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A Study of Orforglipron in Female Participants With Stress Urinary Incontinence Who Have Obesity or Overweight
1000 patients around the world
Available in
United States, Mexico
Eli Lilly and Company
7
Research sites
1000
Patients around the world
This study is for people with
Urinary Incontinence
Requirements for the patient
From 18 Years
Female
Medical requirements
Inclusion criteria
Have a body mass index (BMI) of 27 kilograms per square meter (kg/m2) or higher at screening.
Have a diagnosis of stress urinary incontinence.
Exclusion criteria
Have had urinary incontinence surgery.
Have recently received onabotulinumtoxin A (Botox) bladder injections or currently taking medications for urinary incontinence.
Have given birth within one year of screening.
Have had a change in body weight of more than 11 pounds within 90 days prior to screening.
Have used any anti-obesity medication or alternative weight loss remedies within 180 days prior to screening.
Have type 1 diabetes, type 2 diabetes, or any other type of diabetes.
Have had a cardiovascular health condition within 90 days prior to screening.
Are pregnant, intending to be pregnant, breastfeeding, or intending to breastfeed for the duration of the study.
Sites
Centro de Oncología de Precisión
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Santiago, Región Metropolitana de Santiago, 7560908
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Clinstile S.A de C.V.
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Durango 325, Roma Norte, Ciudad de México
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RM Pharma Specialists S.A. de C.V.
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Amores 734 Col. del Valle, Del. Benito Juárez, Ciudad de México
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Medimanage Research
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Coscomate 71-PISO 2 B, Toriello Guerra, Tlalpan, 14050 Ciudad de México, CDMX, Mexico
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Medical Care & Research SA de CV - México
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Calle 32 217 por Calle 11 y 13, Colonia Garcia Gineres, CP 97070 - Yucatán, Mérida
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Health Pharma Professional Research
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Dakota 351, Nápoles, Benito Juárez, 03840 Ciudad de México, CDMX, Mexico
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Centro de Investigación Clínica Chapultepec S. A. de C. V. - Morelia
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Gral. Manuel de La Pena y Pena 455, Chapultepec Nte., 58260 Morelia, Mich., Mexico
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Study
RESTRAIN-SUI
Sponsor
Eli Lilly and Company
Study type
Interventional
Conditions
Urinary Incontinence
Requirements
From 18 Years
Female
Unique study ID
clinicaltrials.gov
NCT07202884
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