Evidence mapPaperPMID 33710717Full record

Trial reportDiabetes, obesity & metabolism2021

Oral semaglutide improves postprandial glucose and lipid metabolism, and delays gastric emptying, in subjects with type 2 diabetes.

Kirsten Dahl, Ashley Brooks, Firas Almazedi, Søren Tetens Hoff, Cristina Boschini, Tine A Baekdal

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetes, obesity & metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
7.9field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 74 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 2 countries.

Kirsten DahlNovo Nordisk A/S, Søborg, Denmark.ORCID 0000-0001-5063-1554
Ashley BrooksCovance Clinical Research Unit Ltd, Leeds, UK.
Firas AlmazediCovance Clinical Research Unit Ltd, Leeds, UK.
Søren Tetens HoffNovo Nordisk A/S, Søborg, Denmark.
Cristina BoschiniNovo Nordisk A/S, Søborg, Denmark.
Tine A BaekdalNovo Nordisk A/S, Søborg, Denmark.ORCID 0000-0002-1348-0352
Novo Nordisk (Denmark) · DKCovance (United Kingdom) · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo assess the effects of oral semaglutide on postprandial glucose and lipid metabolism, and gastric emptying, in subjects with type 2 diabetes (T2D). MATERIALS AND

methodsIn this randomized, double-blind, single-centre, crossover trial, subjects with T2D received once-daily oral semaglutide (escalated to 14 mg) followed by placebo, or vice versa, over two consecutive 12-week periods. Glucose and lipid metabolism, and gastric emptying (paracetamol absorption) were assessed before and after two types of standardized meals (standard and/or fat-rich) at the end of each treatment period. The primary endpoint was area under the glucose 0-5-h curve (AUC

resultsFifteen subjects were enrolled (mean age 58.2 years, HbA1c 6.9%, body weight 93.9 kg, diabetes duration 3.1 years; 13 [86.7%] males). Fasting concentrations of glucose were significantly lower, and C-peptide significantly greater, with oral semaglutide versus placebo. Postprandial glucose (AUC

conclusionOral semaglutide significantly improved fasting and postprandial glucose and lipid metabolism, and delayed gastric emptying.

Indexed as

Diabetes Mellitus, Type 2Blood GlucoseDouble-Blind MethodGastric EmptyingGlucagon-Like PeptidesGlucoseHumansHypoglycemic AgentsLipid MetabolismMaleMiddle AgedPostprandial PeriodSemaglutideBlood GlucoseGlucagon-Like PeptidesGlucoseHypoglycemic AgentsSemaglutidedyslipidaemiaGLP-1 analogueglycaemic controlincretin therapypharmacodynamicstype 2 diabetes

Identifiers

PMID33710717
PMCPMC8251575
OpenAlexW3135617910

What Socratic holds

Texttitle and abstract
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.