Acute Pancreatitis Patient Registry To Examine Novel Therapies In Clinical Experiences 2

This study is an ancillary of APPRENTICE. This will be the international based study. The
initial study design with discussions about the different variables to be included into our
prospective database started during 2014 PancreasFest held in Pittsburgh, PA in late July
2014 under the sponsorship of Collaborative Alliance for Pancreatic Education and Research
(CAPER). Following this, a datasheet with variables was created, distributed through the
initial participants, and further suggestions and edits were made. We now plan to move ahead
with a web based seminar. All previous participants, as well as new investigators/centers
that have shown interest in participating throughout the world will be invited.University of
Pittsburgh will be responsible for collecting all required regulatory documents from other
sites. Developing templates for questionnaires and other data collection forms. Will train
approved sites on procedures. The coordinating center will be the recipient of de-identified
data and will not be involved in the collection of data.

Note that copies of training records, licenses, certificates should be maintained in the
study regulatory binder and are subject to audit by the Research Conduct and Compliance
Office (RCCO).

Inclusion Criteria:

1. The diagnosis of AP based upon presence of two out of the three following criteria:

1. Abdominal pain typical to AP

2. Serum amylase or lipase levels more than three times the upper limit of normal

3. Imaging findings suggestive of AP

2. Willingness to participate in the study and ability to sign informed consent by
patient or his/her proxy (if unable to speak).

Exclusion Criteria:

1. Age under 18 years

2. Unwilling to provide consent by patient or his/her proxy

3. Presence of pancreatic cancer

4. Presence of chronic pancreatitis

5. Occurrence of AP following a multiple trauma episode

6. Having history of organ transplant

7. Presence of any cancer which required chemotherapy or radiation therapy in the past
year.