NCT00177268

Brief Summary

This is a tissue, urine, and blood banking protocol for cutaneous t-cell lymphoma (CTCL), eczema, and atopic dermatitis patients for current and future research.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
69mo left

Started Oct 2004

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

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 Progress79%
Oct 2004Jan 2032

Study Start

First participant enrolled

October 1, 2004

Completed
12 months until next milestone

First Submitted

Initial submission to the registry

September 12, 2005

Completed
3 days until next milestone

First Posted

Study publicly available on registry

September 15, 2005

Completed
24.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2030

Expected
2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2032

Last Updated

December 30, 2025

Status Verified

December 1, 2025

Enrollment Period

25.3 years

First QC Date

September 12, 2005

Last Update Submit

December 23, 2025

Conditions

Keywords

Cutaneous T-cell LymphomaSezary SyndromeMycosis FungoidesBlood/tissue bankingeczemaatopic dermatitis

Outcome Measures

Primary Outcomes (1)

  • Proteomics of Cutaneous T-cell lymphoma

    Proteomic variables will be measured in blood and tissue of consented CTCL patients.

    Ongoing

Study Arms (1)

CTCL, atopic dermatitis, eczema

Those subjects with cutaneous t-cell lymphoma and Sezary syndrome, atopic dermatitis, or eczema may participate as appropriate with the potential for blood, tissue or urine sampling.

Other: Blood draw, skin biopsy or urine collection

Interventions

Up to 9 blood draws/year of 60 ml of whole blood. One 6 mm punch biopsy may be obtained up to 4 times per year.

CTCL, atopic dermatitis, eczema

Eligibility Criteria

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

Subjects with cutaneous t-cell lymphoma and/or Sezary syndrome and atopic dermatitis or eczema patients

You may qualify if:

  • or older
  • able and willing to provide informed consent
  • diagnosed with CTCL
  • diagnosed with either atopic dermatitis or eczema

You may not qualify if:

  • Lack of CTCL, atopic dermatitis, or eczema diagnosis in medical record

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Pittsburgh Medical Center

Pittsburgh, Pennsylvania, 15213, United States

RECRUITING

Biospecimen

Retention: SAMPLES WITHOUT DNA

White blood cells and/or skin biopsy tissue are retained.

MeSH Terms

Conditions

Lymphoma, T-Cell, CutaneousSezary SyndromeMycosis FungoidesEczemaDermatitis, Atopic

Interventions

Blood Specimen CollectionUrine Specimen Collection

Condition Hierarchy (Ancestors)

Lymphoma, T-CellLymphoma, Non-HodgkinLymphomaNeoplasms by Histologic TypeNeoplasmsLymphoproliferative DisordersLymphatic DiseasesHemic and Lymphatic DiseasesImmunoproliferative DisordersImmune System DiseasesDermatitisSkin DiseasesSkin and Connective Tissue DiseasesSkin Diseases, EczematousSkin Diseases, GeneticGenetic Diseases, InbornCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesHypersensitivity, ImmediateHypersensitivity

Intervention Hierarchy (Ancestors)

Specimen HandlingClinical Laboratory TechniquesDiagnostic Techniques and ProceduresDiagnosisPuncturesSurgical Procedures, OperativeInvestigative Techniques

Study Officials

  • Oleg E Akilov, M.D., PhD

    University of Pittsburgh

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Charity L Ruhl, LPN

CONTACT

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor of Dermatology

Study Record Dates

First Submitted

September 12, 2005

First Posted

September 15, 2005

Study Start

October 1, 2004

Primary Completion (Estimated)

January 1, 2030

Study Completion (Estimated)

January 1, 2032

Last Updated

December 30, 2025

Record last verified: 2025-12

Locations