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Completed

NCT Number: NCT02511782

Transdermal Patch to Monitor Inflammatory Biomarkers of GVHD

The aim of this study is to measure local inflammatory responses in patients undergoing an allogeneic stem cell transplant and attempt to define any set of biomarkers that are significantly altered in acute or chronic skin graft versus host disease.

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Key information

Age range

3 month–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cincinnati Children's Hospital Medical Center

Cincinnati, Ohio, 45229, United States

About this study

Acute skin graft versus host disease is a significant complication following allogeneic stem cell transplant. To date, there are no specific dermal biomarkers that predict or define the onset of acute skin graft versus host disease. The primary objective of this study is to observe the changes in the inflammatory environment of the skin during the process of acute and chronic skin graft versus host disease. This will be accomplished by using a non-invasive transdermal patch called D-Squame to analyze inflammatory cytokines and key epidermal proteins. Patients will be enrolled prior to receiving a stem cell transplant and followed weekly after stem cell infusion until day 99. If acute skin graft versus host disease develops, they will be followed weekly until resolution of acute graft versus host disease or development of chronic graft versus host disease, whichever occurs first. Patients with a diagnosis of chronic skin graft versus host disease will be enrolled and followed weekly until 4 weeks, irrespective of clinical course. In addition, healthy controls will be enrolled and used as comparators. The relevance of this study is to provide a better understanding of the local inflammatory environment induced by acute or chronic skin graft versus host disease. This is likely to enable the investigators to define a biomarker panel that predicts the onset of acute graft versus host disease rapidly and non-invasively.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for patients who may develop acute graft versus host disease:

  • All patients undergoing an allogeneic hematopoietic stem cell transplant at CCHMC.
  • All conditioning regimens are eligible.

Exclusion criteria

for patients who may develop acute graft versus host disease:

  • Pre-existing skin conditions like, but not limited to epidermolysis bullosa, psoriasis, acne, or cellulitis.

Inclusion criteria

for patients who have chronic graft versus host disease:

  • Bone marrow transplant performed at CCHMC or an outside institution.
  • Diagnosis of chronic skin graft versus host disease.

Exclusion criteria

for patients who have chronic graft versus host disease:

  • Bone marrow transplant performed for epidermolysis bullosa.

Inclusion criteria

for controls:

  • Healthy volunteers.
  • Age matched to the patients with existing acute skin graft versus host disease.

Exclusion criteria

for controls:

  • Pre-existing dermatologic conditions. (E.g. eczema, psoriasis, acne etc.)

Treatment and study plan

D-SQUAME Skin Sampling Discs

Device

A D-SQUAME Skin Sampling Disc is a noninvasive patch that collects skin cell samples when affixed to the superficial stratum corneum (top layer of skin). The patch is applied with gentle pressure to the desired quadrant of the forearm and removed 2 minutes after application.

Primary outcomes

  1. CXCL10 in Skin

    Time frame: At time of GVHD diagnosis.

    D-sqaume epidermal discs were used to assess CXCL10 levels from skin.

  2. CXCL10 in Plasma

    Time frame: At time of GVHD diagnosis.

    Plasma was used to assess CXCL10 levels from blood.

Sponsors and collaborators

Lead sponsor

Children's Hospital Medical Center, Cincinnati

Other

Registry information

Official study title

Use of a Transdermal Patch to Noninvasively Monitor Inflammatory Biomarkers of Acute and Chronic Skin GVHD

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Jul 30, 2015
Registry last updated
May 4, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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