Study of IV Ketamine for Emergency Department Treatment of Adolescent Suicidal Ideation

Suicidal Ideation Clinical Trial

Official title:

A Double Blinded, Randomized, Placebo Controlled, Parallel Arm Pilot Trial of Intravenous Ketamine for Emergency Department Treatment of Suicidal Ideation in a Pediatric Population

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT05468840
• Other study ID #: 0000001
• Status: Not yet recruiting
• Phase: Phase 3
• Start date: June 2023
• Est. completion date: July 2024

Study information

• Verified date: February 2023
• Source: University of Ottawa
• Contact: Michael Schlegelmilch, MD, MPH
• Phone: 1-613-737-7600
• Email: mschlegelmilch[@]cheo.on.ca
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Approximately 20% of Canadian adolescents experience thoughts of suicide, or suicidal ideation (SI), and suicide is the second leading cause of death among Canadians aged 15-19 years. The emergency department at CHEO sees approximately four patients per day with SI. Even though this is a medical emergency, there are no fast-acting treatments available.

Ketamine is a medication that is commonly used to safely sedate children who require painful procedures in the emergency department. For nearly ten years, intravenous ketamine has also been shown to rapidly reduce SI in adults. However, ketamine as a treatment for SI has never been studied in adolescents. The primary study objective is to pilot a clinical trial that investigates intravenous ketamine to emergently treat SI in adolescents.

If intravenous ketamine can relieve symptoms of SI for youth, this would have tremendous effects on patients and would dramatically change how physicians treat adolescent mental health emergencies. If ketamine is effective for several weeks, as it is in adults, it will help temporize patients until they receive more long-term psychiatric care. At the system level, it has the potential to reduce emergency visits and lengthy admissions. The investigators feel that the results of this study will be generalizable to pediatric centres across Canada and beyond.

Description:

Suicidal ideation (SI) is a common and often severe cause of morbidity in adolescents. Patients frequently present to the emergency department (ED) with severe and distressing thoughts of self-harm or suicide, and yet, there is currently no acute therapeutic intervention to offer them. The standard of care for patients who do not require admission is to discharge them home with resources for websites, apps, or telephone help lines. These interactions fail to address the underlying suicidal thoughts and leave patients, families and providers feeling very dissatisfied. Medications are nearly never initiated in the ED and patients who are already taking anti-depressants experience a very slow therapeutic onset, and often with unfavourable side effects that make medication compliance difficult and sometimes impossible.

For nearly ten years, intravenous ketamine has been shown to be an efficacious acute therapy in adult patients with suicidal ideation. A single dose of intravenous (IV) ketamine can rapidly reduce the severity of suicidal ideation by moderate to large effect sizes (Cohen's d = 0.5-0.8) during an ED visit, in an adult population. However, it has never been studied in a pediatric population. The study primary objective is to determine the feasibility of conducting a trial that investigates the efficacy of IV ketamine to reduce suicidal ideation in adolescents in the pediatric emergency department.

If intravenous ketamine can rapidly alleviate the severity of SI for adolescents, this would have tremendous effects on patients and families and dramatically change how ED physicians treat pediatric mental health emergencies. It would increase patient safety, reduce patient distress, morbidity, possibly mortality and alleviate family stress. If the therapeutic effect of ketamine is maintained for several days, as it is in adults, it will help temporize patient symptoms while they are connected with more long-term psychiatric care. At the system level, it may reduce rates of ED visits and, often lengthy, admissions to hospital. The investigators feel that the results of this study will be generalizable to pediatric centres across Ontario, Canada and beyond.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 20
• Est. completion date: July 2024
• Est. primary completion date: December 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 12 Years to 17 Years

Eligibility

Inclusion Criteria

1. Responds "yes" to ASQ questionnaire at triage, which asks; "Are you having thoughts of killing yourself right now?"

2. Moderate to severe suicidal ideation, defined as score = 3 on the first 5 questions of the Beck Scale for Suicidal Ideation (SSI5)

3. Age 12 to 17 years, inclusive

4. Medically clear, as judged by the treating physician

5. Speaks English or French

Exclusion Criteria

1. Acute intoxication

2. Previously enrolled in the current study or another clinical trial

3. History of intellectual disability or autism spectrum disorder by patient/parent report

4. Active, or history of, psychosis or psychotic disorder

5. History of non-psychiatric neurologic disorder (e.g., epilepsy)

6. Any of the following contraindications to ketamine based on the drug monograph:

1. Known allergy or hypersensitivity to ketamine by patient history

2. History of cerebrovascular accident (stroke or aneurysm)

3. History of elevated intracranial pressure or idiopathic intracranial hypertension

4. Significant hypertension requiring daily medication

5. Severe cardiac decompensation

7. On a Form 1

8. Requires physical or chemical restraint

9. History of violence while in hospital

10. Assessment by a mental health practitioner during the current ED visit prior to study enrollment

11. Pregnant or breastfeeding

Related Conditions & MeSH terms

• Emergencies
• Suicidal Ideation

Intervention

Drug:
• Ketamine Hydrochloride
see study arm description
• Normal saline
see study arm description

Locations

Country	Name	City	State
Canada	CHEO	Ottawa	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
University of Ottawa

