Pharmacogenetics Associated With IV Ketamine
Prospective observational study (n=85 actual) collecting saliva genetic samples from adults who previously received IV ketamine for treatment-resistant depression to correlate genetic biomarkers with treatment response.
Detailed Description
Participants who previously received intravenous ketamine for treatment-resistant depression provide two saliva swabs for genetic analysis; the study examines associations between genetic markers and clinical response to IV ketamine.
Observational, prospective design leveraging clinic-treated patients at the Canadian Rapid Treatment Centre of Excellence; outcomes are biomarker–response correlations rather than interventional efficacy.
Study Arms & Interventions
Genetic samples
experimentalParticipants who previously received IV ketamine provide saliva for genetic analysis to correlate biomarkers with treatment response.
Interventions
- Compound
Saliva genetic samples: two saliva swabs collected; genetic analysis only.
Participants
Inclusion Criteria
- Inclusion Criteria:
- 1. Must have received IV ketamine previously to treat Treatment-Resistant Depression
- 2. Between the ages of 18-65 years old.
- 3. Clinical diagnosis of MDD
- 4. Individuals may have had comorbid psychiatric conditions (e.g., anxiety), but the comorbid psychiatric condition cannot be the primary clinical concern.
- 5. Ability to provide informed consent
Exclusion Criteria
- Exclusion Criteria:
- 1. Individuals who meet DSM 5 criteria for a substance use and/or alcohol use disorder in the past 3 months.
- 2. Individuals who are currently experiencing psychotic symptoms as part of an MDE (mood congruent/mood incongruent).
- 3. Individuals who are unable to consent to the procedure.
- 4. Individuals who are unable to adhere to the protocol in its totality
Study Details
- StatusCompleted
- PhasePhase NA
- Typeobservational
- DesignNon-randomized
- Target Enrollment85 participants
- TimelineStart: 2021-01-01End: 2021-01-08
- Topic