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Comparison · NCT03431285-48ef5ccb

Morphine Group vs Ketamine Group: Drug-related Adverse Effects

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. Morphine Group vs Ketamine Group: Drug-related Adverse Effects. Trial comparisons, record NCT03431285-48ef5ccb. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03431285-48ef5ccb

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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 10.02140.007310.0611wilson
Risk in group 20.0580.02970.11wilson
Risk difference, group 1 minus group 2-0.0365-0.09070.0122newcombe hybrid score
Risk ratio, group 1 over group 20.370.11.36log
Odds ratio, group 1 over group 20.3560.09241.37log
Number needed to treat, for one fewer participant with the outcome on Morphine Group than on Ketamine Group27.4from 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 1Morphine Group
Patients will receive standard dose of morphine (0.1 mg/kg) in 100 ml normal saline (NS) infused over 30 minutes in addition to standard IV hydration.~Morphine Group: Patients will receive standard dose of morphine (0.1 mg/kg) in 100 ml normal saline infused over 30 min in addition to standard IV hydration.~standard IV hydration: IV hydration as per our institutional protocol (Lactated Ringer's or NaCl 0.9% solution will be infused at a rate of 2-3 ml/kg/h)
3140OG000
Group 2Ketamine Group
Patients will receive low dose ketamine 0.3 mg/kg in 100ml normal saline (NS) infused over 30 minutes in addition to standard IV hydration~Ketamine Group: Patients will receive low dose ketamine 0.3 mg/kg in 100ml N.S. infused over 30 min in addition to standard IV hydration~standard IV hydration: IV hydration as per our institutional protocol (Lactated Ringer's or NaCl 0.9% solution will be infused at a rate of 2-3 ml/kg/h)
8138OG001

Outcome

Type
SECONDARY
Title
Drug-related Adverse Effects
Description
flushing, hypotension, altered mental status, itching, paresthesia, respiratory depression, dizziness, nausea, vomiting
Time frame
3 hours following drug administration
Population
intention to treat (ITT)

Source ClinicalTrials.gov

Trial

Title
Ketamine for Acute Painful Crisis in Sickle Cell Disease Patients
NCT number
NCT03431285
Phases
NA
Conditions
Sickle Cell Crisis
Interventions
Morphine Group, Ketamine Group, standard IV hydration
Lead sponsor
Imam Abdulrahman Bin Faisal University
Results first posted
2025-05-28

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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