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Study · Randomized controlled trial · n = 17 · 2008

8 results

Effect of exenatide on gastric emptying and relationship to postprandial glycemia in type 2 diabetes.

Linnebjerg H, Park S, Kothare PA, Trautmann ME, Mace K, Fineman M, Wilding I, Nauck M, Horowitz M

Regulatory peptides16 Jul 2008Cited by 206 (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 study8

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

  1. 01HumanRandomized controlled trialMechanism

    In subjects with type 2 diabetes, exenatide at the lower dose prolonged solid gastric emptying half-time versus placebo.

    In plain wordsIn people with diabetes, lower-dose exenatide slowed solid stomach emptying compared with placebo.

    Outcome
    IncreaseSolid gastric emptying T50, lower dose
    Study

    n = 17

    Comparator
    Placebo
    Outcome group
    Gastrointestinal motility · Gastrointestinal
    Studied dose
    5 microg BID · subcutaneous · 5 daysAs given in this study (human).

    Measurements

    Solid T50
    111 min
    5 microg exenatide
    Solid T50
    60 min
    placebo

    Source sentences

    Summary
    Exenatide slowed GE of both solid and liquid meal components [solid (T(50)(90% confidence interval [CI]); placebo, 60(50-70) min; 5 microg exenatide, 111(94-132) min; 10 microg exenatide, 169(143-201) min; both P<0.01);
    1 context sentence
    Summary · context
    Seventeen subjects with type 2 diabetes participated in a randomized, single-blind, 3-period, crossover study. In each 5-day period, 5 or 10 microg exenatide or placebo was administered subcutaneously BID. Oral antidiabetic treatments were continued.
  2. 02HumanRandomized controlled trialMechanism

    In subjects with type 2 diabetes, exenatide at the higher dose prolonged solid gastric emptying half-time versus placebo.

    In plain wordsIn people with diabetes, higher-dose exenatide slowed solid stomach emptying compared with placebo.

    Outcome
    IncreaseSolid gastric emptying T50, higher dose
    Study

    n = 17

    Comparator
    Placebo
    Outcome group
    Gastrointestinal motility · Gastrointestinal
    Studied dose
    10 microg BID · subcutaneous · 5 daysAs given in this study (human).

    Measurements

    Solid T50
    169 min
    10 microg exenatide
    Solid T50
    60 min
    placebo

    Source sentences

    Summary
    Exenatide slowed GE of both solid and liquid meal components [solid (T(50)(90% confidence interval [CI]); placebo, 60(50-70) min; 5 microg exenatide, 111(94-132) min; 10 microg exenatide, 169(143-201) min; both P<0.01);
    1 context sentence
    Summary · context
    Seventeen subjects with type 2 diabetes participated in a randomized, single-blind, 3-period, crossover study. In each 5-day period, 5 or 10 microg exenatide or placebo was administered subcutaneously BID. Oral antidiabetic treatments were continued.
  3. 03HumanRandomized controlled trialMechanism

    In subjects with type 2 diabetes, exenatide at the lower dose prolonged liquid gastric emptying half-time versus placebo.

    In plain wordsIn people with diabetes, lower-dose exenatide slowed liquid stomach emptying compared with placebo.

    Outcome
    IncreaseLiquid gastric emptying T50, lower dose
    Study

    n = 17

    Comparator
    Placebo
    Outcome group
    Gastrointestinal motility · Gastrointestinal
    Studied dose
    5 microg BID · subcutaneous · 5 daysAs given in this study (human).

    Measurements

    Liquid T50
    87 min
    5 microg exenatide
    Liquid T50
    34 min
    placebo

    Source sentences

    Summary
    liquid (T(50)(90% CI), placebo, 34(25-46) min; 5 microg exenatide, 87(65-117) min; 10 microg exenatide, 114(85-154) min; both P<0.01)].
    1 context sentence
    Summary · context
    Seventeen subjects with type 2 diabetes participated in a randomized, single-blind, 3-period, crossover study. In each 5-day period, 5 or 10 microg exenatide or placebo was administered subcutaneously BID. Oral antidiabetic treatments were continued.
  4. 04HumanRandomized controlled trialMechanism

    In subjects with type 2 diabetes, exenatide at the higher dose prolonged liquid gastric emptying half-time versus placebo.

    In plain wordsIn people with diabetes, higher-dose exenatide slowed liquid stomach emptying compared with placebo.

    Outcome
    IncreaseLiquid gastric emptying T50, higher dose
    Study

    n = 17

    Comparator
    Placebo
    Outcome group
    Gastrointestinal motility · Gastrointestinal
    Studied dose
    10 microg BID · subcutaneous · 5 daysAs given in this study (human).

