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Study · Randomized controlled trial · n = 211 · 2000

4 results

Does prophylactic octreotide decrease the rates of pancreatic fistula and other complications after pancreaticoduodenectomy? Results of a prospective randomized placebo-controlled trial.

Yeo CJ, Cameron JL, Lillemoe KD, Sauter PK, Coleman J, Sohn TA, Campbell KA, Choti MA

Annals of surgery1 Sept 2000Cited by 373 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study4

4 results from studies that gave the peptide. 4 results from people.

  1. 01HumanRandomized controlled trialSafety outcome

    After pancreaticoduodenectomy, fistula rates were 11% with octreotide and 9% with saline.

    In plain wordsAfter pancreatic surgery, fistula rates were 11% with octreotide and 9% with saline.

    Peptide
    Octreotide
    Outcome
    IncreasePancreatic fistula
    Study

    n = 211

    Comparator
    Saline control
    Analysis
    Primary
    Outcome group
    Adverse events · Gastrointestinal
    Studied dose
    250 microg every 8 hours · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    Pancreatic fistula rate
    11%
    octreotide arm
    Pancreatic fistula rate
    9%
    saline control arm

    Source sentences

    Summary
    The pancreatic fistula rates were 9% in the control group and 11% in the octreotide group.
    2 context sentences
    Summary · context
    Patients who gave consent were randomized to saline control versus octreotide 250 microg subcutaneously every 8 hours for 7 days, to start 1 to 2 hours before surgery.
    Summary · context
    Two hundred eleven patients underwent pancreaticoduodenectomy with pancreatic-enteric anastomosis, received appropriate saline/octreotide doses, and were available for endpoint analysis.
  2. 02HumanRandomized controlled trialSafety outcome

    After pancreaticoduodenectomy, overall complications occurred in 40% with octreotide versus 34% with saline.

    In plain wordsAfter pancreatic surgery, complications occurred in 40% with octreotide versus 34% with saline.

    Peptide
    Octreotide
    Outcome
    IncreaseOverall complications
    Study

    n = 211

    Comparator
    Saline control
    Analysis
    Primary
    Outcome group
    Adverse events · Whole body
    Studied dose
    250 microg every 8 hours · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    Overall complication rate
    40%
    octreotide arm
    Overall complication rate
    34%
    saline control arm

    Source sentences

    Summary
    The overall complication rates were 34% in the control group and 40% in the octreotide group; the in-hospital death rates were 0% versus 1%, respectively.
    2 context sentences
    Summary · context
    Patients who gave consent were randomized to saline control versus octreotide 250 microg subcutaneously every 8 hours for 7 days, to start 1 to 2 hours before surgery.
    Summary · context
    Two hundred eleven patients underwent pancreaticoduodenectomy with pancreatic-enteric anastomosis, received appropriate saline/octreotide doses, and were available for endpoint analysis.
  3. 03HumanRandomized controlled trialSafety outcome

    After pancreaticoduodenectomy, in-hospital mortality was 1% with octreotide versus 0% with saline.

    In plain wordsAfter pancreatic surgery, hospital deaths occurred in 1% with octreotide versus 0% with saline.

    Peptide
    Octreotide
    Outcome
    IncreaseIn-hospital death
    Study

    n = 211

    Comparator
    Saline control
    Analysis
    Primary
    Outcome group
    Mortality · Whole body
    Studied dose
    250 microg every 8 hours · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    In-hospital death rate
    1%
    octreotide arm
    In-hospital death rate
    0%
    saline control arm

    Source sentences

    Summary
    The overall complication rates were 34% in the control group and 40% in the octreotide group; the in-hospital death rates were 0% versus 1%, respectively.
    2 context sentences
    Summary · context
    Patients who gave consent were randomized to saline control versus octreotide 250 microg subcutaneously every 8 hours for 7 days, to start 1 to 2 hours before surgery.
    Summary · context
    Two hundred eleven patients underwent pancreaticoduodenectomy with pancreatic-enteric anastomosis, received appropriate saline/octreotide doses, and were available for endpoint analysis.
  4. 04HumanRandomized controlled trialEfficacy outcome

    After pancreaticoduodenectomy, median hospital stay was 9 days with either octreotide or saline.

    In plain wordsAfter pancreatic surgery, median hospital stay was 9 days with either octreotide or saline.

    Peptide
    Octreotide
    Outcome
    No significant changePostoperative hospital stay
    Study

    n = 211

    Comparator
    Saline control
    Analysis
    Primary
    Outcome group
    Intensive care and hospital outcomes · Whole body
    Studied dose
    250 microg every 8 hours · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    Median postoperative length of hospital stay
    9 days
    octreotide arm
    Median postoperative length of hospital stay
    9 days
    saline control arm

    Source sentences

    Summary
    The median postoperative length of hospital stay was 9 days in both groups.
    2 context sentences
    Summary · context
    Patients who gave consent were randomized to saline control versus octreotide 250 microg subcutaneously every 8 hours for 7 days, to start 1 to 2 hours before surgery.
    Summary · context
    Two hundred eleven patients underwent pancreaticoduodenectomy with pancreatic-enteric anastomosis, received appropriate saline/octreotide doses, and were available for endpoint analysis.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Registered trials2

Trials this study reports on, or that list this study as a reference. Registry data from ClinicalTrials.gov.

2 trials · 2 completed · source ClinicalTrials.gov (opens in a new tab)

CompletedNot applicableNCT02474914

Octreotide in the Prevention of Postoperative Complications After Pancreaticoduodenectomy

Mansoura Universityn = 104May 2014 to Apr 2017

Periampullary Carcinoma Resectable

Trial pageClinicalTrials.govUpdated 22 Aug 2017
CompletedPhase 4NCT01301222

Role of Octreotide in Preventing Pancreatic Fistula After Pancreaticoduodenectomy (PD) in Patients With Soft Pancreas

PVS Memorial Hospitaln = 110Sept 2010 to Feb 2015

Pancreatic Fistula

Trial pageClinicalTrials.govUpdated 24 Feb 2015

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    28 Oct 2026, 02:03 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:36 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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