Bacteremia and Procalcitonin Levels in Peroral Endoscopic Myotomy for Achalasia
Primary Purpose
Esophageal Achalasia
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
no antibiotic prophylaxis
second-generation cephalosporin
Sponsored by
About this trial
This is an interventional prevention trial for Esophageal Achalasia focused on measuring Esophageal Achalasia, antibiotic prophylaxis, blood culture, procalcitonin levels
Eligibility Criteria
Inclusion Criteria:
- Clinical diagnosis of esophageal achalasia
- Ready to have the treatment as POEM and no contraindication of POEM
- Ability to get informed consent
Exclusion Criteria:
- Patients who had indications for antibiotic prophylaxis as determined by the American Society for Gastrointestinal Endoscopy
- Patients who had received antibiotics for any reason within the previous 7days
- Patients who had possible signs of any infection at the time of the procedure
- Patients who had chronic inflammatory diseases need hormonotherapy : such as rheumatic arthritis or inflammatory bowel diseases.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
no antibiotic prophylaxis
second-generation cephalosporin
Arm Description
These patients are in no antibiotic prophylaxis group will not be administered antibiotic prophylactically.
These patients are in antibiotic prophylaxis group will be administered second-generation cephalosporin prophylactically.
Outcomes
Primary Outcome Measures
Blood culture positive incidence
To compare the positive incidence of blood cultures between antibiotic prophylaxis and no antibiotic prophylaxis.
Secondary Outcome Measures
procalcitonin level
To observe the changes of procalcitonin levels after POEM in which no antibiotic is administered.
To compare the procalcitonin levels between antibiotic prophylaxis and no antibiotic prophylaxis.
Full Information
NCT ID
NCT01750385
First Posted
November 20, 2012
Last Updated
December 12, 2012
Sponsor
Shanghai Zhongshan Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01750385
Brief Title
Bacteremia and Procalcitonin Levels in Peroral Endoscopic Myotomy for Achalasia
Official Title
Bacteremia and Procalcitonin Levels in Peroral Endoscopic Myotomy for Achalasia
Study Type
Interventional
2. Study Status
Record Verification Date
December 2012
Overall Recruitment Status
Unknown status
Study Start Date
October 2012 (undefined)
Primary Completion Date
April 2013 (Anticipated)
Study Completion Date
August 2013 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Zhongshan Hospital
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Peroral Endoscopic Myotomy (POEM) is a novel, promising endoscopic technique for achalasia because it is safer and more effective than traditional Heller's myotomy. However, the issue of antibiotic prophylaxis in POEM has evoked considerable controversy recently. Therefore, we conduct this study to elucidate the status of POEM-related bacteremia and procalcitonin levels in order to preliminary observe whether antibiotic prophylaxis is needed.
Detailed Description
Objective: To elucidate the status of POEM-related bacteremia and procalcitonin levels in order to preliminary observe whether antibiotic prophylaxis is needed.
Interventions: Patients with achalasia diagnosed by symptoms, endoscopy and barium swallow eligible for POEM are randomized to either use antibiotic prophylactically or not.
Main outcome measurements: Blood culture positive incidence; secondary outcomes are procalcitonin levels, C-reactive protein levels, white blood cell counts and so on.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Achalasia
Keywords
Esophageal Achalasia, antibiotic prophylaxis, blood culture, procalcitonin levels
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
no antibiotic prophylaxis
Arm Type
Active Comparator
Arm Description
These patients are in no antibiotic prophylaxis group will not be administered antibiotic prophylactically.
Arm Title
second-generation cephalosporin
Arm Type
Active Comparator
Arm Description
These patients are in antibiotic prophylaxis group will be administered second-generation cephalosporin prophylactically.
Intervention Type
Drug
Intervention Name(s)
no antibiotic prophylaxis
Intervention Description
These patients are in no antibiotic prophylaxis group will not be administered antibiotic prophylactically.
Intervention Type
Drug
Intervention Name(s)
second-generation cephalosporin
Intervention Description
These patients are in antibiotic prophylaxis group will be administered second-generation cephalosporin prophylactically.
Primary Outcome Measure Information:
Title
Blood culture positive incidence
Description
To compare the positive incidence of blood cultures between antibiotic prophylaxis and no antibiotic prophylaxis.
Time Frame
after 12 hours of POEM
Secondary Outcome Measure Information:
Title
procalcitonin level
Description
To observe the changes of procalcitonin levels after POEM in which no antibiotic is administered.
To compare the procalcitonin levels between antibiotic prophylaxis and no antibiotic prophylaxis.
Time Frame
after 12 hours of POEM
Other Pre-specified Outcome Measures:
Title
clinical manifestation
Description
To observe the changes of temperature, heart rate, respiratory rate, white blood cell counts, neutrophile granulocyte counts in perioperative period.
Time Frame
during hospital stay and up to 1 week
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:
Clinical diagnosis of esophageal achalasia
Ready to have the treatment as POEM and no contraindication of POEM
Ability to get informed consent
Exclusion Criteria:
Patients who had indications for antibiotic prophylaxis as determined by the American Society for Gastrointestinal Endoscopy
Patients who had received antibiotics for any reason within the previous 7days
Patients who had possible signs of any infection at the time of the procedure
Patients who had chronic inflammatory diseases need hormonotherapy : such as rheumatic arthritis or inflammatory bowel diseases.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ping-Hong Zhou, M.D,PhD
Organizational Affiliation
Fudan University
Official's Role
Study Director
12. IPD Sharing Statement
Learn more about this trial
Bacteremia and Procalcitonin Levels in Peroral Endoscopic Myotomy for Achalasia
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