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Trial · Interventional

CompletedNot applicableRegistry data

The Impact of Lixisenatide on Postprandial Glucose Tolerance in Pancreatectomised Subjects

Short name Px-Lixi

Overview

Status
Completed
Phase
Not applicable
Enrollment
24 participants (actual)
Sponsor
University Hospital, Gentofte, Copenhagen · Other
Design
Randomized · Double masking
Countries
Not stated
Start
Aug 2015
Primary completion
Jul 2016
Completion
Jul 2016
First posted
28 Dec 2015 (estimated)
Last update posted
7 May 2020
Conditions
Diabetes After Total Pancreatectomy

Timeline

1 trial · 1 completed

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
201520162017
  1. N/A

    Px-Lixi

    NCT02640118

    Aug 2015 to Jul 2016

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

Postprandial glucose (PPG) excursions are not only determined by insulin-mediated glucose disposal and endogenous glucose production (regulated by insulin and glucagon); also the rate of gastric emptying constitutes an important determinant of PPG levels 1. The short-acting glucagon-like peptide-1 (GLP-1) receptor agonist lixisenatide is used in the treatment of type 2 diabetes. It increases glucose-dependent insulin secretion, suppresses glucagon secretion and reduces gastric emptying of meals 2. These three mechanisms most likely constitute the weightiest mechanisms behind the potent impact of lixisenatide on exaggerated PPG excursions in patients with type 2 diabetes - which often are normalised during lixisenatide treatment 3. However, the separate impact of lixisenatide-induced reduction of gastric emptying (independently of the pancreatic effects) has been difficult to determine. Importantly, treatment with lixisenatide also decreases appetite and food intake and may, like native GLP-1, increase energy expenditure 4. So far an exact demarcation of the pancreatic and extrapancreatic effects of lixisenatide in humans remains to be established. The present project serves to determine whether effects of lixisenatide on gastric emptying, appetite, food intake and resting energy expenditure are dependent on the endocrine pancreas. The study is a randomised, placebo-controlled, double-blinded, cross-over study. 12 healthy persons and 12 pancreatectomized patients (i.e. patients who have had their pancreata removed due to pancreatic cancer or severe chronic pancreatitis) will be subjected to two experimental days on which they will undergo a liquid meal test followed by a fasting period and finished off with an ad libitum meal with lixisenatide and placebo, respectively.

Interventions

  • LixisenatideDrug
  • Lixisenatide-PlaceboDrug
  • Standardized liquid mealOther

Arms4

  • Active comparator

    Pancreatectomised + Lixisenatide

    During the experimental day the patient will ingest a standardized liquid meal (200 ml containing 1,650 kJ (394 kcal): carbohydrate 50%, protein 15%, fat 35%, consisting of glucose (48.4 g + 1.6 g \[U-13C6\]-glucose), rapeseed oil (14.1 g), whey protein (15.2 g) and 1.5 g paracetamol). Before the meal a Lixisenatide-injection will be given subcutaneously

  • Placebo comparator

    Pancreatectomized + lixisenatide-placebo

    During the experimental day the patient will ingest a standardized liquid meal (200 ml containing 1,650 kJ (394 kcal): carbohydrate 50%, protein 15%, fat 35%, consisting of glucose (48.4 g + 1.6 g \[U-13C6\]-glucose), rapeseed oil (14.1 g), whey protein (15.2 g) and 1.5 g paracetamol). Before the meal a placebo-injection will be given subcutaneously.

