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Comparison · NCT01531959-7d79e978

Midodrine vs Placebo: Rates of ICU Readmission

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. Midodrine vs Placebo: Rates of ICU Readmission. Trial comparisons, record NCT01531959-7d79e978. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01531959-7d79e978

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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 10.01520.002680.081wilson
Risk in group 20.04550.01560.125wilson
Risk difference, group 1 minus group 2-0.0303-0.1110.042newcombe hybrid score
Risk ratio, group 1 over group 20.3330.03563.12log
Odds ratio, group 1 over group 20.3230.03273.19log
Number needed to treat, for one fewer participant with the outcome on Midodrine than on Placebo33from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1MidodrineMidodrine: Patients will be randomized to blinded to 20 mg of midodrine166OG000
Group 2PlaceboPlacebo: Patients will be randomized to blinded placebo control366OG001

Outcome

Type
SECONDARY
Title
Rates of ICU Readmission
Description
Number of patients initiated on midodrine that are readmitted back to ICU after being discharged to floor
Time frame
Up to 2 months after ICU discharge
Population

Source ClinicalTrials.gov

Trial

Title
Midodrine for the Treatment of Refractory Hypotension
NCT number
NCT01531959
Phases
PHASE3
Conditions
Hypotension, Critical Illness
Interventions
Midodrine, Placebo
Lead sponsor
Massachusetts General Hospital
Results first posted
2019-09-06

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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