Collection of Saliva and/ or Peripheral Blood From Healthy Volunteers for Research

NCT ID: NCT01851382

Last Updated: 2022-07-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

29 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-05-15

Study Completion Date

2015-02-12

Brief Summary

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Background:

\- Researchers often collect samples from healthy volunteers to further their research. These samples can help better understand serious side effects and complications of transplant treatments in patients. This study will collect saliva samples from healthy volunteers.

Objectives:

\- To collect saliva and blood samples from healthy volunteers for research studies.

Eligibility:

\- Healthy men ages 30-70 years for Phase I of the study.

Design:

* Participants will be screened with a medical history questionnaire. They will also have a brief oral exam to check for any mouth infection.
* Participants will provide a saliva sample. The collection process will take about 5 minutes.
* No treatment will be given as part of this study.

Detailed Description

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Background:

* Chronic graft-versus-host disease (cGVHD) is a severe immunological complication that occurs after allogeneic hematopoietic stem cell transplantation (HSCT). Although oral cGVHD occurs in \>25% of cGVHD patients and leads to decreased quality of life, its etiology is poorly understood.
* The primary objective of the present protocol is to enroll normal volunteers who will contribute a saliva and/or blood sample in order to compare its characteristics with those of patients with and without chronic GVHD after allogeneic HSCT. The normal control saliva and blood samples will provide a standard of comparison for patient saliva and blood samples from ongoing NCI cGVHD related protocols.

Objective:

-To collect approximately 5 ml of saliva and/or 18 cc peripheral blood from healthy volunteers as needed to support research activities.

Eligibility:

* Healthy individuals (including employees) all racial/ethnic groups, aged 18 years or older.
* Volunteers must be willing to undergo saliva and peripheral blood collection.
* No active illnesses, immunodeficiency, history of opportunistic infection, autoimmune disease, immunosuppressive medications or prior organ, bone marrow or peripheral blood stem cell transplant.
* Ability of subject to understand and provide written informed consent.
* Phase I of the study will be restricted to males, age 30-70 years

Design:

* Healthy volunteers will be offered the opportunity to participate in this protocol.
* A basic clinical dental assessment will be done.
* Saliva samples will be collected from the consenting subject.
* Peripheral blood samples may be collected from the consenting subject at the same visit.
* Protein assays will be performed on the collected saliva and blood samples.

Conditions

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Graft vs Host Disease Healthy Volunteer Graft-Versus-Host Disease

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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Cohort 1

Healthy volunteers.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Healthy individuals (including employees) and other healthy volunteers from all racial/ethnic groups
* Age 18 years and older, with possible restriction for age-matching to patient samples.
* Ability of subject to understand and provide written informed consent
* Subjects must participate fully and be willing to comply with the procedures of the protocol
* Phase I of the study will be restricted to males, age 30-70 years.

Exclusion Criteria

* Active systemic illnesses, immunodeficiency, history of opportunistic infection, autoimmune disease, immunosuppressive medications
* Prior organ, bone marrow or peripheral blood stem cell transplant
* Acute dental infection
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Institute (NCI)

NIH

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Steven Z Pavletic, M.D.

Role: PRINCIPAL_INVESTIGATOR

National Cancer Institute (NCI)

Locations

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National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, Maryland, United States

Site Status

Countries

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United States

References

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Mays JW, Fassil H, Edwards DA, Pavletic SZ, Bassim CW. Oral chronic graft-versus-host disease: current pathogenesis, therapy, and research. Oral Dis. 2013 May;19(4):327-46. doi: 10.1111/odi.12028. Epub 2012 Oct 28.

Reference Type BACKGROUND
PMID: 23107104 (View on PubMed)

Bassim CW, Ambatipudi KS, Mays JW, Edwards DA, Swatkoski S, Fassil H, Baird K, Gucek M, Melvin JE, Pavletic SZ. Quantitative salivary proteomic differences in oral chronic graft-versus-host disease. J Clin Immunol. 2012 Dec;32(6):1390-9. doi: 10.1007/s10875-012-9738-4. Epub 2012 Jul 18.

Reference Type BACKGROUND
PMID: 22806177 (View on PubMed)

Related Links

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Other Identifiers

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13-C-0128

Identifier Type: -

Identifier Source: secondary_id

130128

Identifier Type: -

Identifier Source: org_study_id

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