Patient Reported Outcomes in Living Donor Lung Transplantation
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Purpose
The purpose of the present study is to investigate how the health of donors in living donor lung transplantation will change after transplant operations.
| Condition | Intervention |
|---|---|
|
Lung Transplantation |
Procedure: Living donor lung transplantation |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Analysis of Patient Reported Outcomes in Living Donor Lung Transplantation |
- Change in health status [ Time Frame: At entry and every year for 5 years ] [ Designated as safety issue: No ]
- Change in dyspnea [ Time Frame: At entry and every year for 5 years ] [ Designated as safety issue: No ]
- Change in psychological status [ Time Frame: At entry and every year for 5 years ] [ Designated as safety issue: No ]
- Change in sleep quality [ Time Frame: At entry and every year for 5 years ] [ Designated as safety issue: No ]
- Prognosis [ Time Frame: At entry and every year for 5 years ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 40 |
| Study Start Date: | April 2009 |
| Estimated Study Completion Date: | March 2018 |
| Estimated Primary Completion Date: | December 2017 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
|
Living donor lung transplantation
Living lung transplantation donors
|
Procedure: Living donor lung transplantation
Living donor lung transplantation
Other Name: N.A.
|
Detailed Description:
In Japan, living donor lung transplantation has been established as an alternative therapy for brain-dead lung transplantation, as the number of organs for transplantation is absolutely short. However, how patient reported measurements including health status, dyspnea, psychological status and sleep would change after lung transplantation has not been well evaluated. Therefore, in the present study, we aim (1) to compare them before and after transplant operations and (2) to analyze how they will change for 5 years.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Kyoto University Hospital Clinic for Lung Transplantation
Inclusion Criteria:
- New donors for living donor lung transplantation
Exclusion Criteria:
- Inability to obtain informed consent
Contacts and Locations| Contact: Fengshi Chen, MD, PhD | +81 75 751 4975 | fengshic@kuhp.kyoto-u.ac.jp |
| Contact: Toru Oga, MD, PhD | +81 75 751 3852 | ogato@kuhp.kyoto-u.ac.jp |
| Japan | |
| Graduate School of Medicine, Kyoto University | Recruiting |
| Kyoto, Japan | |
| Contact: Fengshi Chen, MD, PhD +81 75 751 4975 fengshic@kuhp.kyoto-u.ac.jp | |
| Contact: Toru Oga, MD, PhD +81 75 751 3852 ogato@kuhp.kyoto-u.ac.jp | |
| Sub-Investigator: Toru Bando, MD, PhD | |
| Sub-Investigator: Izumi Matsumoto | |
| Sub-Investigator: Hiroaki Sakai, MD | |
| Study Chair: | Hiroshi Date, MD, PhD | Graduate School of Medicine, Kyoto University |
More Information
No publications provided
| Responsible Party: | Toru Oga, Department of Respiratory Care and Sleep Control Medicine, Kyoto University, Graduate School of Medicine |
| ClinicalTrials.gov Identifier: | NCT00905697 History of Changes |
| Other Study ID Numbers: | E561kyoto |
| Study First Received: | May 18, 2009 |
| Last Updated: | March 25, 2013 |
| Health Authority: | Japan: Institutional Review Board |
Keywords provided by Kyoto University, Graduate School of Medicine:
|
Living donor lung transplantation Health-related quality of life Prognosis Patient reported outcome |
ClinicalTrials.gov processed this record on June 18, 2013