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Liver Transplant RecipientsNCT01525797

Blood Draw Study for Liver Transplant Patients

An observational study of Liver Transplant Recipients, run by Baylor Research Institute at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to see what a lab test will show and if there is a way to predict which patients will be more likely to have rejection after receiving a liver transplant. Read more about this study

Who is it for?
Ages 17 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Liver Transplant Recipients
How many people
221 participants
Where
1 siteUnited States
Study dates
15 Oct 2002to 4 Oct 2013
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 17 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: Liver Clinic

Who may be able to join

  • Received a liver Transplant

Who cannot join

  • Received Multiple Organ Transplant

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Baylor University Medical Center

    Dallas, Texas, 752245

Other trials in United States

About this study

Official title: Immunomonitoring of Transplant Patients

The purpose of this study is to see what a lab test will show and if there is a way to predict which patients will be more likely to have rejection after receiving a liver transplant.

Read the detailed description

The purpose of this study is simply to see what the new oligonucleotide microarrays will show when comparing the the different patient groups. The results of this study will be one of the first steps In exploring the potential use of this new test.

Keywords
Liver Transplant

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT01525797
Study groupRoleWhat they receive
ControlNot described
RejectionNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Identify signatures predictive of graft rejection or tolerance.

    Analyze the pattern of gene expression in patients undergoing solid organ transplantation

    Measured: 2 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted3 Feb 2012 (estimated)
  2. Study start15 Oct 2002
  3. Primary completion4 Oct 2013
  4. Study completion4 Oct 2013

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case only
Time perspective
Prospective
Enrolment
221 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01525797
Sponsor's protocol ID
002-197
Status last verified
Jan 2026
First submitted
11 May 2011
Last updated
26 Jan 2026
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

An observational study of Liver Transplant Recipients, run by Baylor Research Institute at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 26 Jan 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Identify signatures predictive of graft rejection or tolerance. (time frame: 2 years). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 Jan 2026.

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