Epinephrine Sprayed on the Papilla for the Prevention of Post-ERCP Pancreatitis
Primary Purpose
Post-ERCP Acute Pancreatitis
Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
epinephrine
normal saline
Sponsored by
About this trial
This is an interventional prevention trial for Post-ERCP Acute Pancreatitis
Eligibility Criteria
Inclusion Criteria:
- Males and females, age > 18 years.
- Normal amylase level before undergoing ERCP.
- Signed inform consent form and agreed to follow-up on time.
Exclusion Criteria:
- Pregnancy or history of allergy to epinephrine.
- Medical or psychological condition that would not permit the patient to complete the study or sign the informed consent.
- Patients involved in other study within 60 days.
- Billroth II or Roux-en-Y anatomy
- Acute pancreatitis.
- All contraindications to epinephrine.
Sites / Locations
- Department of General Surgery, Anhui Provincial Hospital Affiliated with Anhui Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Drug: epinephrine
Drug: normal saline
Arm Description
20-mL irrigation with epinephrine diluted to 0.02% in saline over the entire papilla
20-mL irrigation with physiological saline over the entire papilla
Outcomes
Primary Outcome Measures
The prophylaxis effect of epinephrine sprayed on the papilla on post-ERCP pancreatitis
If the serum amylase of patients elevation and 3 times higher than the normal values after ERCP 24 hours in high risk patients, who also have clinical symptoms, without other acute abdominal diseases,such as gastrointestinal perforation,acute cholecystitia and acute cholangitis and etc. In this condition, it will be defined PEP(post-ERCP pancreatitis). Descriptive statistics will be produced for all continuous variables. Frequency tables of number (N) and percentage of subjects will be produced for all categorical variables.
Descriptive statistics will be produced for all continuous variables. Frequency tables of number (N) and percentage of subjects will be produced for all categorical variables.
Secondary Outcome Measures
Compare epinephrine group with control group on the incidence of hyperamylasemia/adverse events.
Hyperamylasemia will be defined as the serum amylase 3 times more than the upper normal values, without clinical symptoms. During the study, any unexpected medical issue will be called adverse event.
Descriptive statistics will be produced for all continuous variables. Frequency tables of number (N) and percentage of subjects will be produced for all categorical variables.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02839356
Brief Title
Epinephrine Sprayed on the Papilla for the Prevention of Post-ERCP Pancreatitis
Study Type
Interventional
2. Study Status
Record Verification Date
July 2016
Overall Recruitment Status
Unknown status
Study Start Date
July 2016 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Anhui Provincial Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Post-endoscopic retrograde cholangiopancreatography (ERCP) pancreatitis (PEP) has been a well-recognized complication with significant morbidity and even mortality. A variety of possible mechanisms has been suggested in the occurrence of pancreatitis, but papillary edema caused by manipulations during cannulation or endoscopic treatment has received the most attention. The papillary edema may cause temporary outflow obstruction of pancreatic juice, and then increase ductal pressure, resulting in the occurrence of pancreatitis. Topical application of epinephrine on the papilla may reduce papillary edema. Moreover, it is reported that epinephrine sprayed on the papilla may be effective to prevent PEP. However, it is still unclear that epinephrine sprayed on the papilla can prevent acute pancreatitis after endoscopic retrograde cholangiopancreatography. We therefore designed a prospective randomized trial to determine whether epinephrine sprayed on the papilla prevent PEP after ERCP.
Detailed Description
Between July 2016 and December 2017, 670 consecutive patients older than 18 years who are scheduled to undergo diagnostic or therapeutic ERCP at the Anhui Provincial Hospital will be recruited for the study. Patients were randomized using opaque, sealed envelopes containing random numbers assigning them to undergo a spray of epinephrine (epinephrine group) or saline (control group) on the major papilla. A two proportion equality test will be conducted to explore whether incidence rates are different. Descriptive statistics including number (N), mean, median, standard deviation, minimum and maximum, will be produced for all continuous variables. Frequency tables of number (N) and percentage of subjects will be produced for all categorical variables.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post-ERCP Acute Pancreatitis
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
670 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Drug: epinephrine
Arm Type
Experimental
Arm Description
20-mL irrigation with epinephrine diluted to 0.02% in saline over the entire papilla
Arm Title
Drug: normal saline
Arm Type
Placebo Comparator
Arm Description
20-mL irrigation with physiological saline over the entire papilla
Intervention Type
Drug
Intervention Name(s)
epinephrine
Intervention Description
20-mL irrigation with epinephrine diluted to 0.02% in saline over the entire papilla
Intervention Type
Drug
Intervention Name(s)
normal saline
Intervention Description
20-mL irrigation with physiological saline over the entire papilla
Primary Outcome Measure Information:
Title
The prophylaxis effect of epinephrine sprayed on the papilla on post-ERCP pancreatitis
Description
If the serum amylase of patients elevation and 3 times higher than the normal values after ERCP 24 hours in high risk patients, who also have clinical symptoms, without other acute abdominal diseases,such as gastrointestinal perforation,acute cholecystitia and acute cholangitis and etc. In this condition, it will be defined PEP(post-ERCP pancreatitis). Descriptive statistics will be produced for all continuous variables. Frequency tables of number (N) and percentage of subjects will be produced for all categorical variables.
Descriptive statistics will be produced for all continuous variables. Frequency tables of number (N) and percentage of subjects will be produced for all categorical variables.
Time Frame
PEP occurence rate at 24 h after ERCP in two groups.
Secondary Outcome Measure Information:
Title
Compare epinephrine group with control group on the incidence of hyperamylasemia/adverse events.
Description
Hyperamylasemia will be defined as the serum amylase 3 times more than the upper normal values, without clinical symptoms. During the study, any unexpected medical issue will be called adverse event.
Descriptive statistics will be produced for all continuous variables. Frequency tables of number (N) and percentage of subjects will be produced for all categorical variables.
Time Frame
the incidence of hyperamylasemia/adverse events at 24 h after ERCP in two groups
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Males and females, age > 18 years.
Normal amylase level before undergoing ERCP.
Signed inform consent form and agreed to follow-up on time.
Exclusion Criteria:
Pregnancy or history of allergy to epinephrine.
Medical or psychological condition that would not permit the patient to complete the study or sign the informed consent.
Patients involved in other study within 60 days.
Billroth II or Roux-en-Y anatomy
Acute pancreatitis.
All contraindications to epinephrine.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Shao Feng, MD
Phone
8613033090788
Email
tagsmile1985@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shao Feng, MD
Organizational Affiliation
Department of General Surgery, Anhui Provincial Hospital Affiliated with Anhui Medical University
Official's Role
Study Director
Facility Information:
Facility Name
Department of General Surgery, Anhui Provincial Hospital Affiliated with Anhui Medical University
City
He Fei
State/Province
Anhui
ZIP/Postal Code
230001
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shao Feng, MD
Phone
8613033090788
Email
tagsmile1985@163.com
First Name & Middle Initial & Last Name & Degree
Shao Feng, MD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Epinephrine Sprayed on the Papilla for the Prevention of Post-ERCP Pancreatitis
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