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Comparison · NCT00006164-sae

Peginterferon Alfa-2a 90 mcg/Week vs Standard of Care Followup: 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. Peginterferon Alfa-2a 90 mcg/Week vs Standard of Care Followup: serious adverse events. Trial comparisons, record NCT00006164-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00006164-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 10.3380.2990.38wilson
Risk in group 20.2910.2540.331wilson
Risk difference, group 1 minus group 20.0477-0.008470.104newcombe hybrid score
Risk ratio, group 1 over group 21.160.9731.39log
Odds ratio, group 1 over group 21.250.9611.62log
Number needed to harm, for one more participant with a serious adverse event on Peginterferon Alfa-2a 90 mcg/Week than on Standard of Care Followup21from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: standard of care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Peginterferon Alfa-2a 90 mcg/WeekTreatment with Peginterferon alfa-2a 90 mcg administered once weekly for an additional 42 months175517EG000
Group 2Standard of Care FollowupStop any peginterferon alfa-2a/ribavirin therapy and followed prospectively for an additional 42 months without treatment155533EG001

Harm

What it counts
Total, serious adverse events
Time frame
Within 1400 days (3.83 years) after randomization

Source ClinicalTrials.gov

Trial

Title
Long Term Interferon for Patients Who Did Not Clear Hepatitis C Virus With Standard Treatment
NCT number
NCT00006164
Phases
PHASE3
Conditions
Chronic Hepatitis c, Cirrhosis, Liver, Fibrosis, Liver, Hepatic Cirrhosis
Interventions
Peginterferon alfa-2a + Ribavirin, Peginterferon alfa-2a
Lead sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Results first posted
2009-09-04

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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