Skip to content

comparative of the effects of Atenolol, Enalapril and Hydrochlorothiazid

study of the effects of Atenolol, Enalapril and Hydrochlorothiazid on the Hypertension stage II in patients with hypertension

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2012110511371N1
Enrollment
150
Registered
2013-01-31
Start date
2006-03-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Hypertension. Hypertensive heart disease without (congestive) heart failure

Interventions

Intervention 1: The first group were given atenolol 50mg once daily (three weeks). Intervention 2: The second group enalapril 5mg every 12 hours (three weeks). Intervention 3: The third group Hydrochl
Treatment - Drugs
The first group were given atenolol 50mg once daily (three weeks).
The second group enalapril 5mg every 12 hours (three weeks).
The third group Hydrochlorothiazide 50mg once daily (three weeks).

Sponsors

Ardabil University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria: All patients with hypertension stage II referred to Buali Hospital in Ardabil; without medications of hypertension; without renal disease (Cr> 1.5); without electrolyte imbalances; no contraindications for use atenolol (asthma, heart block, bradycardia, hypotension); no contraindications for use hydrochlorothiazide (hyperuricemia, initial Hypraldstrvnysm; no contraindications for use enalapril (allergy, renal failure); wishing to participate in the study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Hypertension. Timepoint: Before the experiment, three weeks after intervention. Method of measurement: Mm Hg, using a mercury manometer.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBehzad Babapour

Ardabil University of Medical Sciences

b.babapoursaatlou@arums.ac.ir+98 45 1551 2007

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026