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Enteral Nutrition in the Treatment of Pancreatic Fistulas - A Prospective Study (FIS-1)

Primary Purpose

Pancreatic Fistula

Status
Completed
Phase
Phase 4
Locations
Poland
Study Type
Interventional
Intervention
enteral nutrition
Parenteral nutrition
Sponsored by
Jagiellonian University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pancreatic Fistula focused on measuring pancreatic fistula

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • the presence of pancreatic fistula (PF) (verification of serum lipase concentration in drained fluid, findings on imaging modalities: endoscopic retrograde cholangiopancreatography (ERCP), helical computed tomography(hCT), magnetic reissonance imaging (MRI), ultrasonography (USG) or intraoperative surgeon's verification - any or some or all of them)
  • good general status (Karnoffsky > 80, Eastern Cooperative Oncology Group (ECOG) scale 0 or 1; see Appendix 2);
  • NRS and MUST evaluation - low/ medium risk patients not requiring parenteral nutrition as the essence treatment option,
  • no PF's complication requiring special treatment present, such as intraabdominal abscess formation, pleuropneumonia, bleeding, paralytic ileus, etc. Complications will be diagnosed and treated according to generally accepted medical knowledge, standards and procedures.
  • age below 80 and over 18;
  • in case of neoplastic patients: no confirmed neoplastic dissemination nor distant metastases;
  • no severe concomitant disease (heart failure, COPD, CABG, etc.);
  • no history of known allergies or drug intolerance;
  • informed consent

Exclusion Criteria:

  • PF diagnosis uncertain;
  • poor general status (Karnoffsky <80, ECOG > 1);
  • the presence of serious complications; see above
  • recent history of severe heart, lung, kidney or liver failure;
  • the history of allergies or drug intolerance;
  • confirmed neoplastic spread;
  • severe malnutrition requiring combined treatment (PN+EN)
  • withdrawal of consent

Sites / Locations

  • Nutrimed Medical Corporation

Outcomes

Primary Outcome Measures

The ratio of pancreatic fistula closure after 30 days is selected as the primary outcome measure

Secondary Outcome Measures

Rates of fistula and treatment-related complications, changes in quality of life

Full Information

First Posted
December 2, 2009
Last Updated
December 2, 2009
Sponsor
Jagiellonian University
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1. Study Identification

Unique Protocol Identification Number
NCT01025414
Brief Title
Enteral Nutrition in the Treatment of Pancreatic Fistulas - A Prospective Study
Acronym
FIS-1
Official Title
The Use of Enteral Nutrition in the Treatment of Pancreatic Fistulas - A Prospective, Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2009
Overall Recruitment Status
Completed
Study Start Date
July 2006 (undefined)
Primary Completion Date
October 2009 (Actual)
Study Completion Date
November 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Jagiellonian University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary objective of this study is to evaluate the effectives of enteral nutrition in the treatment of pancreatic fistulas. The ratio of pancreatic fistula closure after 30 days is selected as the primary outcome measure with the null hypothesis assuming that enteral nutrition provides better results than parenteral nutrition as far as the closure ratio, time to closure and treatment-related complications are concerned.
Detailed Description
The research into field of the role of enteral nutrition in the treatment of pancreatic fistulas is fully justified by the lower cost and complications' rate of EN compared to PN observed in clinical trials comparing enteral and parnetral route of feeding in pre- and postoperative period. Such authors as Braga, Torosian, Lewis or Sand et al. proved that use of enteral nutrition led to smaller amount of complication (especially infectious) and improved the outcome of surgery. The only method to verify the role of enteral nutrition is the prospective, randomized clinical trial. STUDY OBJECTIVES 2.1 Primary Objective The primary objective of this study is to evaluate the effectives of enteral nutrition in the treatment of pancreatic fistulas. The ratio of pancreatic fistula closure after 30 days is selected as the primary outcome measure with the null hypothesis assuming that enteral nutrition provides better results than parenteral nutrition as far as the closure ratio, time to closure and treatment-related complications are concerned. 2.2 Secondary Objectives The secondary objectives are to: determine time to fistula closure (defined as time between initiation of treatment and confirmed fistula closure), determine rates of fistula and treatment-related complications, assess changes in quality of life (QoL), determine economic costs of therapy. (for such terms as: fistula closure, time to closure see definition on page 3) For QoL assessment the EORTC QLQ - PAN26 score in Polish version (translation was approved by EORTC) will be used. Benefits of the study: the implementation of safer and less expensive conservative procedure. Basis: Costs of enteral nutrition are significantly lower than PN and EN is significantly safer than PN especially as far as infectious complications are concerned. the enhancement of indications for enteral nutrition. The confirmation of the null hypothesis allows recommending enteral nutrition as a method of choice for pancreatic fistula treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pancreatic Fistula
Keywords
pancreatic fistula

