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Ketamine vs Propofol: Number of Patients With Postoperative Cognitive Dysfunction

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.640.4450.798wilsonClinicalTrials.gov
Risk in group 20.4170.2450.612wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.223-0.05230.457newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.540.882.68logClinicalTrials.gov
Odds ratio, group 1 over group 22.490.7877.87logClinicalTrials.gov
Number needed to treat, for one more participant with the outcome on Ketamine than on Propofol4.48from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 1KetamineKetamine induction~Ketamine: Ketamine used for induction1625OG000ClinicalTrials.gov
Group 2PropofolPropofol induction~Propofol: Propofol for induction1024OG001ClinicalTrials.gov

Outcome 5

FieldValueSource
TypePRIMARYClinicalTrials.gov
TitleNumber of Patients With Postoperative Cognitive DysfunctionClinicalTrials.gov
Description
Pre and postoperative cognitive studies will be performed to assess change in cognitive function.~Postoperative cognitive dysfunction (POCD) was defined a-priori as a decline of decline of \>1 standard deviation (i.e. z-score decline of \> 1) on at least 2 neurocognitive tests. The neurocognitive tests utilized include Trail making Test A, Trail making Test B, Hopkins Verbal Learning Test-Revised Learning trials, Hopkins Verbal Learning Test-Revised Delayed Recall, Digit Span, Controlled Oral Word Association Test, Stroop color/word test, and the Mini Mental Status Examination.
ClinicalTrials.gov
Time frameBaseline (preoperative cognitive tests) to hospital discharge or 10 days postoperatively whichever came first.ClinicalTrials.gov
PopulationIntent to treat populationClinicalTrials.gov

Trial 8

FieldValueSource
TitleThe Impact of Ketamine on Postoperative Cognitive Dysfunction, Delirium, and Renal DysfunctionClinicalTrials.gov
NCT numberNCT02554253ClinicalTrials.gov
PhasesPHASE2ClinicalTrials.gov
ConditionsCognitive Disorders, Delirium, Acute Kidney InjuryClinicalTrials.gov
InterventionsKetamine, PropofolClinicalTrials.gov
Lead sponsorMayo ClinicClinicalTrials.gov
Results first posted2022-02-15ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT02554253?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.