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Study · Randomized controlled trial · n = 199 · 1995

6 results

Sclerotherapy with or without octreotide for acute variceal bleeding.

Besson I, Ingrand P, Person B, Boutroux D, Heresbach D, Bernard P, Hochain P, Larricq J, Gourlaouen A, Ribard D

The New England journal of medicine1 Aug 1995Cited by 164 (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 study6

6 results from studies that gave the peptide. 6 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    After sclerotherapy in cirrhosis, five-day survival without rebleeding was 85/98 with octreotide versus 72/101 with placebo (P = 0.009, difference CI 4–27 percent).

    In plain wordsIn cirrhotic patients after sclerotherapy, octreotide increased survival without rebleeding versus placebo.

    Peptide
    Octreotide
    Outcome
    IncreaseSurvival without rebleeding at five days
    Study

    n = 199

    Comparator
    Sclerotherapy plus placebo
    Analysis
    Primary
    Outcome group
    Gastrointestinal protection · Gastrointestinal
    Studied dose
    25 micrograms per hour · continuous infusion · five daysAs given in this study (human).

    Measurements

    Survival without rebleeding at 5 days
    87 percent
    octreotide group, 85 of 98 patients
    Survival without rebleeding at 5 days
    71 percent
    placebo group, 72 of 101 patients
    95 percent confidence interval for the difference
    4 to 27 percent
    octreotide minus placebo
    P value
    0.009
    survival without rebleeding

    Source sentences

    Summary
    After five days, the proportion of patients who had survived without rebleeding was higher in the octreotide group (85 of 98 patients, or 87 percent) than in the placebo group (72 of 101, or 71 percent; 95 percent confidence interval for the difference, 4 to 27 percent; P = 0.009).
    2 context sentences
    Summary · context
    In a double-blind, prospective trial, 199 patients with cirrhosis and acute variceal bleeding who underwent emergency sclerotherapy were randomly assigned to receive a continuous infusion of octreotide (25 micrograms per hour) or placebo for five days.
    Summary · context
    The primary outcome measure was survival without rebleeding five days after sclerotherapy.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In cirrhotic patients after sclerotherapy, octreotide reduced transfusion to 1.2 units (range 0 to 7) versus 2.0 (0 to 10) with placebo (P = 0.006).

    In plain wordsIn cirrhotic patients after sclerotherapy, octreotide reduced blood transfusion needs versus placebo during the first 24 hours.

    Peptide
    Octreotide
    Outcome
    DecreaseBlood transfusion in first 24 hours
    Study

    n = 199

    Comparator
    Sclerotherapy plus placebo
    Outcome group
    Gastrointestinal protection · Gastrointestinal
    Studied dose
    25 micrograms per hour · continuous infusion · five daysAs given in this study (human).

    Measurements

    Blood units transfused in first 24 hours
    1.2 units
    octreotide group, range 0 to 7
    Blood units transfused in first 24 hours
    2 units
    placebo group, range 0 to 10
    Range of units transfused
    0 to 7 units
    octreotide group
    Range of units transfused
    0 to 10 units
    placebo group
    P value
    0.006
    transfusion in first 24 hours

    Source sentences

    Summary
    The mean number of units of blood transfused within the first 24 hours after sclerotherapy was lower in the octreotide group (1.2 units; range, 0 to 7) than in the placebo group (2.0 units; range, 0 to 10; P = 0.006).
    1 context sentence
    Summary · context
    In a double-blind, prospective trial, 199 patients with cirrhosis and acute variceal bleeding who underwent emergency sclerotherapy were randomly assigned to receive a continuous infusion of octreotide (25 micrograms per hour) or placebo for five days.
  3. 03HumanRandomized controlled trialEfficacy outcome

    In cirrhotic patients after sclerotherapy, treatment assignment independently predicted survival without rebleeding (P = 0.003), favoring octreotide.

    In plain wordsIn cirrhotic patients after sclerotherapy, octreotide assignment was independently linked to survival without rebleeding versus placebo.

    Peptide
    Octreotide
    Outcome
    IncreaseTreatment assignment association with survival without rebleeding
    Study

    n = 199

    Comparator
    Sclerotherapy plus placebo
    Outcome group
    Gastrointestinal protection · Gastrointestinal
    Studied dose
    25 micrograms per hour · continuous infusion · five daysAs given in this study (human).

