Lung Transplant Specimen Repository and Data Registry Protocol
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Purpose
All patients enrolled in the registry will be recipients of single and double lung transplantation (bilateral sequential, heart-lung, or living related donor grafts). During the routine management of lung recipients frequent surveillance of the lung allograft is necessary. This routinely involves: measurement of pulmonary functions, chest radiography, collection of peripheral blood to assess other organ function and monitor therapeutic drug levels, and bronchoscopic evaluation allowing for collection of lung lavage fluid and lung tissue biopsy. This surveillance normally follows a set schedule during the first one to two years following the transplant procedure. Surveillance is routinely performed at weeks 2, 8, 12, 24, 36, and 52 during the first year following the transplant procedure. Additional surveillance may be performed at any time when clinically indicated for the optimal management of the recipient. Information and specimens collected from each of these encounters will be entered in the data registry and specimen repository.
| Condition |
|---|
|
Lung Transplantation |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Lung Transplant Specimen Repository and Data Registry Protocol |
- data registry and lung tissue repository [ Time Frame: ongoing ] [ Designated as safety issue: No ]
Biospecimen Retention: Samples With DNA
BAL specimen blood lung biopsy specimens
| Estimated Enrollment: | 100 |
| Study Start Date: | November 2005 |
| Estimated Study Completion Date: | December 2013 |
| Estimated Primary Completion Date: | December 2013 (Final data collection date for primary outcome measure) |
The collection of disposable lung allograft (transplant tissue samples), blood samples and information from medical records for storage, future analysis and research. Stored samples will be available to other researchers who have obtained separate review and approval from an ethics committee called an Institutional Review Board.
Immediately prior to the transplant surgery, the surgeon or pulmonologist will routinely examine the lungs via bronchoscopy during which subjects will be medicated for pain.
The samples that are obtained during this and post-surgery (clinically scheduled) bronchoscopies, including bronchial lavage, are either sent to pathology or are discarded if they do not qualify to go to pathology. For this research, the researchers are asking that the samples that do not qualify for pathology be placed into the repository instead of being thrown away.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
lung transplant recipients
Inclusion Criteria:
- recipients of single and double lung transplantation (bilateral sequential, heart-lung, or living related donor grafts).
Contacts and Locations| Contact: Karen Wood, MD | 614-293-4978 | karen.wood@osumc.edu |
| Contact: Janice Drake, CRTT | 614-293-4978 | janice.drake@osumc.edu |
| United States, Ohio | |
| The Ohio State University | Recruiting |
| Columbus, Ohio, United States, 43210 | |
| Contact: Janice Drake, CRTT 614-293-4978 janice.drake@osumc.edu | |
| Contact: Sharon Cheung, BS 614-366-2258 sharon.cheung@osumc.edu | |
| Principal Investigator: Karen L Wood, MD | |
| Principal Investigator: | David Nunley, MD | Ohio State University |
More Information
No publications provided
| Responsible Party: | Karen Wood, Karen Wood M.D., The Ohio State University |
| ClinicalTrials.gov Identifier: | NCT00816257 History of Changes |
| Other Study ID Numbers: | 2005H0101 |
| Study First Received: | December 31, 2008 |
| Last Updated: | May 2, 2013 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Ohio State University:
|
lung tissue repository |
ClinicalTrials.gov processed this record on May 22, 2013