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Comparison · NCT00938717-sae

Linaclotide vs Placebo: serious adverse events

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. Linaclotide vs Placebo: serious adverse events. Trial comparisons, record NCT00938717-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00938717-sae

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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 10.009950.003880.0253wilson
Risk in group 20.01740.008440.0354wilson
Risk difference, group 1 minus group 2-0.00742-0.02650.0103newcombe hybrid score
Risk ratio, group 1 over group 20.5730.1691.94log
Odds ratio, group 1 over group 20.5690.1651.96log
Number needed to treat, for one fewer participant with a serious adverse event on Linaclotide than on Placebo135from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1LinaclotideLinaclotide 290μg, oral administration, once per day.4402EG001
Group 2PlaceboDose-matched placebo, oral administration, once per day.7403EG000

Harm

What it counts
Total, serious adverse events
Time frame
Adverse event data were collected from July of 2009 to September of 2010 (26 weeks of safety data were collected)

Source ClinicalTrials.gov

Trial

Title
Trial of Linaclotide in Patients With Irritable Bowel Syndrome With Constipation (IBS-C)
NCT number
NCT00938717
Phases
PHASE3
Conditions
Irritable Bowel Syndrome With Constipation
Interventions
Linaclotide or Matching Placebo
Lead sponsor
Ironwood Pharmaceuticals, Inc.
Results first posted
2013-01-30

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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