CTRI/2024/01/061125Not yet recruitingPhase 2
A Comparative Interventional Study to assess the efficacy of Intravenous Ketamine versus Oral Ketamine for patients with suicidal ideation - NI
Trial Snapshot
- Phase
- Phase 2
- Status
- Not yet recruiting
- Sponsor
- A
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Subjects aged 18 to 65 years with suicidal ideation having HAMD score more than or equal to 14 and Beck
- •suicidal ideation scale of more than or equal to 5
- •2. Subjects willing to take Ketamine after informed written consent.
Exclusion Criteria
- •1. Contraindication to the administration of ketamine, especially present diagnosis or
- •antecedents of clinically relevant cardiovascular disorders such as stroke, heart attack,
- •2. If they had any, those with present or past diagnosis of glaucoma, intracranial
- •hypertension.
- •3. Current diagnosis of schizophrenia or other psychotic disorder (including psychotic
- •disorder due to general medical condition, substance-induced psychotic disorder, or
- •mania) as defined in the ICD-11
- •4. Patients with any known hypersensitivity to ketamine.
- •5. Subjects having any substance dependence, intoxication or withdrawal within 1
- •month period
Investigators
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