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Comparison · NCT05966155-24cdf3d2

Depression - Immediate PGx Testing (Modified Intent to Treat, mITT) vs Depression - Delayed PGx Testing (Modified Intent to Treat, mITT): Number of Participants With 50% Reduction in Patient Health Questionnaire (PHQ-8) Score

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Depression - Immediate PGx Testing (Modified Intent to Treat, mITT) vs Depression - Delayed PGx Testing (Modified Intent to Treat, mITT): Number of Participants With 50% Reduction in Patient Health Questionnaire (PHQ-8) Score. Trial comparisons, record NCT05966155-24cdf3d2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05966155-24cdf3d2

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.2810.2350.332wilson
Risk in group 20.2210.1790.27wilson
Risk difference, group 1 minus group 20.0602-0.006710.126newcombe hybrid score
Risk ratio, group 1 over group 21.270.9721.66log
Odds ratio, group 1 over group 21.380.9641.97log
Number needed to treat, for one more participant with the outcome on Depression - Immediate PGx Testing (Modified Intent to Treat, mITT) than on Depression - Delayed PGx Testing (Modified Intent to Treat, mITT)
16.6from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Depression - Immediate PGx Testing (Modified Intent to Treat, mITT)Immediate genetic testing of CYP2D6 and CYP2C19 and clinical decisions support for antidepressant prescribing to the healthcare provider92327OG000
Group 2Depression - Delayed PGx Testing (Modified Intent to Treat, mITT)Delayed genetic testing of CYP2D6 and CYP2C19 and return of results after the conclusion of the 6-month follow-up period71321OG001

Outcome

Type
SECONDARY
Title
Number of Participants With 50% Reduction in Patient Health Questionnaire (PHQ-8) Score
Description
Time frame
3 months
Population
Modified intent to treat (mITT) population consisting of participants with a CYP2C19 poor, rapid, or ultra-rapid metabolizer phenotype or a CYP2D6 poor or ultra-rapid metabolizer phenotype. All mITT participants with a completed PHQ-8 survey at baseline and 3 months are included. Participants with an incomplete PHQ-8 survey at either baseline or 3 months are excluded.

Source ClinicalTrials.gov

Trial

Title
A Depression and Opioid Pragmatic Trial in Pharmacogenetics (Depression Trial)
NCT number
NCT05966155
Phases
NA
Conditions
Depression
Interventions
Pharmacogenetic testing, Clinical decisions support
Lead sponsor
Duke University
Results first posted
2025-06-29

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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