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility of the study as measured by the percentage of eligible of patients able to complete the study protocol.	Data analysis for feasibility will be descriptive in nature and there will be no formal hypothesis testing. The percentage of eligible patients who complete the study will be reported.	Baseline
Secondary	Baseline distribution of responses to the first 5 questions of Beck Scale for Suicidal Ideation (SSI5)	Estimates of central tendency (mean) and variance (standard deviation) from participant responses to the SSI5 at baseline will be measured and reported. These parameters will aid with sample size estimates for the larger definitive trial.; The first 5 questions of Beck Scale for Suicidal Ideation (SSI5) is a five item questionnaire scored from 0 to 10, with higher scores indicating more severe suicidal ideation.	Baseline
Secondary	Baseline distribution of responses to the suicide item (#10) from the Montgomery-Asberg Depression Rating Scale (MARDS10)	Estimates of central tendency (mean) and variance (standard deviation) from participant responses to the MADRS10 at baseline will be measured and reported. These parameters will aid with sample size estimates for the larger definitive trial.; The MADRS is a 10 item, 6-point, depression scale. Item 10 rates suicidal ideation from 0 (Enjoys life or takes it as it comes), to 6 (Explicit plans for suicide when there is an opportunity. Active preparations for suicide) with higher scores indicating more severe suicidal ideation.	Baseline
Secondary	Baseline distribution of responses to the suicide item (#9) from the Beck Depression Index (BDI9).	Estimates of central tendency (mean) and variance (standard deviation) from participant responses to the BDI9 at baseline will be measured and reported. These parameters will aid with sample size estimates for the larger definitive trial.; The Beck Depression Inventory is a 21 item depression questionnaire. Item 9 rates suicidal ideation from 0 (I don't have thoughts of killing myself) to 3 (I would kill myself if I had the chance) with higher scores indicating more severe suicidal ideation.	Baseline
Secondary	Baseline pragmatic assessment of the first 5 questions of the Beck Scale for Suicidal Ideation (SSI5), the suicide item (#10) from the Montgomery-Asberg Depression Rating Scale (MADRS10), and the suicide item (#9) from the Beck Depression Index (BDI9).	Pragmatic assessment of the tool validity by asking each participant, which of the three tools best captures how they are feeling at baseline.	Baseline
Secondary	Blinding assessment	Blinding adequacy will be measured by asking each participant which intervention they think they received at the end of the 40 minute study drug infusion.	Baseline
Secondary	Treatment efficacy measured by the Beck Scale for Suicidal Ideation (SSI5)	Suicidal ideation severity at the end of the 40-minute medication infusion will be measured using SSI5.; The first 5 questions of Beck Scale for Suicidal Ideation (SSI5) is a five item questionnaire scored from 0 to 10, with higher scores indicating more severe suicidal ideation.	40 minutes post treatment start
Secondary	Treatment efficacy measured by the suicide item (#10) from the Montgomery-Asberg Depression Rating Scale (MARDS10)	Suicidal ideation severity at the end of the 40-minute medication infusion will be measured using MADRS10.; The MADRS is a 10 item, 6-point, depression scale. Item 10 rates suicidal ideation from 0 (Enjoys life or takes it as it comes), to 6 (Explicit plans for suicide when there is an opportunity. Active preparations for suicide) with higher scores indicating more severe suicidal ideation.	40 minutes post treatment start
Secondary	Treatment efficacy measured by the suicide item (#9) from the Beck Depression Index (BDI9)	Suicidal ideation severity at the end of the 40-minute medication infusion will be measured using BDI9.; The Beck Depression Inventory is a 21 item depression questionnaire. Item 9 rates suicidal ideation from 0 (I don't have thoughts of killing myself) to 3 (I would kill myself if I had the chance) with higher scores indicating more severe suicidal ideation.	40 minutes post treatment start
Secondary	Treatment durability measured by the Beck Scale for Suicidal Ideation (SSI5)	The durability of a treatment effect on suicidal ideation will be measured by SSI5 at 80 minutes, 120 minutes, 24 hours, and seven days post treatment start.; The first 5 questions of Beck Scale for Suicidal Ideation (SSI5) is a five item questionnaire scored from 0 to 10, with higher scores indicating more severe suicidal ideation.	80 minutes, 120 minutes, 24 hours, and seven days post treatment start
Secondary	Treatment durability measured by the suicide item (#10) from the Montgomery-Asberg Depression Rating Scale (MARDS10)	The durability of a treatment effect on suicidal ideation will be measured by MADRS10 at 80 minutes, 120 minutes, 24 hours, and seven days post treatment start.; The MADRS is a 10 item, 6-point, depression scale. Item 10 rates suicidal ideation from 0 (Enjoys life or takes it as it comes), to 6 (Explicit plans for suicide when there is an opportunity. Active preparations for suicide) with higher scores indicating more severe suicidal ideation.	80 minutes, 120 minutes, 24 hours, and seven days post treatment start
Secondary	Treatment efficacy measured by the suicide item (#9) from the Beck Depression Index (BDI9)	The durability of a treatment effect on suicidal ideation will be measured by BDI9 at 80 minutes, 120 minutes, 24 hours, and seven days post treatment start.; The Beck Depression Inventory is a 21 item depression questionnaire. Item 9 rates suicidal ideation from 0 (I don't have thoughts of killing myself) to 3 (I would kill myself if I had the chance) with higher scores indicating more severe suicidal ideation.	80 minutes, 120 minutes, 24 hours, and seven days post treatment start
Secondary	Admission to Hospital	The number and percentage of patients who require hospital admission at the enrolment ED visit will be reported.	18 months
Secondary	Length of Stay in Hospital	The mean and standard deviation of length of hospital stay for patients admitted at the enrolment visit will be reported.	18 months
Secondary	Revisits to the ED	The number and percentage of patients who require a repeat ED visit(s) for mental health complaints within 30 days following enrolment will be reported.	18 months