    Measurements

    P value
    0.003
    treatment assignment association with survival without rebleeding

    Source sentences

    Summary
    A logistic-regression analysis showed that the treatment assignment (P = 0.003) and the number of blood units transfused before any other treatment was undertaken (P = 0.002) were the only two variables independently associated with survival without rebleeding.
    2 context sentences
    Summary · context
    After five days, the proportion of patients who had survived without rebleeding was higher in the octreotide group (85 of 98 patients, or 87 percent) than in the placebo group (72 of 101, or 71 percent; 95 percent confidence interval for the difference, 4 to 27 percent; P = 0.009).
    Summary · context
    In a double-blind, prospective trial, 199 patients with cirrhosis and acute variceal bleeding who underwent emergency sclerotherapy were randomly assigned to receive a continuous infusion of octreotide (25 micrograms per hour) or placebo for five days.
  4. 04HumanRandomized controlled trialEfficacy outcome

    In cirrhotic patients after sclerotherapy, adjusted treatment failure odds were higher with placebo than octreotide: 3.3 (95 percent CI 1.5 to 7.3).

    In plain wordsIn cirrhotic patients after sclerotherapy, adjusted treatment failure odds were lower with octreotide than placebo.

    Peptide
    Octreotide
    Outcome
    DecreaseAdjusted treatment failure odds
    Study

    n = 199

    Comparator
    Sclerotherapy plus placebo
    Outcome group
    Gastrointestinal protection · Gastrointestinal
    Studied dose
    25 micrograms per hour · continuous infusion · five daysAs given in this study (human).

    Measurements

    Adjusted odds ratio for treatment failure
    3.3
    placebo versus octreotide
    95 percent confidence interval for odds ratio
    1.5 to 7.3
    placebo versus octreotide

    Source sentences

    Summary
    After adjustment for base-line differences between the two groups, the odds ratio for treatment failure in the placebo group, as compared with the octreotide group, was 3.3 (95 percent confidence interval, 1.5 to 7.3).
    1 context sentence
    Summary · context
    In a double-blind, prospective trial, 199 patients with cirrhosis and acute variceal bleeding who underwent emergency sclerotherapy were randomly assigned to receive a continuous infusion of octreotide (25 micrograms per hour) or placebo for five days.
  5. 05HumanRandomized controlled trialEfficacy outcome

    In cirrhotic patients after sclerotherapy, 15-day cumulative survival was 88 +/- 12 percent in both octreotide and placebo groups.

    In plain wordsIn cirrhotic patients after sclerotherapy, survival at 15 days was the same with octreotide and placebo.

    Peptide
    Octreotide
    Outcome
    No significant change15-day cumulative survival
    Study

    n = 199

    Comparator
    Sclerotherapy plus placebo
    Outcome group
    Mortality · Gastrointestinal
    Studied dose
    25 micrograms per hour · continuous infusion · five daysAs given in this study (human).

    Measurements

    15-day cumulative survival (Kaplan-Meier)
    88 percent
    both groups
    SD of 15-day cumulative survival
    12 percent
    both groups

    Source sentences

    Summary
    The mean (+/- SD) 15-day cumulative survival rate (estimated by the Kaplan-Meier method) was 88 +/- 12 percent in both groups.
    1 context sentence
    Summary · context
    In a double-blind, prospective trial, 199 patients with cirrhosis and acute variceal bleeding who underwent emergency sclerotherapy were randomly assigned to receive a continuous infusion of octreotide (25 micrograms per hour) or placebo for five days.
  6. 06HumanRandomized controlled trialSafety outcome

    In cirrhotic patients after sclerotherapy, side effects were minor and had similar incidence with octreotide and placebo.

    In plain wordsIn cirrhotic patients after sclerotherapy, minor side effects occurred at similar rates with octreotide and placebo.

    Peptide
    Octreotide
    Outcome
    No significant changeSide effects
    Study

    n = 199

    Comparator
    Sclerotherapy plus placebo
    Outcome group
    Adverse events · Whole body
    Studied dose
    25 micrograms per hour · continuous infusion · five daysAs given in this study (human).

    Source sentences

    Summary
    Side effects were minor, and their incidence was similar in the two groups.
    1 context sentence
    Summary · context
    In a double-blind, prospective trial, 199 patients with cirrhosis and acute variceal bleeding who underwent emergency sclerotherapy were randomly assigned to receive a continuous infusion of octreotide (25 micrograms per hour) or placebo for five days.

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

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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