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Table 1 Inclusion and exclusion criteria for the Oral Ketamine Trial on Suicidality (OKTOS)

From: Predicting therapeutic response to oral ketamine for chronic suicidal ideation: a Bayesian network for clinical decision support

Inclusion criteria

Exclusion criteria

Persons aged ≥18 years

Psychiatric conditions:

Psychosis

Mania/hypomania

Acute suicidal ideation requiring urgent psychiatric intervention

Participants with chronic suicidal thoughts as the primary presenting complaint, determined by Beck Scale for Suicide Ideation – 21 items (BSS) score ≥ 6 at screening

Physical conditions:

Uncontrolled/severe symptomatic cardiovascular disease states including recent myocardial infarction (within prior 6 months); history of stroke; and hypertension (resting blood pressure > 150/100)

History of intracranial mass, intracranial haemorrhage/stroke, cerebral trauma/traumatic brain injury or increased intracranial pressure (as assessed by referring general practitioner)

liver function test results out of normal range, as specified:

  ▪alanine aminotransferase: >  135 U/L

  ▪aspartate aminotransferase: >  123 U/ L

  ▪gamma glutamyl transferase male participants: >  210 U/L

  ▪gamma glutamyl transferase female participants: >  135 U/L

  ▪total bilirubin > 60 umol/L

  ▪albumin: <  25 g/L and > 150 g/L

  ▪alkaline phosphatase: >  345 U/L

Previous reaction to ketamine (as reported by referring general practitioner and participant)

Pregnant women

Breastfeeding women