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Clinical Trials in Egypt / NCT07432815
Recruiting Phase 4

Treatment of Psoriasis With Depression and/or Anxiety With Methotrexate vs Combined Methotrexate and Antidepressant

NCT07432815 · tracked via the Priya Life Science Egypt tracker
Phase
Phase 4
Started
2026-02-01
Last updated
2026-05-05

Condition(s) studied

DepressionAnxietyPsoriasis

Investigational drug(s) / intervention(s)

Combination of methotrexate and escitalopram in treatment of psoriasis patients with depression and/or anxietyMethotrexate →

Combination of methotrexate and escitalopram in treatment of psoriasis patients with depression and/or anxiety: Combination of methotrexate and escitalopram in treatment of psoriasis patients with depression and/or anxiety

Methotrexate: Methotrexate 0.4mg/kg once weekly for 6 months

Study summary

This randomized controlled trial aims to compare the efficacy of methotrexate (MTX) monotherapy versus combined methotrexate and selective serotonin reuptake inhibitor (SSRI) therapy in patients with psoriasis and comorbid depression and/or anxiety. Participants will be randomly assigned to two groups: one receiving MTX alone and the other receiving MTX plus escitalopram. Clinical outcomes will be evaluated over a 6-month period, including psoriasis severity using the Psoriasis Area and Severity Index (PASI) and Body Surface Area (BSA), quality of life using the Dermatology Life Quality Index (DLQI), and psychological status using the Beck Depression Inventory (BDI), Beck Anxiety Inventory (BAI), Hamilton Depression Rating Scale (HAM-D), and Hamilton Anxiety Rating Scale (HAM-A). The study will assess whether combination therapy provides superior clinical and psychological outcomes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: * Adults aged \>18 and \<60 years * Moderate to severe psoriasis (PASI ≥10 or BSA ≥10%) * Moderate to severe depression (BDI ≥20 or HAM-D ≥17) and/or moderate to severe anxiety (BAI ≥16 or HAM-A ≥25) Exclusion Criteria: * Current substance abuse * Systemic psoriasis treatment within the past 3 months * Pregnancy or breastfeeding * Hypersensitivity to methotrexate or escitalopram * Erythrodermic or pustular psoriasis * Contraindications to methotrexate (e.g., hepatic disease or malignancy)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kasralainy Cairo Cairo Governorate Recruiting

More Cairo University trials in Egypt

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07432815 on ClinicalTrials.gov ↗ ← All trials in Egypt