search
Back to results

Transdermal Patch to Monitor Inflammatory Biomarkers of GVHD

Primary Purpose

Graft Versus Host Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
D-SQUAME Skin Sampling Discs
Sponsored by
Children's Hospital Medical Center, Cincinnati
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Graft Versus Host Disease focused on measuring children, bone marrow transplant, GVHD

Eligibility Criteria

3 Months - 30 Years (Child, Adult)All SexesAccepts Healthy Volunteers

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:

โ€ข 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:

โ€ข 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:

โ€ข Pre-existing dermatologic conditions. (E.g. eczema, psoriasis, acne etc.)

Sites / Locations

  • Cincinnati Children's Hospital Medical Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Acute Graft versus Host Disease

Chronic Graft versus Host Disease

Healthy Controls

Arm Description

This study arm includes patients who undergo allogeneic hematopoietic cell transplantation at CCHMC and develop acute graft versus host disease. Skin cell samples will be collected using the D-SQUAME Skin Sampling Discs. The first baseline skin sample will be obtained prior to the preparative regimen for stem cell transplant. Samples will be collected weekly after stem cell infusion until 8 weeks, if acute GVHD does not develop. If acute GVHD does develop, weekly samples will continue to be collected until resolution of acute GVHD or development of chronic GVHD, whichever occurs first. Blood samples will be collected at these same time points.

This study arm includes patients who undergo allogeneic hematopoietic cell transplantation at CCHMC and develop chronic graft versus host disease. Skin cell samples will be collected weekly for 4 weeks using the D-SQUAME Skin Sampling Discs. Blood samples will be collected at these same time points.

This study arm includes healthy age matched controls as comparisons to study participants who develop graft versus host disease. These controls may be either healthy age matched siblings of patients who develop acute graft versus host disease or healthy age matched siblings of patients that are seen in the bone marrow transplant, oncology, or hematology clinics. A one-time single skin cell sample will be collected using a D-SQUAME Skin Sampling Disc. Blood samples will not be collected from the healthy controls.

Outcomes

Primary Outcome Measures

CXCL10 in Skin
D-sqaume epidermal discs were used to assess CXCL10 levels from skin.
CXCL10 in Plasma
Plasma was used to assess CXCL10 levels from blood.

Secondary Outcome Measures

Full Information

First Posted
June 10, 2015
Last Updated
March 23, 2017
Sponsor
Children's Hospital Medical Center, Cincinnati
search

1. Study Identification

Unique Protocol Identification Number
NCT02511782
Brief Title
Transdermal Patch to Monitor Inflammatory Biomarkers of GVHD
Official Title
Use of a Transdermal Patch to Noninvasively Monitor Inflammatory Biomarkers of Acute and Chronic Skin GVHD
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Completed
Study Start Date
February 2012 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
October 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital Medical Center, Cincinnati

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Graft Versus Host Disease
Keywords
children, bone marrow transplant, GVHD

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
63 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Acute Graft versus Host Disease
Arm Type
Experimental
Arm Description
This study arm includes patients who undergo allogeneic hematopoietic cell transplantation at CCHMC and develop acute graft versus host disease. Skin cell samples will be collected using the D-SQUAME Skin Sampling Discs. The first baseline skin sample will be obtained prior to the preparative regimen for stem cell transplant. Samples will be collected weekly after stem cell infusion until 8 weeks, if acute GVHD does not develop. If acute GVHD does develop, weekly samples will continue to be collected until resolution of acute GVHD or development of chronic GVHD, whichever occurs first. Blood samples will be collected at these same time points.
Arm Title
Chronic Graft versus Host Disease
Arm Type
Experimental
Arm Description
This study arm includes patients who undergo allogeneic hematopoietic cell transplantation at CCHMC and develop chronic graft versus host disease. Skin cell samples will be collected weekly for 4 weeks using the D-SQUAME Skin Sampling Discs. Blood samples will be collected at these same time points.
Arm Title
Healthy Controls
Arm Type
Active Comparator
Arm Description
This study arm includes healthy age matched controls as comparisons to study participants who develop graft versus host disease. These controls may be either healthy age matched siblings of patients who develop acute graft versus host disease or healthy age matched siblings of patients that are seen in the bone marrow transplant, oncology, or hematology clinics. A one-time single skin cell sample will be collected using a D-SQUAME Skin Sampling Disc. Blood samples will not be collected from the healthy controls.
Intervention Type
Device
Intervention Name(s)
D-SQUAME Skin Sampling Discs
Intervention Description
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 Outcome Measure Information:
Title
CXCL10 in Skin
Description
D-sqaume epidermal discs were used to assess CXCL10 levels from skin.
Time Frame
At time of GVHD diagnosis.
Title
CXCL10 in Plasma
Description
Plasma was used to assess CXCL10 levels from blood.
Time Frame
At time of GVHD diagnosis.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Months
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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: โ€ข 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: โ€ข 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: โ€ข Pre-existing dermatologic conditions. (E.g. eczema, psoriasis, acne etc.)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pooja Khandelwal, MD
Organizational Affiliation
Children's Hospital Medical Center, Cincinnati
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cincinnati Children's Hospital Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45229
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Transdermal Patch to Monitor Inflammatory Biomarkers of GVHD

We'll reach out to this number within 24 hrs