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OpenTrials
Completed

NCT Number: NCT02202525

Evolution of Pulse Pressure Following Initiation of Antihypertensive Therapy in Patients With Essential Arterial Hypertension

The main purpose of this prospective, multicentre, french observational study is to analyse the evolution of pulse pressure (PP) and to identify its prognostic factors in hypertensive patients three months after initiation of a new hypertensive therapy. The PP is defined as the difference between systolic blood pressure (SBP) and diastolic blood pressure (DBP).

Completed

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Key information

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with essential arterial hypertension needing a new antihypertensive therapy
  • A patient was included by the physician only if he/she had agreed after being informed about the study

Exclusion criteria

Treatment and study plan

Micardis®

Drug

Other names: Telmisartan

Other hypertensives

Drug

Primary outcomes

  1. Changes from baseline in pulse pressure

    Time frame: Up to 3 months after start of treatment

  2. Number of patients with adverse drug reactions

    Time frame: Up to 3 months after start of treatment

Sponsors and collaborators

Lead sponsor

Boehringer Ingelheim

Industry

Registry information

Official study title

Evolution of Pulse Pressure Following Initiation of Antihypertensive Therapy

Important dates

Study start
2001
Primary completion
2002
First posted
Jul 29, 2014
Registry last updated
Jul 29, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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