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Comparison · NCT03117569-8ea55167

Standard Monitoring Schedule vs Simplified Monitoring Schedule: Severe/Life Threatening Adverse Events (Safety Outcome)

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. Standard Monitoring Schedule vs Simplified Monitoring Schedule: Severe/Life Threatening Adverse Events (Safety Outcome). Trial comparisons, record NCT03117569-8ea55167. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03117569-8ea55167

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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 10.007870.001390.0433wilson
Risk in group 20.007910.002170.0284wilson
Risk difference, group 1 minus group 2-0.0000311-0.02150.0358newcombe hybrid score
Risk ratio, group 1 over group 20.9960.091210.9log
Odds ratio, group 1 over group 20.9960.089511.1log
Number needed to treat, for one fewer participant with the outcome on Standard Monitoring Schedule than on Simplified Monitoring Schedule32,100from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Standard Monitoring Schedule
Participants will have on-treatment clinic visits at weeks 4 and 8. Participants have also phone contact-based visits at weeks 4 and 8 (1-2 days prior to scheduled clinic visits).~glecaprevir (300mg)/pibrentasvir (120mg): glecaprevir (300mg)/pibrentasvir (120mg) for 8 weeks
1127OG000
Group 2Simplified Monitoring Schedule
Participants will have no on-treatment clinic visits at weeks 4 and 8. Participants have phone contact-based visits at weeks 4 and 8.~glecaprevir (300mg)/pibrentasvir (120mg): glecaprevir (300mg)/pibrentasvir (120mg) for 8 weeks
2253OG001

Outcome

Type
OTHER_PRE_SPECIFIED
Title
Severe/Life Threatening Adverse Events (Safety Outcome)
Description
Proportion of patients with at least one severe or potentially life threatening (grade 3 or 4) adverse event.
Time frame
12 weeks post end of treatment (SVR12)
Population
ITT

Source ClinicalTrials.gov

Trial

Title
Trial of Simplified Treatment Monitoring for 8 Weeks Glecaprevir/Pibrentasvir in Chronic Hepatitis C Patients
NCT number
NCT03117569
Phases
PHASE3
Conditions
Hepatitis C, Chronic
Interventions
glecaprevir (300mg)/pibrentasvir (120mg)
Lead sponsor
Kirby Institute
Results first posted
2019-12-11

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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