Skip to content

COugh Among Hypertensive Patients Treated With Telmisartan, Who Had to Stop previoUs ACE-i Treatment Due to couGH in Slovakia

Cough Among Hypertensive Patients Treated With Telmisartan, Who Had to Stop Previous ACE-i Treatment Due to Cough

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01217879
Acronym
COUGH
Enrollment
980
Registered
2010-10-08
Start date
2010-01-31
Completion date
2010-09-30
Last updated
2012-11-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension

Keywords

Cough, Telmisartan, Bradykinin, Tolerability

Brief summary

In the light of ONTARGET and TRANSCEND studies results, it would be interesting to investigate the real-life telmisartan treatment tolerability. It is well known and accepted that the Real-life setting is much more adequate to reflect the antihypertensive and safety properties of the drug in comparison to the organized and scheduled setting of the clinical trial. Because there are not much data on the cough in relation to telmisartan, therefore it would we worth to observe the cough frequency and general treatment tolerance in patients treated with telmisartan, who had to stop their previous ACE-I treatment due to cough.

Interventions

Patients treated with telmisartan tablets under the real-life setting. Dosing regimen customised to the needs of each participating patient according to the investigators assessment

Sponsors

Bayer
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hypertension * Age \> 18 * ACE-I related cough

Exclusion criteria

* Current treatment with telmisartan * Cholestatic disorders and severe hepatic failure * Allergy to telmisartan * Pregnancy and lactation period

Design outcomes

Primary

MeasureTime frame
Cough frequency among telmisartan treated patients, who had to stop their previous ACE-I treatment due to cough4 months after initiation

Secondary

MeasureTime frame
Number of Participants with Adverse Events among patients, who had to stop their previous ACE-I treatment due to cough4 months after initiation

Countries

Slovakia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026