ConductScience.org, home

Comparison · NCT00006164-8f8f8a99

Peginterferon Alfa-2a 90 mcg/Week vs Standard of Care Followup: Hepatic Encephalopathy

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

Download JSON
Cite this record

ConductScience Library. Peginterferon Alfa-2a 90 mcg/Week vs Standard of Care Followup: Hepatic Encephalopathy. Trial comparisons, record NCT00006164-8f8f8a99. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00006164-8f8f8a99

On this page

Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.0290.01770.0473wilson
Risk in group 20.04130.02740.0617wilson
Risk difference, group 1 minus group 2-0.0123-0.03560.0107newcombe hybrid score
Risk ratio, group 1 over group 20.7030.3691.34log
Odds ratio, group 1 over group 20.6940.3561.35log
Number needed to treat, for one fewer participant with the outcome on Peginterferon Alfa-2a 90 mcg/Week than on Standard of Care Followup81.6from 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 months15517OG000
Group 2Standard of Care FollowupStop any peginterferon alfa-2a/ribavirin therapy and followed prospectively for an additional 42 months without treatment22533OG001

Outcome

Type
PRIMARY
Title
Hepatic Encephalopathy
Description
Any mental status alteration which is deemed by the investigator to be due to portosystemic encephalopathy, whether occurring during a provoked episode (GI bleeding, diuretics, usual sedative doses), or spontaneously (without apparent cause).
Time frame
1400 days (3.85 years) post randomization
Population

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.

For software

Read this comparison from software.

The record is JSON. No key.

GET https://conductscience.org/api/comparisons/v1/NCT00006164-8f8f8a99