  • Active comparator

    Healthy + Lixisenatide

    During the experimental day the subject will ingest a standardized liquid meal (200 ml containing 1,650 kJ (394 kcal): carbohydrate 50%, protein 15%, fat 35%, consisting of glucose (48.4 g + 1.6 g \[U-13C6\]-glucose), rapeseed oil (14.1 g), whey protein (15.2 g) and 1.5 g paracetamol). Before the meal a Lixisenatide-injection will be given subcutaneously

  • Placebo comparator

    Healthy + lixisenatide-placebo

    During the experimental day the subject will ingest a standardized liquid meal (200 ml containing 1,650 kJ (394 kcal): carbohydrate 50%, protein 15%, fat 35%, consisting of glucose (48.4 g + 1.6 g \[U-13C6\]-glucose), rapeseed oil (14.1 g), whey protein (15.2 g) and 1.5 g paracetamol). Before the meal a placebo-injection will be given subcutaneously

Primary outcomes1

Outcomes the sponsor listed as primary.

  1. PPG excursions measured as incremental area under curve (iAUC)

    Time frame · -120,-45,-30,-15,0,5,10,15,20,25,30,40,50,60,70,80,90,105,120,135,150,180 minutes

Secondary outcomes(6)
  1. differences in gastric emptying, measurement of s-paracetamol

    Time frame · -30,-15,0,5,10,15,20,25,30,40,50,60,70,80,90,105,120,135,150,180 minutes

    Registry description

    measurement of time to peak and incremental area under the curve (iAUC)

  2. food intake and appetite

    Time frame · at time 0,30,60,90,120,150,180 minutes

    Registry description

    assessed by a visual analogue scale (VAS)

  3. resting energy expenditure (REE)

    Time frame · -90,30,150 minutes

    Registry description

    measured by calorimetry

  4. p-glucose mmol/L

    Time frame · -30,-15,0,5,10,15,20,25,30,40,50,60,70,80,90,105,120,135,150,180 minutes

  5. p-C-peptide pmol/l

    Time frame · -30,-15,0,5,10,15,20,25,30,40,50,60,70,80,90,105,120,135,150,180 minutes

  6. glucagon, gastrin, cholecystokinin, GIP, GLP-1, oxyntomodulin

    Time frame · -30,-15,0,5,10,15,20,25,30,40,50,60,70,80,90,105,120,135,150,180 minutes

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

No results are posted for this trial.

Completed trials do not always post results.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies1

Studies that cite this trial.

Studies with results

1 study on this page

Indexing hint: Randomized controlled trial · 2020

11 results

The GLP-1 receptor agonist lixisenatide reduces postprandial glucose in patients with diabetes secondary to total pancreatectomy: a randomised, placebo-controlled, double-blinded crossover trial.

Juel et al. 2020Diabetologiacited by 19

PMID 32394228DOI 10.1007/s00125-020-05158-9PUB-32394228

Rights unknown11 results

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years up to 80 Years
Healthy volunteers
Accepted
Inclusion and exclusion criteria, as posted
Inclusion criteria Pancreatectomised patients * Caucasians above 18 years of age who have undergone total pancreatectomy * Normal haemoglobin * Informed consent Healthy subjects * Normal fasting plasma glucose (FPG) and normal HbA1C (according to the World Health Organization (WHO) criteria) * Normal haemoglobin * Age above 18 years * Informed consent Exclusion criteria Pancreatectomised patients * Inflammatory bowel disease * Operation within the last 3 months * Ongoing chemotherapy or chemotherapy within the last 3 months * Ostomy * Nephropathy (serum creatinine \>150 µM and/or albuminuria) * Severe liver disease (serum alanine aminotransferase (ALAT) and/or serum aspartate aminotransferase (ASAT) \>3×normal values) * Pregnancy and/or breastfeeding * Age above 80 years * Any condition that the investigator feels would interfere with trial participation Healthy subjects * Diabetes mellitus (DM) * Prediabetes (impaired glucose tolerance and/or impaired FPG) * First degree relatives with DM * Inflammatory bowel disease * Intestinal resection and/or ostomy * Nephropathy (serum creatinine \>150 µM and/or albuminuria * Liver disease (ALAT and/or serum ASAT \>2×normal values) * Pregnancy and/or breastfeeding * Age above 80 years * Any condition that the investigator feels would interfere with trial participation

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