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A clinical study to assess the effects of antidepressant drugs on orexin in patients with major depressive disorder

Correlation of antidepressant therapy with orexinergic pathway integrating targeted metabolomics in patients with major depressive disorder: A longitudinal study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/05/066840
Enrollment
120
Registered
2024-05-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Health Condition 1: F329- Major depressive disorder, singleepisode, unspecified

Interventions

Intervention1: Escitalopram: 10 mg OD for 6-12 weeks Control Intervention1: NIL: NIL

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adult males or females aged 18 to 65 with the diagnosis of Major Depressive Disorder (MDD) 2. Patients who are drug naive or have started on antidepressant therapy for less than 2 weeks

Exclusion criteria

Exclusion criteria: Patients with any known neurological or any systemic disorders known to cause major depressive disorder Patients with any other psychiatric illness and substance use disorders Pregnant and lactating women Patients not willing to give informed consent

Design outcomes

Primary

MeasureTime frame
Mean serum orexin Timepoint: At baseline and 6-12 weeks

Secondary

MeasureTime frame
Orexin and BDNF gene variants Mean Montgomery Asberg Depression rating score Mean PSQI sleep score Mean MoCA score Mean serum orexin Mean serum BDNF Metabolomic profile mean metabolite levelsTimepoint: Week 1

Countries

India

Contacts

Public ContactDr KH Reeta

All India Institute of Medical Sciences, New Delhi

vav.viswanathan@gmail.com

Outcome results

None listed

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