    Measurements

    Liquid T50
    114 min
    10 microg exenatide
    Liquid T50
    34 min
    placebo

    Source sentences

    Summary
    liquid (T(50)(90% CI), placebo, 34(25-46) min; 5 microg exenatide, 87(65-117) min; 10 microg exenatide, 114(85-154) min; both P<0.01)].
    1 context sentence
    Summary · context
    Seventeen subjects with type 2 diabetes participated in a randomized, single-blind, 3-period, crossover study. In each 5-day period, 5 or 10 microg exenatide or placebo was administered subcutaneously BID. Oral antidiabetic treatments were continued.
  5. 05HumanRandomized controlled trialMechanism

    In subjects with type 2 diabetes, exenatide reduced postprandial glucose AUC by 69-76% compared with placebo.

    In plain wordsIn people with diabetes, exenatide reduced post-meal glucose exposure compared with placebo.

    Outcome
    DecreasePostprandial glucose AUC
    Study

    n = 17

    Comparator
    Placebo
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5 or 10 microg BID · subcutaneous · 5 daysAs given in this study (human).

    Measurements

    Postprandial glucose AUC reduction
    69 to 76%
    exenatide versus placebo

    Source sentences

    Summary
    Exenatide reduced postprandial glucose (area under the curve [AUC((0-6 h))]) by 69-76% and peak insulin (C(max)) by 84-86% compared with placebo.
    1 context sentence
    Summary · context
    Seventeen subjects with type 2 diabetes participated in a randomized, single-blind, 3-period, crossover study. In each 5-day period, 5 or 10 microg exenatide or placebo was administered subcutaneously BID. Oral antidiabetic treatments were continued.
  6. 06HumanRandomized controlled trialMechanism

    In subjects with type 2 diabetes, exenatide reduced peak insulin by 84-86% compared with placebo.

    In plain wordsIn people with diabetes, exenatide reduced peak insulin compared with placebo.

    Outcome
    DecreasePeak insulin concentration
    Study

    n = 17

    Comparator
    Placebo
    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    5 or 10 microg BID · subcutaneous · 5 daysAs given in this study (human).

    Measurements

    Peak insulin reduction
    84 to 86%
    exenatide versus placebo

    Source sentences

    Summary
    Exenatide reduced postprandial glucose (area under the curve [AUC((0-6 h))]) by 69-76% and peak insulin (C(max)) by 84-86% compared with placebo.
    1 context sentence
    Summary · context
    Seventeen subjects with type 2 diabetes participated in a randomized, single-blind, 3-period, crossover study. In each 5-day period, 5 or 10 microg exenatide or placebo was administered subcutaneously BID. Oral antidiabetic treatments were continued.

Studies that did not test the peptide alone2

In this study, Exenatide (exendin-4) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Exenatide (exendin-4).

  1. 07HumanNot a test of Exenatide (exendin-4) aloneObservational studyMechanism

    In subjects with type 2 diabetes, gastric emptying did not differ between those with and without cardiac autonomic neuropathy.

    In plain wordsIn people with diabetes, stomach emptying did not differ between those with and without cardiac autonomic neuropathy.

    Outcome
    No significant changeGastric emptying by autonomic neuropathy
    Study

    n = 17

    Comparator
    Subjects without cardiac autonomic neuropathy
    Outcome group
    Gastrointestinal motility · Gastrointestinal

    Source sentences

    Summary
    GE was not different between subjects with cardiac autonomic neuropathy (n=7), compared with those without (n=10) (P>/=0.68).
    1 context sentence
    Summary · context
    Seventeen subjects with type 2 diabetes participated in a randomized, single-blind, 3-period, crossover study. In each 5-day period, 5 or 10 microg exenatide or placebo was administered subcutaneously BID. Oral antidiabetic treatments were continued.

    In this study, Exenatide (exendin-4) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Exenatide (exendin-4).

  2. 08HumanNot a test of Exenatide (exendin-4) aloneObservational studyMechanism

    In subjects with type 2 diabetes, postprandial glucose rise was inversely related to solid gastric emptying half-time.

    In plain wordsIn people with diabetes, slower solid stomach emptying was linked to a smaller post-meal glucose rise.

    Outcome
    DecreaseGlucose rise association with gastric emptying
    Study

    n = 17

    Outcome group
    Glycemic control · Metabolic and weight

    Measurements

    Correlation coefficient
    −0.49 r
    glucose AUC and solid T50

    Source sentences

    Summary
    There was an inverse relationship between the postprandial rise in glucose (AUC((0-3 h))) and GE (solid T(50), r=-0.49, P<0.001).
    1 context sentence
    Summary · context
    Seventeen subjects with type 2 diabetes participated in a randomized, single-blind, 3-period, crossover study. In each 5-day period, 5 or 10 microg exenatide or placebo was administered subcutaneously BID. Oral antidiabetic treatments were continued.

    In this study, Exenatide (exendin-4) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Exenatide (exendin-4).

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

    22 Oct 2026, 02:26 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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