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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT04469855
Other study ID # NN9535-4347
Secondary ID U1111-1187-9072
Status Enrolling by invitation
Phase
First received
Last updated
Start date July 27, 2020
Est. completion date July 31, 2025

Study information

Verified date November 2023
Source Novo Nordisk A/S
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to assess the safety of long-term treatment with Ozempic® in patients with type 2 diabetes mellitus. People will get Ozempic® as prescribed by their doctor. People will be in this study about 3 years. People above the age of 18 will be asked to fill in the quality of life (QOL) questionnaire (the QOL questionnaire is for the assessment of the influence of diabetes treatment on people's life). There is a possibility that people's blood sample would be provided to Novo Nordisk from their doctors in case of severe allergic reaction that might be caused by Ozempic®.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 3000
Est. completion date July 31, 2025
Est. primary completion date July 31, 2025
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Signed consent obtained before any study-related activities (study-related activities are any procedure related to recording of data according to the protocol). - The decision to initiate treatment with commercially available OzempicĀ® has been made by the patient/Legally Acceptable Representative (LAR) and the treating physician before and independently from the decision to include the patient in this study. - Patients with Diabetes Mellitus, Type 2 (T2DM) who the physician has decided to start treatment with OzempicĀ®. - Male or female, no age limitation. Exclusion Criteria: - Previous participation in this study. Participation is defined as having given informed consent in this study. - Mental incapacity, unwillingness or language barriers precluding adequate understanding or cooperation. - Patients who fall under contraindications to the label. - Patients who are or have previously been treated with OzempicĀ®. - Female who is pregnant, breast-feeding or intends to become pregnant.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
semaglutide
Patients will be treated with commercially available Ozempic® according to routine clinical practice at the discretion of the treating physician. The treating physician's decision to initiate treatment with Ozempic® is independent of the decision to include the patient in the study.

