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Comparison · NCT03117569-856da07a

Standard Monitoring Schedule vs Simplified Monitoring Schedule: Undetectable HCV RNA (mITT Population)

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: Undetectable HCV RNA (mITT Population). Trial comparisons, record NCT03117569-856da07a. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03117569-856da07a

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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 10.9840.9430.996wilson
Risk in group 20.9670.9360.983wilson
Risk difference, group 1 minus group 20.0169-0.02730.05newcombe hybrid score
Risk ratio, group 1 over group 21.020.9851.05log
Odds ratio, group 1 over group 22.080.4349.93log
Number needed to treat, for one more participant with the outcome on Standard Monitoring Schedule than on Simplified Monitoring Schedule59from 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).~Participants receive glecaprevir (300mg)/pibrentasvir (120mg): glecaprevir (300mg)/pibrentasvir (120mg) for 8 weeks
121123OG000
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.~Participants receive glecaprevir (300mg)/pibrentasvir (120mg): glecaprevir (300mg)/pibrentasvir (120mg) for 8 weeks
233241OG001

Outcome

Type
SECONDARY
Title
Undetectable HCV RNA (mITT Population)
Description
Number of participants with undetectable HCV RNA based on mITT population.
Time frame
12 weeks post end of treatment (SVR12)
Population
The mITT population wexcludes patients who have completed treatment (\>95% adherence) (according to phone contact at week 8), but have not returned for their SVR12 assessment.

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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