Last updated on September 2020

Post-marketing Surveillance of Linaclotide Tablet in Patients With Irritable Bowel Syndrome With Constipation or Chronic Constipation (Excluding Constipation Due to Organic Diseases)

Brief description of study

The objective of this study is to evaluate the long-term safety and efficacy of linaclotide in post-marketing use.

Detailed Study Description

This is a post-marketing long-term specified drug use-result survey study required for products in Japan. The investigator will register the patient who have been taking this product for the first time within 14 days after the start of treatment (inclusive of the start day). For each of the registered patients (including withdrawals and dropouts), the investigator will enter the survey data on the case report form.

Clinical Study Identifier: NCT03471728

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Site JP00007

Fukushima, Japan
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Site JP00034

Hiroshima, Japan
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Site JP00001

Hokkaido, Japan
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Site JP00017

Ishikawa, Japan
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Site JP00046

Kagoshima, Japan
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Site JP00014

Kanagawa, Japan
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Site JP00043

Kumamoto, Japan
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Site JP00045

Miyazaki, Japan
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Site JP00042

Nagasaki, Japan
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Site JP00022

Shizuoka, Japan
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Site JP00036

Tokushima, Japan
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Site JP00030

Wakayama, Japan
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Site JP00006

Yamagata, Japan
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Site JP00035

Yamaguchi, Japan
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Site JP00019

Yamanashi, Japan
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Recruitment Status: Open

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