Locations

Country Name City State
Japan Novo Nordisk Investigational Site Aichi
Japan Novo Nordisk Investigational Site Aichi
Japan Novo Nordisk Investigational Site Aichi
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Japan Novo Nordisk Investigational Site Aichi
Japan Novo Nordisk Investigational Site Akita
Japan Novo Nordisk Investigational Site Akita
Japan Novo Nordisk Investigational Site Akita
Japan Novo Nordisk Investigational Site Aomori
Japan Novo Nordisk Investigational Site Aomori
Japan Novo Nordisk Investigational Site Arakawa-ku, Tokyo
Japan Novo Nordisk Investigational Site Asahikawa-shi, Hokkaido
Japan Novo Nordisk Investigational Site Chiba
Japan Novo Nordisk Investigational Site Chiba
Japan Novo Nordisk Investigational Site Chiba
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Japan Novo Nordisk Investigational Site Chiba
Japan Novo Nordisk Investigational Site Chiba-shi, Chiba
Japan Novo Nordisk Investigational Site Chichibu-city
Japan Novo Nordisk Investigational Site Chitose, Hokkaido
Japan Novo Nordisk Investigational Site Ehime
Japan Novo Nordisk Investigational Site Ehime
Japan Novo Nordisk Investigational Site Ehime
Japan Novo Nordisk Investigational Site Ehime
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Japan Novo Nordisk Investigational Site Ehime
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Japan Novo Nordisk Investigational Site Ehime
Japan Novo Nordisk Investigational Site Ehime
Japan Novo Nordisk Investigational Site Ehime
Japan Novo Nordisk Investigational Site Ehime
Japan Novo Nordisk Investigational Site Fukui
Japan Novo Nordisk Investigational Site Fukui-shi, Fukui
Japan Novo Nordisk Investigational Site Fukuoka
Japan Novo Nordisk Investigational Site Fukuoka
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Japan Novo Nordisk Investigational Site Fukuoka-shi, Fukuoka
Japan Novo Nordisk Investigational Site Fukushima
Japan Novo Nordisk Investigational Site Fukushima
Japan Novo Nordisk Investigational Site Fukushima
Japan Novo Nordisk Investigational Site Fukushima-shi, Fukushima
Japan Novo Nordisk Investigational Site Gifu
Japan Novo Nordisk Investigational Site Gifu
Japan Novo Nordisk Investigational Site Gifu
Japan Novo Nordisk Investigational Site Gifu
Japan Novo Nordisk Investigational Site Gifu
Japan Novo Nordisk Investigational Site Gifu
Japan Novo Nordisk Investigational Site Gifu-shi, Gifu
Japan Novo Nordisk Investigational Site Gumma
Japan Novo Nordisk Investigational Site Gumma
Japan Novo Nordisk Investigational Site Gumma
Japan Novo Nordisk Investigational Site Gumma
Japan Novo Nordisk Investigational Site Gunma
Japan Novo Nordisk Investigational Site Gunma
Japan Novo Nordisk Investigational Site Gunma
Japan Novo Nordisk Investigational Site Higashiosaka-shi, Osaka
Japan Novo Nordisk Investigational Site Hiroshima
Japan Novo Nordisk Investigational Site Hiroshima
Japan Novo Nordisk Investigational Site Hiroshima
Japan Novo Nordisk Investigational Site Hiroshima
Japan Novo Nordisk Investigational Site Hiroshima
Japan Novo Nordisk Investigational Site Hiroshima
Japan Novo Nordisk Investigational Site Hokkaido
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Japan Novo Nordisk Investigational Site Hokkaido
Japan Novo Nordisk Investigational Site Hosu-gun, Ishikawa
Japan Novo Nordisk Investigational Site Hyogo
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Japan Novo Nordisk Investigational Site Hyogogoken
Japan Novo Nordisk Investigational Site Ibaraki
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Japan Novo Nordisk Investigational Site Ibaraki
Japan Novo Nordisk Investigational Site Ibaraki
Japan Novo Nordisk Investigational Site Ibaraki
Japan Novo Nordisk Investigational Site Imizu-shi Toyama, Japan
Japan Novo Nordisk Investigational Site Iruma-shi, Saitama
Japan Novo Nordisk Investigational Site Ishikawa
Japan Novo Nordisk Investigational Site Ishikawa
Japan Novo Nordisk Investigational Site Iwate
Japan Novo Nordisk Investigational Site Iwate
Japan Novo Nordisk Investigational Site Iwate
Japan Novo Nordisk Investigational Site Iwate
Japan Novo Nordisk Investigational Site Izumisano-shi Osaka, Japan
Japan Novo Nordisk Investigational Site Kagawa
Japan Novo Nordisk Investigational Site Kagawa
Japan Novo Nordisk Investigational Site Kagawa
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Japan Novo Nordisk Investigational Site Kagoshima
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Japan Novo Nordisk Investigational Site Kagoshima
Japan Novo Nordisk Investigational Site Kagoshima
Japan Novo Nordisk Investigational Site Kagoshima
Japan Novo Nordisk Investigational Site Kagoshima-shi, Kagoshima
Japan Novo Nordisk Investigational Site Kamakura-shi Kanagawa, Japan
Japan Novo Nordisk Investigational Site Kanagawa
Japan Novo Nordisk Investigational Site Kanagawa
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Japan Novo Nordisk Investigational Site Kanagawa
Japan Novo Nordisk Investigational Site Kawagoe-shi Saitama, Japan
Japan Novo Nordisk Investigational Site Kawasaki-shi Kanagawa, Japan
Japan Novo Nordisk Investigational Site Kisarazu-shi, Chiba
Japan Novo Nordisk Investigational Site Kobe, Hyogo
Japan Novo Nordisk Investigational Site Kochi
Japan Novo Nordisk Investigational Site Koriyama-shi Fukushima, Japan
Japan Novo Nordisk Investigational Site Koshigaya-shi,Saitama
Japan Novo Nordisk Investigational Site Kumamoto
Japan Novo Nordisk Investigational Site Kumamoto
