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Trial · Observational

CompletedPhase not statedRegistry data

SEMAGLUTIDE VERSUS GLP-1 RECEPTOR AGONISTS. EFFECTIVENESS , SAFETY AND QUALITY OF LIFE IN PATIENTS WITH DIABETES MELLITUS 2. OBSERVATIONAL, PROSPECTIVE AND MULTICENTER STUDY. SEVERAL STUDY.

Short name SEVERAL

This trial does not test a peptide that PepBank tracks.

  • Names Dulaglutide (Trulicity), does not test it. It appears in the description.
  • Names Exenatide (exendin-4), does not test it. It appears in the description.
  • Names Liraglutide, does not test it. It appears in the description.
  • Names Lixisenatide, does not test it. It appears in the description.
  • Names Semaglutide, does not test it. It appears in the title.

Overview

Status
Completed
Phase
Phase not stated
Enrollment
140 participants (actual)
Sponsor
Jose Seijas Amigo · Other
Design
Not stated
Countries
1 country

Spain

Start
1 Feb 2022
Primary completion
15 Nov 2023
Completion
1 Jan 2024
First posted
29 Nov 2021
Last update posted
28 Feb 2024
Conditions
Weight Loss · Diabetes Mellitus, Type 2 · Quality of Life · Safety Issues

Timeline

1 trial · 1 completed

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
2022202320242025
  1. Ph –

    SEVERAL

    NCT05136287

    1 Feb 2022 to 1 Jan 2024

Registry summary

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

Introduction: GLP-1 receptor agonists (aGLP1) act increasing pancreatic insulin secretion in response to the glucose, they reduce glucagon secretion and reduce appetite by acting in the central level. Several aGLP1 were approved through different clinical trials where they showed efficacy in the glycemic control and reduction in cardiovascular events. They also showed weight loss in different clinical trials with patients with diabetes mellitus 2 (DM2) and also in specific clinical trial where the weight loss was the primary endpoint (STEP study). Objective: The objective is to evaluate and compare the weight loss in patients with DM2 treated with the different aGLP1 for the first time. Secondary endpoints are HbA1c reduction, changes in quality of life and physical activity and the safety of these drugs. Design: It is a postauthorization, multicenter, non-randomized and prospective study. Patients that will start treatment for the first time with aGLP1 will be recruited in 10 primary care centers in SERGAS Galician Hospitals for a period of 6 months and 44 weeks of follow-up. The primary endpoint will be to evaluate the wight loss with the different aGLP1 and the secondary endpoint will be HbA1c reduction, changes in the quality of life through the EuroQol-5D and changes physical activity through the SF-12 questionnaire, and also the safety of these drugs. The sample size will be of 360 patients. Statistical analysis: Previous studies showed efficacy in weight loss with semaglutide about (3,6-4,9 kg), while with other aGLP1 the weight loss was smaller , about (0,86-2,96 kg). Based in these data and with a 5% of significance level, a weight loss average in the aGLP1 group of 2,5 kg, average in semaglutide group of 4,2 kg, and combination deviation of 3,0kg, including 360 subjects we will have a statistical power above 90% to detect differences through T-test for independent samples. The justification of this simple size was performed with the statistical software SPSS 3.0 Conclusions: The SEVERAL study will try to provide information about weight loss efficacy, changes in quality of life, physical activity and safety of the aGLP1in patients with DM2 that start treatment with these drugs in the real life (Real-World Evidence)

Interventions

  • GLP-1 receptor agonistDrug

Arms1

  • Other

    Diabetes mellitus 2 patients with obesity

    Patients that meet criteria to start treatment with GLP-1 receptor agonists (dulaglutide; exenatide; liraglutide; lixisenatide )

Primary outcomes3

Outcomes the sponsor listed as primary.

  1. Weight loss

    Time frame · 11 months

    Registry description

    The primary outcome will be by assesment of % weight loss

  2. Weight loss

    Time frame · 11 months

    Registry description

    Assesment the weiht loss by reduction in Kg

  3. Weight loss

    Time frame · 11 months

    Registry description

    Assesment of changes in BMI ( weight (Kg) and height (cm) will be combined to report BMI in kg/m\^2)

Secondary outcomes(4)
  1. HbA1c values

    Time frame · 11 months

    Registry description

    HbA1c changes will be assessed during the study by routine sample tests (%)

  2. Changes in Quality of life

    Time frame · 11 months

    Registry description

    By using the questionnaire called EuroQol EQ-5D-3L assessment. It has 2 parts, the first one has 5 questions with 3 possible answers (5 dimensions and 3 levels), so each health status has a rate called EVA from 1,0000 (the highest value) to - 0,5095 (the worst health status). The second part is a visual self-assessment between 0 (the worst health status) and 100 (the best health status). https://euroqol.org/

  3. Changes in Physical Activity

    Time frame · 11 months

    Registry description

    By using the questionnaire called EuroQol SF-12 assessment.For each of the 8 dimensions, the items are coded, added and transformed on a scale that ranges from 0 (the worst health status for that dimension) to 100 (the best health status).