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
78 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
enteral nutrition
Other Intervention Name(s)
Peptisorb, Nutricia Ltd, Netherlands
Intervention Description
Group A - enteral feeding was started 2 to 4 hours after catheter placement via enteral tube inserted via endoscope below the Treitz's ligament into first intestinal loop (location of the tip) (Nutricial Ltd. Flocare). The initial flow rate was 10 ml/ hour, final 125 ml/ hour. Energy requirements was calculated using following rule: 0.15-0.2 gN/ kg and 130-170 kcal/ gN. Diet: Peptisorb (Nutricia Ltd.) - oligopeptide diet well tolerated by intestines
Intervention Type
Drug
Intervention Name(s)
Parenteral nutrition
Other Intervention Name(s)
intravenous feeding
Intervention Description
Parenteral nutrition was started 2 to 4 hours after venous catheter placement (standard Arrow type, the tip located 5 cm over right vestibule, the location confirmed on chest X-ray) and continued until oral diet covering at least 60% of daily caloric and protein demand. The energy requirements were calculated using following rule: 0.15-0.2 gN/ kg and 130-170 kcal/ gN. Parenteral diets: Aminoplasmal 10%, Lipofundin LCT/MCT 10 and 20%, 40% Glucose, Tracutil (microelements and trace elements), Cernevit (vitamins), electrolytes
Primary Outcome Measure Information:
Title
The ratio of pancreatic fistula closure after 30 days is selected as the primary outcome measure
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Rates of fistula and treatment-related complications, changes in quality of life
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: the presence of pancreatic fistula (PF) (verification of serum lipase concentration in drained fluid, findings on imaging modalities: endoscopic retrograde cholangiopancreatography (ERCP), helical computed tomography(hCT), magnetic reissonance imaging (MRI), ultrasonography (USG) or intraoperative surgeon's verification - any or some or all of them) good general status (Karnoffsky > 80, Eastern Cooperative Oncology Group (ECOG) scale 0 or 1; see Appendix 2); NRS and MUST evaluation - low/ medium risk patients not requiring parenteral nutrition as the essence treatment option, no PF's complication requiring special treatment present, such as intraabdominal abscess formation, pleuropneumonia, bleeding, paralytic ileus, etc. Complications will be diagnosed and treated according to generally accepted medical knowledge, standards and procedures. age below 80 and over 18; in case of neoplastic patients: no confirmed neoplastic dissemination nor distant metastases; no severe concomitant disease (heart failure, COPD, CABG, etc.); no history of known allergies or drug intolerance; informed consent Exclusion Criteria: PF diagnosis uncertain; poor general status (Karnoffsky <80, ECOG > 1); the presence of serious complications; see above recent history of severe heart, lung, kidney or liver failure; the history of allergies or drug intolerance; confirmed neoplastic spread; severe malnutrition requiring combined treatment (PN+EN) withdrawal of consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stanislaw Klek, MD PhD
Organizational Affiliation
Jagiellonian University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nutrimed Medical Corporation
City
Krakow
State/Province
Malopolska
ZIP/Postal Code
30-798
Country
Poland

12. IPD Sharing Statement

Citations:
PubMed Identifier
21439962
Citation
Klek S, Sierzega M, Turczynowski L, Szybinski P, Szczepanek K, Kulig J. Enteral and parenteral nutrition in the conservative treatment of pancreatic fistula: a randomized clinical trial. Gastroenterology. 2011 Jul;141(1):157-63, 163.e1. doi: 10.1053/j.gastro.2011.03.040. Epub 2011 Mar 24.
Results Reference
derived

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Enteral Nutrition in the Treatment of Pancreatic Fistulas - A Prospective Study

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