Long-term Use of Sonias Combination Tablets in Patients With Type 2 Diabetes Mellitus

NCT ID: NCT02098733

Last Updated: 2016-04-15

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1168 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-06-30

Study Completion Date

2014-05-31

Brief Summary

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The purpose of this study is to evaluate the safety and efficacy of long-term use of Sonias Combination Tablets in patients with type 2 diabetes mellitus in the routine clinical setting.

Detailed Description

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This a special drug use surveillance on long-term use of pioglitazone/glimepiride combination tablets (Sonias Combination Tablets) designed to investigate the frequency of adverse drug reactions in patients with type 2 diabetes mellitus in the routine clinical setting.

The usual adult dosage is one tablet of Sonias administered orally once daily before or after breakfast (15 mg/1 mg or 30 mg/3 mg of pioglitazone/glimepiride).

Conditions

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Type 2 Diabetes

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Pioglitazone/glimepiride

Pioglitazone/glimepiride 15 mg/1 mg or 30 mg/3 mg, orally once daily before or after breakfast

Pioglitazone/glimepiride

Intervention Type DRUG

Pioglitazone/glimepiride combination tablets

Interventions

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Pioglitazone/glimepiride

Pioglitazone/glimepiride combination tablets

Intervention Type DRUG

Other Intervention Names

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Sonias combination tablets

Eligibility Criteria

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Inclusion Criteria

* Patients with type 2 diabetes mellitus for whom a physician has concluded that combination therapy with pioglitazone hydrochloride and glimepiride is appropriate and for whom long-term treatment with Sonias Combination Tablets is considered necessary

Exclusion Criteria

* (1) Patients with cardiac failure or a history of cardiac failure (2) Patients with serious hepatic or renal impairment (3) Patients with severe ketosis, diabetic coma or precoma, or type 1 diabetes mellitus (4) Patients with severe infection, severe trauma, or pre- and post-operative patients (5) Patients with gastrointestinal disorders such as diarrhea and vomiting (6) Pregnant or potentially pregnant women (7) Patients with a history of hypersensitivity to the ingredients in Sonias Combination Tablets or sulfonamides
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Takeda

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Postmarketing Group Manager

Role: STUDY_CHAIR

Takeda

Other Identifiers

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JapicCTI-142438

Identifier Type: REGISTRY

Identifier Source: secondary_id

JapicCTI-R150734

Identifier Type: REGISTRY

Identifier Source: secondary_id

097-011

Identifier Type: -

Identifier Source: org_study_id

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