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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02061215
Other study ID # 0742-13-EP
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date April 2014
Est. completion date July 14, 2015

Study information

Verified date August 2023
Source University of Nebraska
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Using novel CYTOF technology to measure a wide array of innate and adaptive cell proportions and cytokine levels, we plan a pilot study in old (>/=60 years) and young (20-40 years) renal transplant recipients who are cytomegalovirus (CMV) seropositive (regardless of donor serology). Viral load measurements will be performed at baseline prior to transplant (within 1 week),and then at 3, 7 and 10 months after transplant. It is expected that the patient will receive anti-CMV prophylaxis until 6 months post-transplant, so the latter two time points will reflect responses after "release" from antiviral suppression. Each patient will serve as their own control, with comparisons made between measurements at baseline and then at each timepoint. In addition, clinical data will be collected at the time points indicated, particularly renal function and the presence/absence of acute rejection.


Description:

Using novel CYTOF technology to measure a wide array of innate and adaptive cell proportions and cytokine levels, we plan a pilot study in old (>/=60 years) and young (20-40 years) renal transplant recipients who are CMV seropositive (regardless of donor serology). Viral load measurements will be performed at baseline prior to transplant (within 1 week),and then at 3, 7 and 10 months after transplant. It is expected that the patient will receive anti-CMV prophylaxis until 6 months post-transplant, so the latter two time points will reflect responses after "release" from antiviral suppression. Each patient will serve as their own control, with comparisons made between measurements at baseline and then at each timepoint. Blood from 10 patients in each age group will be studied, to collect virologic and immune response data: - CYTOF (broad array of measurements) - Tetramer assays (requires recipient HLA type of A1, A2, B7) - CMV viral load PCR - Response to pneumococcal antigens and inactivated influenza virus In addition, clinical data will be collected at the time points indicated,particularly renal function and the presence/absence of acute rejection.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date July 14, 2015
Est. primary completion date July 14, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria: 1. Adults young age 20-40 years and old >/= 60 years 2. Anticipate renal transplant within 2 weeks 3. CMV sero-positive renal transplant recipients 4. HLA type of A1, A2, B7 of recipient Exclusion Criteria: 1. Pediatric recipients 2. Multi-organ transplant recipients 3. Highly sensitized (antigen level) recipients 4. Prior organ transplant recipients 5. Patients who do not wish to participate in study, or who cannot consent to research 6. Patients with active CMV infection 7. Seronegative 8. HLA Type of organ recipient not corresponding to A1,A2, B7

Study Design


Related Conditions & MeSH terms

  • CMV Viral Loads in Seropositive Renal Transplant Recipients

Intervention

Other:
CMV viral load


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Nebraska

Outcome

Type Measure Description Time frame Safety issue
Primary CMV viral loads in younger seropositive kidney transplant recipients before transplant, during treatment and after therapy CMV viral loads in younger (age 20-40) seropositive kidney transplant recipients before renal transplant, during treatment with anti-viral therapy, and after release from therapy 1 year
Primary CMV viral loads in older seropositive kidney transplant recipients before transplant, during treatment and after therapy CMV viral loads in older (age >/= 60) seropositive kidney transplant recipients before renal transplant, during treatment with anti-viral therapy, and after release from therapy 1 year