Evidence map›Paper›PMID 38365744›Full record

ArticleTrials2024

Obesity Treatments to Improve Type 1 Diabetes (OTID): a randomized controlled trial of the combination of glucagon-like peptide 1 analogues and sodium-glucose cotransporter 2 inhibitors-protocol for Obesity Treatments to Improve Type 1 Diabetes (the OTID trial).

Ebaa Al-Ozairi, Kavita Narula, Alexander D Miras, Etab Taghadom, Abeer El Samad, Jumana Al Kandari, Anas Alyosef, Anant Mashankar, Werd Al-Najim, Carel W le Roux

Registry-linked trialOpen access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT05390307. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 22% 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.

NCT05390307 nacompleted

Obesity Treatment to Improve Diabetes

Ran2023Enrolled60Registered outcomes7Posted comparisons0ConditionsType 1 DiabetesArmsdapagliflozin, Liraglutide or Semaglutide / Dapagliflozin, Liraglutide or Semaglutide / Dapagliflozin plus intensive weight loss nutrition, Liraglutide / Semaglutide, Usual Care
Open the trial in the graph
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 5 institutions in 3 countries.

Ebaa Al-OzairiDasman Diabetes Institute, Kuwait City, Kuwait.
Kavita NarulaDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK. k.narula@nhs.net.ORCID http://orcid.org/0000-0002-7453-9039
Alexander D MirasDepartment of Metabolism, Digestion and Reproduction, Imperial College London, London, UK.
Etab TaghadomDasman Diabetes Institute, Kuwait City, Kuwait.
Abeer El SamadDasman Diabetes Institute, Kuwait City, Kuwait.
Jumana Al KandariDasman Diabetes Institute, Kuwait City, Kuwait.
Anas AlyosefAmiri Hospital, Ministry of Health, Kuwait City, Kuwait.
Anant MashankarDasman Diabetes Institute, Kuwait City, Kuwait.
Werd Al-NajimSchool of Medicine, Ulster University, Coleraine, UK.
Carel W le RouxSchool of Medicine, Ulster University, Coleraine, UK.
Amiri Hospital · KWDasman Diabetes Institute · KWUniversity College Dublin · IEImperial College London · GBUniversity of Ulster · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe guidelines of the American Diabetes Association and European Association for the Study of Diabetes suggest that patients with obesity type 2 diabetics and chronic kidney disease need either glucagon-like peptide 1 receptor analogues or sodium-glucose cotransporter-2 inhibitors. If neither achieve metabolic control, then the recommendation is to combine both drugs. The evidence base for combining glucagon-like peptide 1 receptor analogues and sodium-glucose cotransporter-2 inhibitors is not well researched, and hence, the impact of the guidelines is limited. The aim of this randomized controlled trial is to test the impact of the combination of glucagon-like peptide 1 receptor analogues/sodium-glucose cotransporter-2 inhibitors on body weight and kidney damage, in patients with type 1 diabetes and chronic kidney disease. In addition, we will explore the associated changes in the metabolic pathways with each of the treatments used in this randomized controlled trial.

methodsIn this 6-month randomized control trial, 60 participants aged between 21 and 65 years, with a body mass index above 25 kg/m DISCUSSION: The present randomized controlled trial aims to investigate the impact of the combination of glucagon-like peptide 1 receptor analogues and sodium-glucose cotransporter-2 inhibitors on body weight and kidney damage in patients with type 1 diabetes mellitus and chronic kidney disease, as well as exploring the associated changes in the metabolic pathways with each of the treatments used. This study addresses the current gap in the evidence base regarding the combination of these two drugs, which is particularly relevant given the American Diabetes Association and European Association for the Study of Diabetes guidelines recommending their combined use for patients with obesity, type 2 diabetes, and chronic kidney disease who do not achieve metabolic control with either drug alone.

trial registrationClinicalTrials.gov Identifier: NCT05390307 Trial registration date - 25th May 2022.

Indexed as

Diabetes Mellitus, Type 1Diabetes Mellitus, Type 2Renal Insufficiency, ChronicSodium-Glucose Transporter 2 InhibitorsAdultAgedGlucagon-Like Peptide 1GlucoseHumansHypoglycemic AgentsMiddle AgedObesityRandomized Controlled Trials as TopicSodiumYoung AdultGlucagon-Like Peptide 1GlucoseHypoglycemic AgentsSodiumSodium-Glucose Transporter 2 InhibitorsGlucagon-like peptide 1 receptor analogueObesityRandomized controlled trialSodium-glucose cotransporter 2 inhibitorType 1 diabetes

Identifiers

PMID38365744
PMCPMC10874012
OpenAlexW4391885311

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Registered trials

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 OpenQuestion graph.