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The Effect of sertraline in women with resistant hypertension

The study of sertraline in controlling the resistant hypertension in women with co-morbid premenstrual syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT138904092181N4
Enrollment
40
Registered
2010-06-30
Start date
2010-11-22
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

Condition 1: Recurrent depressive disorder, unspecified. Condition 2: hypertension. Monopolar depression NOS High blood pressure

Interventions

Intervention 1: Interventional group: tab sertraline 50 -100 mg daily for 4 -6 weeks. Intervention 2: Control group: placebo with the same shape, size and taste for 4–6 weeks.
Treatment - Drugs
Placebo
Interventional group: tab sertraline 50 -100 mg daily for 4 -6 weeks
Control group: placebo with the same shape, size and taste for 4–6 weeks

Sponsors

Tabriz medical sience university
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Sex age, Age 15 – 49 year old, presence of drug resistant hypertension, With PMS (premenstrual syndrome), With written informed consent form Exclusion criteria: history of allergic reaction or side effect with sertaline, BMD (bipolar mood disorder), MDD (major depressive disorder), anxiety disorders, psychosis, cognitive disorders, or mental retardation, Pregnancy, breast feeding, Acute coronary syndromes, Heart failure

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood pressure. Timepoint: Before / 4-6 weeks after intervention. Method of measurement: Blood pressure mannometer (mmHg).

Secondary

MeasureTime frame
Sertraline side effect. Timepoint: Weekly. Method of measurement: Antidepressant side effects questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Fatemeh Ranjbar Kouchaksaraie

Tabriz University of Medical Sciences

ranjbarf@tbzmed.ac.ir+98 41 1380 4486

Outcome results

None listed

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