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Trial · NCT01954927

Results by group20

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Successful Pain Interventions by Arm Between Presentation and 3 Hours Post Administration of Study DrugGabapentinNo13Participants
Number of Participants With Successful Pain Interventions by Arm Between Presentation and 3 Hours Post Administration of Study DrugPlaceboNo17Participants
Number of Participants With Successful Pain Interventions by Arm Between Presentation and 3 Hours Post Administration of Study DrugGabapentinYes27Participants
Number of Participants With Successful Pain Interventions by Arm Between Presentation and 3 Hours Post Administration of Study DrugPlaceboYes25Participants
Morphine Equivalent Doses Administered From Presentation to 3-hours Post Treatment With Gabapentin/PlaceboGabapentin0.12Inter-Quartile Range 0.09 to 0.22mg/kg
Morphine Equivalent Doses Administered From Presentation to 3-hours Post Treatment With Gabapentin/PlaceboPlacebo0.13Inter-Quartile Range 0.09 to 0.22mg/kg
Number of Participants With Successful Pain Interventions by Arm Between Presentation and Point of Decision for Either Hospital Admission or Discharge to HomeGabapentinNo10Participants
Number of Participants With Successful Pain Interventions by Arm Between Presentation and Point of Decision for Either Hospital Admission or Discharge to HomePlaceboNo17Participants
Number of Participants With Successful Pain Interventions by Arm Between Presentation and Point of Decision for Either Hospital Admission or Discharge to HomeGabapentinYes30Participants
Number of Participants With Successful Pain Interventions by Arm Between Presentation and Point of Decision for Either Hospital Admission or Discharge to HomePlaceboYes27Participants
Morphine Equivalent Doses Administered From Presentation to the Point of Decision for Either Admission or Discharge to HomeGabapentin0.13Inter-Quartile Range 0.10 to 0.25mg/kg
Morphine Equivalent Doses Administered From Presentation to the Point of Decision for Either Admission or Discharge to HomePlacebo0.13Inter-Quartile Range 0.09 to 0.25mg/kg
Hospital AdmissionGabapentinNo32Participants
Hospital AdmissionPlaceboNo32Participants
Hospital AdmissionGabapentinYes10Participants
Hospital AdmissionPlaceboYes12Participants
Absolute Change in Pain From Study Drug to 3 Hours Post Administration of Study DrugGabapentin0Inter-Quartile Range 0 to 2score on a scale
Absolute Change in Pain From Study Drug to 3 Hours Post Administration of Study DrugPlacebo0.5Inter-Quartile Range 0 to 2score on a scale
Absolute Change in Pain, Study Drug to Hospital Discharge DecisionGabapentin1.0Inter-Quartile Range 0.0 to 3.0score on a scale
Absolute Change in Pain, Study Drug to Hospital Discharge DecisionPlacebo0.5Inter-Quartile Range 0.0 to 2.0score on a scale

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
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
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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