marrow transplant or gene therapy.
  • Group 2 (Eczema patients specifically): People who are unable to stop taking oral antibiotics or oral steroids for at least 7 days before skin sampling, or who are unable to stop using topical steroids or certain skin creams (calcineurin inhibitors) on the specific small areas of skin to be sampled for at least 7 days beforehand.
  • Group 2 (Eczema patients specifically): People who have an underlying immune system deficiency, whether present from birth or caused by a medical treatment.
  • Groups 4, 5, and 6 (HIES, WAS, DOCK8 patients specifically): People who are unable to stop using topical steroids and moisturisers for preferably 7 days, but at a minimum 24 hours, before skin sampling.
  • Groups 1 and 3 (Healthy volunteers and healthy children specifically): People with unstable, uncontrolled, or ongoing medical conditions that require treatment or hospitalisation (the research doctor will assess this on a case-by-case basis).
  • Groups 1 and 3 specifically: People with an underlying immune system deficiency, whether present from birth or caused by a medical treatment.
  • Groups 1 and 3 specifically: People with a known ongoing skin condition such as eczema or psoriasis that could affect the study results (common short-term conditions like acne are generally permitted).
  • Groups 1 and 3 specifically: People who work directly in healthcare, live in healthcare or assisted living facilities, homeless shelters, jails, or prisons, or who have frequent contact with laboratory animals.
  • Groups 1 and 3 specifically: People who have asthma.
  • People who are female and have symptoms or hormone levels indicating they are going through perimenopause (the transition period before menopause).

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Julie A Segre, Ph.D., National Human Genome Research Institute (NHGRI)

Phone: (301) 827-2460

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
National Human Genome Research Institute (NHGRI)
Registry
ClinicalTrials.gov
Start date
22 January 2008

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Primary Immunodeficiency; Healthy volunteers

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov