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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02226822
Other study ID # D1692R00001
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 20, 2014
Est. completion date February 12, 2019

Study information

Verified date February 2020
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is intended to prospectively research the treatment reality and long-term disease control of Type 2 Diabetes Mellitus (T2DM) patients who are initiating 2nd line anti-diabetes treatment in sites across Japan.


Description:

This study is a single country, multicenter, observational, prospective, longitudinal cohort study which will include adult patients with documented history of T2DM who are initiating a second line oral or parenteral anti-diabetes mediation after their first line anti-diabetic therapy in real world setting. The follow-up period is 3 years. Patients will undergo clinical assessments and receive standard medical care as determined by the treating physician. Patients will not receive experimental intervention or experimental treatment as a consequence of their participation in the study.


Recruitment information / eligibility

Status Completed
Enrollment 1869
Est. completion date February 12, 2019
Est. primary completion date February 12, 2019
Accepts healthy volunteers No
Gender All
Age group 20 Years and older
Eligibility Inclusion Criteria:

1. Written consent obtained

2. Aged > = 20 years

3. Diagnosed with type 2 diabetes mellitus

4. Initiating a second oral or parenteral anti-diabetic therapy added to oral anti-diabetic monotherapy or switching from the monotherapy to another monotherapy with different drug class

Exclusion Criteria:

1. Diagnosis of Type 1 Diabetes Mellitus

2. Current pregnancy

3. Current treatment for any cancer

4. Current dialysis treatment or renal transplantation

5. Current treatment with any oral steroids

6. Participation in any randomized control trials

7. Presence of any condition/circumstance which in the opinion of the investigator could significantly limit the complete follow up of the patient (e.g. tourist, non-native speaker who does not understand the local language where interpreter are not available, psychiatric disturbances, alcohol or drug abuse).

Study Design


Locations

Country Name City State
Japan Research Site Amagasaki Hyogo
Japan Research Site Anjo Aichi
Japan Research Site Anzai Aichi
Japan Research Site Asahikawa Hokkaido
Japan Research Site Chiba
Japan Research Site Chigasaki Kanagawa
Japan Research Site Edogawa-ku Tokyo
Japan Research Site Fukui
Japan Research Site Fukuoka
Japan Research Site Fukuyama Hiroshima
Japan Research Site Funabashi Chiba
Japan Research Site Gifu
Japan Research Site Hachioji Tokyo
Japan Research Site Hakodate Hokkaido
Japan Research Site Hamamatsu Shizuoka
Japan Research Site Hiratsuka Kanagawa
Japan Research Site Hirosaki Aomori
Japan Research Site Hiroshima
Japan Research Site Hitachi Ibaraki
Japan Research Site Hitoyoshi Kumamoto
Japan Research Site Iida Nagano
Japan Research Site Ikuno-ku Osaka
Japan Research Site Imari Saga
Japan Research Site Ise Mie
Japan Research Site Isehara Kanagawa
Japan Research Site Isesaki Gunma
Japan Research Site Itoshima Fukuoka
Japan Research Site Iwade Wakayama
Japan Research Site Iwaki Fukushima
Japan Research Site Joetsu Nigata
Japan Research Site Kamakura Kanagawa
Japan Research Site Kamikawa Hokkaido
Japan Research Site Kanazawa Ishikawa
Japan Research Site Kanoya Kagoshima
Japan Research Site Kanra-gun Gunma
Japan Research Site Karatsu Saga
Japan Research Site Kashiwara Osaka
Japan Research Site Kasukabe Saitama
Japan Research Site Kawasaki Kanagawa
Japan Research Site Kisarazu Chiba
Japan Research Site Kita-ku Tokyo
Japan Research Site Kitakatsuragi-gun Nara
Japan Research Site Kitakyushu Fukuoka
Japan Research Site Kobe Hyogo
Japan Research Site Kobe Hyougo
Japan Research Site Kochi
Japan Research Site Koga Ibaraki
Japan Research Site Koganei Tokyo
Japan Research Site Koka Shiga
Japan Research Site Kokubunji Tokyo
Japan Research Site Komatsu Ishikawa
Japan Research Site Komatsu Aichi
Japan Research Site Koufu Yamanashi
Japan Research Site Kouka Shiga
Japan Research Site Kumamoto
Japan Research Site Kurate-gun Fukuoka
Japan Research Site Kyoto
Japan Research Site Maibara Shiga
Japan Research Site Matsuyama Ehime
Japan Research Site Mitaka Tokyo
Japan Research Site Miyazaki
Japan Research Site Mogami Yamagata
Japan Research Site Muroran Hokkaido
Japan Research Site Nagoya Aichi
Japan Research Site Nakagawa Hokkaido
Japan Research Site Nasushiobara Tochigi
Japan Research Site Nerima-ku Tokyo
Japan Research Site Nichinan Miyazaki
Japan Research Site Nishimatuura Saga
Japan Research Site Oguri Fukuoka
Japan Research Site Oita
Japan Research Site Okayama
Japan Research Site Ono Fukui
Japan Research Site Onojo Fukuoka
Japan Research Site Osaka
Japan Research Site Otaru Hokkaido
Japan Research Site Otsu Shiga
Japan Research Site Oyama Tochigi
Japan Research Site Saga
Japan Research Site Sakado Saitama
Japan Research Site Sapporo Hokkaido
Japan Research Site Sendai Miyagi
Japan Research Site Sennan-gun Osaka
Japan Research Site Shibukawa Gunma
Japan Research Site Shimotsuga-gun Tochigi
Japan Research Site Shinagawa-ku Tokyo
Japan Research Site Shinjuku Tokyo
Japan Research Site Shirakawa Fukushima
Japan Research Site Shizuoka
Japan Research Site Takamatsu Kagawa
Japan Research Site Takasaki Gunma
Japan Research Site Tamana Kumamoto
Japan Research Site Tamba Hyougo
Japan Research Site Tateyama Chiba
Japan Research Site Tochigi
Japan Research Site Tokushima
Japan Research Site Tomigusuku Okinawa
Japan Research Site Toyonaka Osaka
Japan Research Site Tsu Mie
Japan Research Site Ube Yamaguchi
Japan Research Site Ueda Nagano
Japan Research Site Urazoe Okinawa
Japan Research Site Ushiku Ibaraki
Japan Research Site Yaizu Shizuoka
Japan Research Site Yamagata
Japan Research Site Yokkaichi Mie
Japan Research Site Yokohama Kanagawa

Sponsors (2)

Lead Sponsor Collaborator
AstraZeneca Ono Pharmaceutical Co. Ltd

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Classes of diabetic medications at baseline and changes up to 3 years Classes of anti-diabetic medications at baseline and any changes of anti-diabetic medications during 3 years follow-up period. At 6, 12, 24, 36 month from enrollment
Secondary Hemoglobin A1c change from baseline, Achievement rate of HbA1c and blood glucose target goals Overall and by second line anti-diabetic medication class, treatment response in terms of changes in HbA1c from baseline, achievement rate of HbA1c and blood glucose target goals At 6, 12, 24, 36 month from enrollment
Secondary Blood glucose level change from baseline Overall and by second line anti-diabetic medication class, treatment response in terms of changes in blood glucose level (FPG or CPG or PPG) from baseline. At 6, 12, 24, 36 month from enrollment
Secondary Body weight change from baseline Overall and by second line anti-diabetic medication class, treatment response in terms of changes in body weight. At 6, 12, 24, 36 month from enrollment
Secondary Blood pressure change from baseline Overall and by second line anti-diabetic medication class, treatment response in terms of changes in blood pressure from baseline. At 6, 12, 24, 36 month from enrollment
Secondary Lipid profile changes from baseline Overall and by second line anti-diabetic medication class, treatment response in terms of changes in lipid profile At 6, 12, 24, 36 month from enrollment
Secondary Incidence of microvascular complications Overall and by second line anti-diabetic medication class, disease progression in terms of microvascular complications: incidence of chronic nephropathy, dialysis, diabetic retinopathy, retinal photocoagulation, amputation of lower extremity, diabetic foot, peripheral nerve disorders, autonomic nervous system disorders and erectile dysfunction. At 6, 12, 24, 36 month from enrollment
Secondary Hypoglycemia events Overall and by second line anti-diabetic medication class, hypoglycemic events and hyperglycermia hospitalizations At 6, 12, 24, 36 month from enrollment
Secondary Patient reported Quality of Life, diet, and physical activity level Overall and by second line anti-diabetic medication class, patient reported Quality of Life, diet, and physical activity level At 6, 12, 24, 36 month from enrollment
Secondary Initiation of insulin therapy, Proportion of patients using insulin Initiation of insulin therapy (e.g., reporting the average number of anti-diabetic therapies prescribed as insulin therapy is initiated and dose of insulin) At 6, 12, 24, 36 month from enrollment
Secondary Switching of anti-diabetic medications or dose change Switching of anti-diabetic medications or dose change At 6, 12, 24, 36 month from enrollment
Secondary Initiation of third line or above add-on anti-diabetic medications Initiation of third line or above add-on anti-diabetic medication (e.g., reporting proportion of patients receiving 2nd, 3rd, 4th or greater anti-diabetic therapies at each follow-up visit) At 6, 12, 24, 36 month from enrollment
Secondary Incidence of macrovascular complications Overall and by second line anti-diabetic medication class, disease progression in terms of macrovascular complications (heart failure, myocardial infarction and stroke). At 6, 12, 24, 36 month from enrollment
Secondary Risk factors Risk factors (patient characteristics at baseline: e.g. age, gender, duration of diabetes, presence of co-morbidities) associated with poorer clinical outcomes during follow-up At 6, 12, 24, 36 month after enrollment
Secondary Treatment choice Determinants of treatment choice At baseline
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