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Trial · NCT01919801

Results by group37

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

OutcomeGroupCategoryValueSpreadUnits
Time to Meeting Discharge Criteria (TMDC)Icatibant 30 mg4.03Inter-Quartile Range 2.03 to 6.00days
Time to Meeting Discharge Criteria (TMDC)Placebo4.00Inter-Quartile Range 1.03 to 6.00days
Number of Participants With Treatment-emergent Adverse Events (TEAE) and Treatment-emergent Serious Adverse Events (TESAEs)Icatibant 30 mgParticipants with TEAEs27participants
Number of Participants With Treatment-emergent Adverse Events (TEAE) and Treatment-emergent Serious Adverse Events (TESAEs)PlaceboParticipants with TEAEs21participants
Number of Participants With Treatment-emergent Adverse Events (TEAE) and Treatment-emergent Serious Adverse Events (TESAEs)Icatibant 30 mgParticipants with TESAEs2participants
Number of Participants With Treatment-emergent Adverse Events (TEAE) and Treatment-emergent Serious Adverse Events (TESAEs)PlaceboParticipants with TESAEs1participants
Number of Participants With Treatment Emergent Injection Site ReactionIcatibant 30 mgErythema31participants
Number of Participants With Treatment Emergent Injection Site ReactionPlaceboErythema13participants
Number of Participants With Treatment Emergent Injection Site ReactionIcatibant 30 mgSwelling17participants
Number of Participants With Treatment Emergent Injection Site ReactionPlaceboSwelling13participants
Number of Participants With Treatment Emergent Injection Site ReactionIcatibant 30 mgCutaneous pain10participants
Number of Participants With Treatment Emergent Injection Site ReactionPlaceboCutaneous pain7participants
Number of Participants With Treatment Emergent Injection Site ReactionIcatibant 30 mgBurning sensation15participants
Number of Participants With Treatment Emergent Injection Site ReactionPlaceboBurning sensation7participants
Number of Participants With Treatment Emergent Injection Site ReactionIcatibant 30 mgItching13participants
Number of Participants With Treatment Emergent Injection Site ReactionPlaceboItching6participants
Number of Participants With Treatment Emergent Injection Site ReactionIcatibant 30 mgWarm sensation16participants
Number of Participants With Treatment Emergent Injection Site ReactionPlaceboWarm sensation8participants
Number of Participants With Clinically Significant Changes in Laboratory Evaluation, Vital Signs, Electrocardiogram (ECG) and Physical ExaminationIcatibant 30 mg0participants
Number of Participants With Clinically Significant Changes in Laboratory Evaluation, Vital Signs, Electrocardiogram (ECG) and Physical ExaminationPlacebo0participants

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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