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Completed

NCT Number: NCT01025414

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

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.

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Key information

Age range

18 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Nutrimed Medical Corporation

Krakow, Malopolska, 30-798, Poland

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

enteral nutrition

Drug

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

Other names: Peptisorb, Nutricia Ltd, Netherlands

Parenteral Nutrition

Drug

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

Other names: intravenous feeding

Primary outcomes

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

    Time frame: 30 days

Secondary outcomes

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

    Time frame: 30 days

Sponsors and collaborators

Lead sponsor

Jagiellonian University

Other

Registry information

Official study title

The Use of Enteral Nutrition in the Treatment of Pancreatic Fistulas - A Prospective, Randomized Clinical Trial

Acronym: FIS-1

Important dates

Study start
2006
Primary completion
2009
Study completion
2009
First posted
Dec 3, 2009
Registry last updated
Dec 3, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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