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Search / Trial NCT00615108

Nice Morning- Safety and Efficacy Observational Study of Telmisartan in Hypertensive Patients in Multicenters

Launched by BOEHRINGER INGELHEIM · Feb 13, 2008

Trial Information

Current as of May 27, 2025

Completed

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • 1. Male or female. 2. Aged 20 to 80 years old. 3. Patients meet one of following two criteria:
  • 1. Adult essential hypertensive either newly diagnosed and untreated, or previously treated and uncontrolled patients; sitting blood pressure: systolic blood pressure (BP) \> 140 mmHg but \< 180 mmHg, and/or diastolic BP \> 90 mmHg but \< 110 mmHg).
  • 2. Patients who are assessed to benefit from the intake of angiotensin II receptor blocker (ARB) monotherapy or as add-on medication.
  • Exclusion Criteria:
  • 1. Patients with contraindications to telmisartan use (as per the Micardis® Tablets package insert).
  • 2. Known hypersensitivity to the active ingredient or to any of the excipients of Micardis® Tablets.
  • 3. Any other clinical condition which, in the opinion of the attending physician, would not allow safe administration of the study medications.

About Boehringer Ingelheim

Boehringer Ingelheim is a global, research-driven pharmaceutical company dedicated to improving health and quality of life through innovative therapies. Established in 1885 and headquartered in Ingelheim, Germany, the company focuses on the development of prescription medicines in key therapeutic areas, including respiratory diseases, cardiovascular health, oncology, and immunology. Boehringer Ingelheim is committed to advancing medical science through rigorous clinical trials and collaborative research, striving to bring novel treatments to patients while upholding the highest standards of safety and efficacy. With a strong emphasis on sustainability and corporate responsibility, the company aims to make a meaningful impact on global health challenges.

Locations

Changhua, , Taiwan

Chiayi, , Taiwan

Chiayi, , Taiwan

Keelung, , Taiwan

Ksohsiung, , Taiwan

Miaoli, , Taiwan

Taichung, , Taiwan

Taichung, , Taiwan

Tainan, , Taiwan

Tainan, , Taiwan

Taipei, , Taiwan

Taipei, , Taiwan

Taipei, , Taiwan

Taipei, , Taiwan

Taipei, , Taiwan

Taipei, , Taiwan

Taipei, , Taiwan

Patients applied

0 patients applied

Trial Officials

Boehringer Ingelheim

Study Chair

Boehringer Ingelheim

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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