Japan Novo Nordisk Investigational Site Kumamoto-shi Kumamoto, Japan
Japan Novo Nordisk Investigational Site Kyoto
Japan Novo Nordisk Investigational Site Kyoto
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Japan Novo Nordisk Investigational Site Mie
Japan Novo Nordisk Investigational Site Mie
Japan Novo Nordisk Investigational Site Mie
Japan Novo Nordisk Investigational Site Mie
Japan Novo Nordisk Investigational Site Minato-ku Tokyo, Japan
Japan Novo Nordisk Investigational Site Mitaka-shi, Tokyo
Japan Novo Nordisk Investigational Site Miura-shi, Kanagawa
Japan Novo Nordisk Investigational Site Miyagi
Japan Novo Nordisk Investigational Site Miyagi
Japan Novo Nordisk Investigational Site Miyagi
Japan Novo Nordisk Investigational Site Miyagi
Japan Novo Nordisk Investigational Site Miyazaki
Japan Novo Nordisk Investigational Site Miyazaki
Japan Novo Nordisk Investigational Site Miyazaki
Japan Novo Nordisk Investigational Site Miyazaki
Japan Novo Nordisk Investigational Site Miyazaki-shi Miyazaki, Japan
Japan Novo Nordisk Investigational Site Muroran-shi, Hokkaido
Japan Novo Nordisk Investigational Site Nagano
Japan Novo Nordisk Investigational Site Nagano
Japan Novo Nordisk Investigational Site Nagano
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Japan Novo Nordisk Investigational Site Nagasaki
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Japan Novo Nordisk Investigational Site Nara
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Japan Novo Nordisk Investigational Site Niigata
Japan Novo Nordisk Investigational Site Niigata
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Japan Novo Nordisk Investigational Site Niigata
Japan Novo Nordisk Investigational Site Niigata-shi, Niigata
Japan Novo Nordisk Investigational Site Nishinomiya-shi, Hyogo
Japan Novo Nordisk Investigational Site Oita
Japan Novo Nordisk Investigational Site Oita
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Japan Novo Nordisk Investigational Site Oita-shi Oita, Japan
Japan Novo Nordisk Investigational Site Okayama
Japan Novo Nordisk Investigational Site Okayama
Japan Novo Nordisk Investigational Site Okayama
Japan Novo Nordisk Investigational Site Okayama
Japan Novo Nordisk Investigational Site Okayama
Japan Novo Nordisk Investigational Site Okayama-shi, Okayama
Japan Novo Nordisk Investigational Site Okinawa
Japan Novo Nordisk Investigational Site Okinawa
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Japan Novo Nordisk Investigational Site Osaka
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Japan Novo Nordisk Investigational Site Osaka-shi, Osaka
Japan Novo Nordisk Investigational Site Osaka-shi, Osaka
Japan Novo Nordisk Investigational Site Osaka-shi, Osaka
Japan Novo Nordisk Investigational Site Osaki-shi, Miyagi
Japan Novo Nordisk Investigational Site Ota-ku, Tokyo
Japan Novo Nordisk Investigational Site Ota-ku, Tokyo
Japan Novo Nordisk Investigational Site Saga
Japan Novo Nordisk Investigational Site Saga
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Japan Novo Nordisk Investigational Site Saitama
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Japan Novo Nordisk Investigational Site Sendai-shi, Miyagi
Japan Novo Nordisk Investigational Site Shiga
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Japan Novo Nordisk Investigational Site Shimane
Japan Novo Nordisk Investigational Site Shimane
Japan Novo Nordisk Investigational Site Shimane
Japan Novo Nordisk Investigational Site Shimotsuga-gun, Tochigi
Japan Novo Nordisk Investigational Site Shimotsuke-shi, Tochigi
Japan Novo Nordisk Investigational Site Shinjuku-ku, Tokyo
Japan Novo Nordisk Investigational Site Shinjyuku-ku Tokyo
Japan Novo Nordisk Investigational Site Shizuoka
Japan Novo Nordisk Investigational Site Shizuoka
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Japan Novo Nordisk Investigational Site Shizuoka
Japan Novo Nordisk Investigational Site Shizuoka-city, Shizuoka
Japan Novo Nordisk Investigational Site Soka-shi, Saitama
Japan Novo Nordisk Investigational Site Suzaka-shi ,Nagano
Japan Novo Nordisk Investigational Site Tamana-shi, Kumamoto
Japan Novo Nordisk Investigational Site Tochigi
Japan Novo Nordisk Investigational Site Tochigi
Japan Novo Nordisk Investigational Site Tochigi
Japan Novo Nordisk Investigational Site Tokorozawa-shi,Saitama
Japan Novo Nordisk Investigational Site Tokushima
Japan Novo Nordisk Investigational Site Tokushima
Japan Novo Nordisk Investigational Site Tokushima
Japan Novo Nordisk Investigational Site Tokyo
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Japan Novo Nordisk Investigational Site Tokyo
Japan Novo Nordisk Investigational Site Tokyo
Japan Novo Nordisk Investigational Site Tomigusuku-shi, Okinawa
Japan Novo Nordisk Investigational Site Tottori
Japan Novo Nordisk Investigational Site Tottori
Japan Novo Nordisk Investigational Site Toyama
Japan Novo Nordisk Investigational Site Toyama-shi, Toyama
Japan Novo Nordisk Investigational Site Toyonaka-shi, Osaka
Japan Novo Nordisk Investigational Site Wakayama
Japan Novo Nordisk Investigational Site Yamagata
Japan Novo Nordisk Investigational Site Yamagata
Japan Novo Nordisk Investigational Site Yamaguchi
Japan Novo Nordisk Investigational Site Yamaguchi
Japan Novo Nordisk Investigational Site Yamaguchi
Japan Novo Nordisk Investigational Site Yamanashi
Japan Novo Nordisk Investigational Site Yamato-shi Kanagawa
Japan Novo Nordisk Investigational Site Yanagawa-shi, Fukuoka
Japan Novo Nordisk Investigational Site Yokohama, Kanagawa