  4. Number of participants experiencing adverse events

    Time frame · 11 months

    Registry description

    Gastrointestinal events; hypoglycemia; pancreatitis; fatigue; ijection reactions; Diabetic retinopathy; cardiac events and other possible events

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

Studies9

Studies that cite this trial.

Studies with results

5 studies on this page

Indexing hint: Observational study · 2025

9 results

Effects of GLP-1 agonists on 10-year cardiovascular risk reduction in primary prevention: A 44-week open label prospective study.

Seijas-Amigo et al. 2025Diabetes & metabolic syndromecited by 1

PMID 41129847DOI 10.1016/j.dsx.2025.103312PUB-41129847

Full text at the publisher9 results

Indexing hint: Randomized controlled trial · 2021

10 results

Once-Weekly Semaglutide in Adults with Overweight or Obesity.

Wilding et al. 2021The New England journal of medicinecited by 3,862

PMID 33567185DOI 10.1056/nejmoa2032183PUB-33567185

Full text at the publisher10 results

Indexing hint: Randomized controlled trial · 2019

3 results

Dulaglutide and cardiovascular outcomes in type 2 diabetes (REWIND): a double-blind, randomised placebo-controlled trial.

Gerstein et al. 2019Lancet (London, England)cited by 2,264

PMID 31189511DOI 10.1016/s0140-6736(19)31149-3PUB-31189511

Full text at the publisher3 results

Indexing hint: Randomized controlled trial · 2018

21 results

Semaglutide versus dulaglutide once weekly in patients with type 2 diabetes (SUSTAIN 7): a randomised, open-label, phase 3b trial.

Pratley et al. 2018The lancet. Diabetes & endocrinologycited by 614

PMID 29397376DOI 10.1016/s2213-8587(18)30024-xPUB-29397376

Full text at the publisher21 results

Indexing hint: Randomized controlled trial · 2016

8 results

Liraglutide and Cardiovascular Outcomes in Type 2 Diabetes.

Marso et al. 2016The New England journal of medicinecited by 5,535

PMID 27295427PMC4985288DOI 10.1056/nejmoa1603827PUB-27295427

Rights unknown8 results

More studies

4 studies on this page

PubMed tag: none · 2026

Corrected

Real-world Impact of GLP-1 Receptor Agonists on Health-related Quality of Life in Type 2 Diabetes and Obesity (SEVERAL Study).

Seijas-Amigo et al. 2026Clinical therapeutics

PMID 42103575DOI 10.1016/j.clinthera.2026.03.012PUB-42103575

Full text at the publisher

PubMed tag: none · 2022

Semaglutide versus GLP-1 agonists. Effectiveness, safety, and quality of life in patients with diabetes mellitus 2. The SEVERAL study.

Seijas-Amigo et al. 2022Farmacia hospitalaria : organo oficial de expresion cientifica de la Sociedad Espanola de Farmacia Hospitalariacited by 6

PMID 36520578PUB-36520578

Full text at the publisher

PubMed tag: none · 2017

Semaglutide and Cardiovascular Outcomes in Patients with Type 2 Diabetes.

Marso et al. 2017The New England journal of medicinecited by 78

PMID 28249135DOI 10.1056/nejmc1615712PUB-28249135

Full text at the publisher
Publisher page

Indexing hint: Review · 2009

Novel therapeutics for type 2 diabetes: incretin hormone mimetics (glucagon-like peptide-1 receptor agonists) and dipeptidyl peptidase-4 inhibitors.

Verspohl et al. 2009Pharmacology & therapeuticscited by 118

PMID 19545590DOI 10.1016/j.pharmthera.2009.06.002PUB-19545590

Full text at the publisher
Publisher page

Eligibility

Who could join, as posted.

Sex
All
Age
from 18 Years
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Patients 18 years old or over * To start with the first funded dose of GLP1 receptor agonists ( BMI \> 30Kg/m2) * Treated with another oral antidiabetic Exclusion Criteria: * Diagnosis of diabetic retinopahty and family history of thyroid cancer

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