semaglutide
DrugThis is a retrospective, non-interventional study; therefore, no intervention was administered as part of the study.
NCT Number: NCT07627074
The purpose of the study is to assess the weight loss in participants treated with commercially available semaglutide according to routine clinical practice at the discretion of the treating physician.
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Notify Me18 year and older
All sexes
Observational
Novo Nordisk Investigational Site, London, United Kingdom
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
This is a retrospective, non-interventional study; therefore, no intervention was administered as part of the study.
Time frame: From index date (day 0) to week 68 (day 476)
Measured as kilogram (kg)
Time frame: From index date (day 0) to week 68 (day 476)
Measured as percentage (%)
Time frame: From index date (day 0) to week 68 (day 476)
Binary (yes/no): estimated ≥5% reduction from baseline body weight
Novo Nordisk A/S
Industry
Real-world Weight Outcomes in Adults Treated With Semaglutide s.c. 1.0 mg or 1.7 mg for Weight Management: a Non-interventional Cohort Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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