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Effects of escitalopram and Citalopram on Depression in Patients with Chronic Kidney Failure under Hemodialysis

Evaluation and comparison of the effects and complications of escitalopram and citalopram on depression in patients with chronic renal failure undergoing hemodialysis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200304046698N1
Enrollment
50
Registered
2020-04-09
Start date
2018-09-23
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Major depressive disorder, chronic renal failure. Persistent mood [affective] disorders

Interventions

Intervention 1: The intervention group: In this group escitalopram is prescribed .escitalopram dose increased from 5 mg to 10 mg per day. The drugs were selected from Tehran Pharmaceutical Company an

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients with major depressive disorder with minimum depression score of 13 with Hamilton Test and psychiatrist approval Patients with renal failure who have been undergoing hemodialysis treatment for at least 3 months

Exclusion criteria

Exclusion criteria: Systemic medical disease (heart disease, diabetes, epilepsy, hypertension, thyroid) that interferes with medication use or follow-up. Liver failure, Hepatitis B and C, HIV / AIDS Existence of psychiatric disorder other than depression Patient being treated with SSRIs (if previously treated after 3 months treatment) Pregnancy or lactation Addiction to all kinds of drugs and psychotropics The occurrence of any unbearable side effects in the patient

Design outcomes

Primary

MeasureTime frame
Depression score on the Hamilton scale. Timepoint: Assessment of Hamilton depression score at baseline and 6 weeks after intervention. Method of measurement: Hamilton Depression Inventory.

Secondary

MeasureTime frame
Drug side effect. Timepoint: At baseline (before intervention) and 6 weeks after drug administration. Method of measurement: Questionnaire designed by the researcher.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmina ayatollahi

Yazd University of Medical Sciences

mina_6432@yahoo.com+98 35 3824 0667

Outcome results

None listed

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