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Study of Blood tests in patients of Depression

Comparative assessment and correlation of Peripheral Blood-derived Biochemical and Inflammatory indices in patients with Depressive disorder versus Bipolar disorder, current episode depressive. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2026/04/108924
Enrollment
80
Registered
2026-04-21
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: F313- Bipolar disorder, current episodedepressed, mild or moderate severity Health Condition 2: F321- Major depressive disorder, singleepisode, moderate

Interventions

Intervention1: Nil: Nil

Sponsors

Department of Psychiatry
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients between 18 years to 65 years of age. 2. Patients willing to participate in the study. 3. Patients not on treatment before or if, have been medication-free for a minimum of four weeks prior to assessment. 4. Patients from psychiatric OPD diagnosed with Depressive disorder and Bipolar disorder, current episode depressive by Psychiatrist based on International Classification of Diseases- 11.

Exclusion criteria

Exclusion criteria: 1. Patients not willing to provide written informed consent to participate in the study. 2. Patients with history of any psychiatric co-morbidity. 3. Patients with active suicidal attempts, or ongoing suicidal behaviour at the time of assessment. 4. Patients with substance use disorders except nicotine. 5. Any history Suggestive of acute infection or fever. 6. Pregnant or lactating women. 7. Any other chronic medical illness.

Design outcomes

Primary

MeasureTime frame
1. To measure and compare Complete Blood Count parameters (Neutrophil, Lymphocyte, Monocyte, Platelet counts) and Inflammatory indices like Neutrophil-Lymphocyte ratio (NLR), Platelet-Lymphocyte ratio (PLR) in patients with Depressive disorder and Bipolar depression. Timepoint: At baseline (single time point at the time of recruitment)—

Secondary

MeasureTime frame
1. To compare serum Interleukin-4 (IL-4) levels in patients with Depressive disorder & Bipolar depression. 2. To compare other biochemical parameters such as Bilirubin, Albumin, Uric acid, Lipid profile, Thyroid profile) between the two groups. 3. To correlate biochemical & inflammatory markers with severity of depressive symptoms in both the groups using appropriate clinical rating scales. 4.To determine if any marker serve as potential indicator for differentiating the two groups. Timepoint: At baseline (single time point at the time of recruitment)—

Countries

India

Contacts

Public ContactDr Shrigopal Goyal

Sardar Patel Medical College

shrigopalgoyal@gmail.com8947825749

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026