RESULT (REflux Surgery in Lung Transplantation) Preliminary Study Protocol

Status:	Completed
Conditions:	Gastroesophageal Reflux Disease
Therapuetic Areas:	Gastroenterology
Healthy:	No
Age Range:	16 - Any
Updated:	5/27/2013
Start Date:	September 2011
End Date:	August 2013
Contact:	Robert D. Davis, MD
Email:	davis053@mc.duke.edu
Phone:	919-681-4760

Prospective and Retrospective Study to Develop a Multi-center Randomized Study, to Determine if Prevention of GERD Related Aspiration by Surgical Fundoplication Improves Lung Allograft Function

The purpose of the prospective study is to collect information surrounding lung transplant
in order to develop a randomized study to determine if prevention of gastroesophageal reflux
disease (GERD) related aspiration (stomach acid coming up from the stomach into the
esophagus) by surgical fundoplication improves lung rejection. Lung transplantation has
evolved into an effective treatment for patients with end-stage lung disease; however, a
significant limitation to long-term survival is patients develop a condition of scarring
known as chronic lung rejection, which can cause lung function to deteriorate, thereby
reducing a patient's chances for survival. Preliminary research has shown a correlation
between the presence of gastroesophageal reflux disease (GERD) and impaired early lung
rejection as assessed by a breathing test, FEV1 (the amount of forced expired air volume in
1 second).

The Investigator is interested in learning more about this condition and the potential for
aspiration (inhaling fluid) injury. The primary goal of this preliminary study will be to
identify aspiration markers that are correlated with adverse clinical outcomes (increased
early rejection, decreased FEV1) that may be used as inclusion criteria for the future
randomized trial.

The purpose of the retrospective study is to collect information surrounding lung transplant
in order to develop a randomized study to determine if prevention of gastroesophageal reflux
disease (GERD) related aspiration (stomach acid coming up from the stomach into the
esophagus) by surgical fundoplication improves lung rejection.

The goal of this retrospective data collection is to review the following:

1. subject outcome event rates for subjects with and without gastroesophageal reflux
disease (GERD) for survival, Bronchiolitis Obliterans Syndrome (BOS), acute rejection
and Forced Expiratory Volume in the first second (FEV-1),

2. the estimated treatment effect of fundoplication on the above event rates,

3. a threshold effect for Bronchiolitis Obliterans Syndrome (BOS) and/or death are more
likely to occur at higher or more proximal acid or non-acid contact times.

This data will be collected in order to better design and coordinate a multicenter
prospective study.

Prospective Group: Approximately 125 Bronchoalveolar Lavage (BAL) samples will be collected
from eligible subjects at the time of clinical bronchoscopies and will be within 2 weeks of
their esophageal study. The Bronchoalveolar Lavage (BAL) samples will be assayed for bile
acids; pepsin, pepsinogen I and II; trypsin; gastrin, and Lipopolysaccharide (LPS) content.
Short-term clinical outcome measures including acute rejection episodes, and Forced
Expiratory Volume in the first second (FEV-1) at one year will be collected. Correlation
between markers of reflux and aspiration will be analyzed.

Retrospective Group: Up to 800 charts within the past 5 years will be reviewed for 1)
subject outcome event rates for subjects with and without Gastroesophageal Reflux Disease
(GERD) for survival, Bronchiolitis Obliterans Syndrome (BOS), acute rejection and Forced
Expiratory Volume in the first second (FEV-1), 2) what is the estimated treatment effect of
fundoplication on the above event rates, 3) is there a threshold effect such that events
such as BOS and death are more likely to occur only at higher or more proximal acid or
non-acid contact times. This review will better address the role of Gastroesophageal Reflux
Disease (GERD) in lung allograft failure, the clinical utility of surgical fundoplication in
preventing lung allograft injury, and the role that acid and non-acid reflux as related to
aspiration causes lung allograft injury as it relates to a wider population.

Inclusion Criteria:

1. Male or non-pregnant female subject

2. 16 years of age

3. Recipient of a double-lung transplant

4. Previously have a 24-hour esophageal pH and/or impedance probe study within 12 months
prior to transplant and/or within 12 months following transplantation. If the subject
expired prior to 12 months from transplant date, they must have had a 24-hour
esophageal pH and/or impedance probe study to be eligible in the study.

Exclusion Criteria:

1. Recipient of a single-lung transplant

2. Recipient of a re-do lung transplant

3. Recipient of a double-lung/heart or double-lung/ other organ transplant

4. Do not have a 24-hour esophageal pH and/or impedance probe study within 12 months
pre-transplant or within 12 months following transplantation. The subject expired
less than 12 months post transplant without having a 24-hour esophageal pH and/or
impedance probe study

5. No Spirometry data is available for the subject

6. Subject who is participating in any other interventional clinical study

7. Unable to provide written informed consent or participate in long-term follow-up

We found this trial at

sites

Johns Hopkins University School of Medicine

733 North Broadway
Baltimore, Maryland 21205

(410) 955-3182