Sponsors (1)

Lead Sponsor Collaborator
Novo Nordisk A/S

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of adverse events (AEs) Count From baseline (day 0) to end of study (month 36)
Secondary Number of serious adverse reactions (SARs) Count From baseline (day 0) to end of study (month 36)
Secondary Number of adverse reactions (ARs) Count From baseline (day 0) to end of study (month 36)
Secondary Number of serious adverse events (SAEs) Count From baseline (day 0) to end of study (month 36)
Secondary Change in glycosylated haemoglobin A1c (HbA1c) Percent From baseline (day 0) to end of study (month 36)
Secondary Change in fasting plasma glucose (FPG) mg/dL From baseline (day 0) to end of study (month 36)
Secondary Change in body weight kg From baseline (day 0) to end of study (month 36)
Secondary Change in patient-reported outcomes (PROs) using the Diabetes Therapy-Related QOL (DTR-QOL) questionnaire - total score DTR-QOL assesses the influence of diabetes treatment on the individual health related quality of life on 4 domains: "burden on social activities and daily activities", "anxiety and dissatisfaction with treatment", "hypoglycaemia" and "satisfaction with treatment". DTR-QOL contains 29 items. The response scale used is a 7-point Likert scale (1:
Strongly agree - 7: Strongly disagree)
From baseline (day 0) to visit 5 (month 12)
Secondary Change in patient-reported outcomes (PROs) using the Diabetes Therapy-Related QOL (DTR-QOL) questionnaire - burden of social activities and daily activities DTR-QOL assesses the influence of diabetes treatment on the individual health related quality of life on 4 domains: "burden on social activities and daily activities", "anxiety and dissatisfaction with treatment", "hypoglycaemia" and "satisfaction with treatment". DTR-QOL contains 29 items. The response scale used is a 7-point Likert scale (1:
Strongly agree - 7: Strongly disagree)
From baseline (day 0) to visit 5 (month 12)
Secondary Change in patient-reported outcomes (PROs) using the Diabetes Therapy-Related QOL (DTR-QOL) questionnaire - anxiety and dissatisfaction with treatment DTR-QOL assesses the influence of diabetes treatment on the individual health related quality of life on 4 domains: "burden on social activities and daily activities", "anxiety and dissatisfaction with treatment", "hypoglycaemia" and "satisfaction with treatment". DTR-QOL contains 29 items. The response scale used is a 7-point Likert scale (1:
Strongly agree - 7: Strongly disagree)
From baseline (day 0) to visit 5 (month 12)
Secondary Change in patient-reported outcomes (PROs) using the Diabetes Therapy-Related QOL (DTR-QOL) questionnaire - hypoglycaemia DTR-QOL assesses the influence of diabetes treatment on the individual health related quality of life on 4 domains: "burden on social activities and daily activities", "anxiety and dissatisfaction with treatment", "hypoglycaemia" and "satisfaction with treatment". DTR-QOL contains 29 items. The response scale used is a 7-point Likert scale (1:
Strongly agree - 7: Strongly disagree)
From baseline (day 0) to visit 5 (month 12)
Secondary Change in patient-reported outcomes (PROs) using the Diabetes Therapy-Related QOL (DTR-QOL) questionnaire - satisfaction with treatment DTR-QOL assesses the influence of diabetes treatment on the individual health related quality of life on 4 domains: "burden on social activities and daily activities", "anxiety and dissatisfaction with treatment", "hypoglycaemia" and "satisfaction with treatment". DTR-QOL contains 29 items. The response scale used is a 7-point Likert scale (1:
Strongly agree - 7: Strongly disagree)
From baseline (day 0) to visit 5 (month 12)
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