Long-term effects of Semaglutide in participants from the SELECT trial
SELECT-LIFE (SELECT Follow-up Study to Evaluate Long-term Impact oF Anti-obEsity Medication)
This study looks at the long-term effects of Semaglutide on people who took part in a previous trial to see how it impacts their health over the next ten years.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 3400 (estimated) |
| Ages | 45 Years and up |
| Sex | All |
| Sponsor | Novo Nordisk A/S Industry-sponsored |
| Locations | 38 sites (Plainsboro, New Jersey and 37 other locations) |
| Trial ID | NCT04972721 on ClinicalTrials.gov |
What this trial studies
The SELECT-LIFE study is an observational study that aims to assess the long-term effects of Semaglutide in individuals who participated in the SELECT cardiovascular outcomes trial. Following the conclusion of the SELECT trial, participants will complete health questionnaires every six months for up to ten years to monitor their health outcomes. While no specific treatment will be provided during this study, participants will continue to receive standard care from their own healthcare providers. The study focuses on gathering data to better understand the lasting impacts of the medication on participants' health.
Who should consider this trial
Good fit: Ideal candidates are individuals who were randomized into the SELECT trial and have not withdrawn their consent.
Not a fit: Patients with mental incapacity, unwillingness, or language barriers that prevent adequate understanding or cooperation will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide valuable insights into the long-term health effects of Semaglutide for individuals with overweight and obesity.
How similar studies have performed: While this study builds on the findings of the SELECT trial, the long-term observational approach is relatively novel in this context.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Randomized into the SELECT clinical trial (EX9536-4388) and has not withdrawn consent, regardless of level of participation, dose achieved or treatment discontinuation. * Signed SELECT-LIFE consent obtained before any study-related activities (study-related activities are any procedure related to recording of data according to the protocol). Exclusion criteria: * Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation
Where this trial is running
Plainsboro, New Jersey and 37 other locations
- Master Centre for USA — Plainsboro, New Jersey, United States (Recruiting)
- Master Centre for Algeria — Algiers, Algeria (Recruiting)
- Master Centre for Argentina — Prov. De Buenos Aires, Argentina (Recruiting)
- Master Centre for Australia — Baulkham Hills, New South Wales, Australia (Recruiting)
- Cárdio Pulmonar da Bahia — Salvador, Bahia, Brazil (Recruiting)
- Hospital do Coração do Brasil — Brasilia, Distrito Federal, Brazil (Recruiting)
- Eurolatino Medical Research Center — Uberlândia, Minas Gerais, Brazil (Recruiting)
- Núcleo de Pesquisa Clínica S/S — Curitiba, Parana, Brazil (Recruiting)
- Hospital São Vicente de Paulo — Passo Fundo, Rio Grande Do Sul, Brazil (Recruiting)
- AngioCor Blumenau — Blumenau, Santa Catarina, Brazil (Recruiting)
- Instituto de Pesquisa Clínica de Campinas — Campinas, Sao Paulo, Brazil (Recruiting)
- CIP Centro Integrado de Pesquisas do Hospital de Base — São José do Rio Preto, Sao Paulo, Brazil (Recruiting)
- CPQuali Pesquisa Clínica Ltda — São Paulo, Sao Paulo, Brazil (Recruiting)
- CPCLIN - Centro de Pesquisas Clínicas — São Paulo, Sao Paulo, Brazil (Recruiting)
- Instituto Dante Pazzanese de Cardiologia — São Paulo, Sao Paulo, Brazil (Recruiting)
- Departamento de Gastroenterologia - HCFMUSP — São Paulo, Sao Paulo, Brazil (Recruiting)
- Instituto do Coração - HCFMUSP — São Paulo, Sao Paulo, Brazil (Recruiting)
- Master Centre for Brazil — Säo Paulo, Sao Paulo, Brazil (Recruiting)
- Instituto Brasil de Pesquisa Clinica — Rio de Janeiro, Brazil (Recruiting)
- Master Centre for Canada — Mississauga, Ontario, Canada (Recruiting)
- Novo Nordisk Croatia Ltd. — Zagreb, Croatia (Recruiting)
- Master Centre for Denmark — Copenhagen S, Denmark (Recruiting)
- Master Centre for Finland — Espoo, Finland (Recruiting)
- Master Centre for Germany PMS — Mainz, Germany (Recruiting)
- Master Centre for Greece — Vouliagment, Greece (Recruiting)
- Master centre for India — Bangalore, India (Recruiting)
- Master Centre for Ireland — Dublin 9, Ireland (Recruiting)
- Master Centre for Italy — Rome, Italy (Recruiting)
- Master Centre for Japan — Tokyo, Japan (Recruiting)
- MAster Centre for Latvia — Marupes, Latvia (Recruiting)
- Master Centre for Malaysia — Selangor Darul Ehsan, Malaysia (Recruiting)
- Master Centre Netherlands — Alphen A/d Rijn, Netherlands (Recruiting)
- Master Centre for Norway — Rud, Norway (Recruiting)
- Master Centre for South Africa — Sandton, Gauteng, South Africa (Recruiting)
- Master Centre for Sweden — Malmö, Sweden (Recruiting)
- Master Centre for Tawain — Taipei, Taiwan (Recruiting)
- Master Centre for Thailand — Bangkok, Thailand (Recruiting)
- Master Centre for United Kingdom — Gatwick, West Sussex, United Kingdom (Recruiting)
Study contacts
- Study coordinator: Novo Nordisk
- Email: clinicaltrials@novonordisk.com
- Phone: (+1) 866-867-7178
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.