Viral Triggers in Pediatric Lung Transplantation
![]() |
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT00891865 |
Recruitment Status :
Completed
First Posted : May 1, 2009
Last Update Posted : July 2, 2020
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease |
---|
Lung Transplant Bronchiolitis Obliterans Obliterative Bronchiolitis |
Study Type : | Observational |
Actual Enrollment : | 61 participants |
Observational Model: | Case-Only |
Time Perspective: | Prospective |
Official Title: | Viral Triggers of Alloimmunity and Autoimmunity in Pediatric Lung Transplantation (CTOTC-03) |
Study Start Date : | June 2009 |
Actual Primary Completion Date : | April 2015 |
Actual Study Completion Date : | April 2015 |

Group/Cohort |
---|
Pediatric lung transplantation |
- The earliest time to BOS or OB, retransplantation or death [ Time Frame: Within 24 months of transplant ]
- Time to each of the following events: BOS or OB, retransplantation or death [ Time Frame: Within 24 months of transplant ]
Biospecimen Retention: Samples With DNA

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | up to 21 Years (Child, Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Parent or legal guardian willing and able to provide informed consent
- Participant of first single or bilateral heart-lung transplant
Exclusion Criteria:
- Recipient of multi-organ transplant (aside from heart-lung)
- Condition or characteristic which in the opinion of the investigator makes the participant unlikely to complete the study

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00891865
United States, California | |
Stanford University | |
Palo Alto, California, United States, 94305 | |
United States, Massachusetts | |
Children's Hospital Boston | |
Boston, Massachusetts, United States | |
United States, Missouri | |
Washington University | |
Saint Louis, Missouri, United States, 63110 | |
United States, Ohio | |
Nationwide Children's Hospital | |
Columbus, Ohio, United States, 43205 | |
United States, Pennsylvania | |
Children's Hospital of Pennsylvania | |
Philadelphia, Pennsylvania, United States, 19104 | |
United States, Texas | |
Texas Children's Hospital | |
Houston, Texas, United States, 77030 |
Principal Investigator: | Stuart Sweet, MD, PhD | Washington University School of Medicine | |
Study Chair: | Lara Danziger-Isakov, MD, MPH | Children's Hospital Medical Center, Cincinnati |
Other Publications:
Responsible Party: | National Institute of Allergy and Infectious Diseases (NIAID) |
ClinicalTrials.gov Identifier: | NCT00891865 |
Other Study ID Numbers: |
DAIT CTOTC-03 |
First Posted: | May 1, 2009 Key Record Dates |
Last Update Posted: | July 2, 2020 |
Last Verified: | June 2020 |
lung transplant BOS OB Respiratory Viral Infection (RVI) Lung disease |
Bronchiolitis Bronchiolitis Obliterans Bronchitis Respiratory Tract Infections Infections |
Bronchial Diseases Respiratory Tract Diseases Lung Diseases, Obstructive Lung Diseases |