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Carvedilol for Pre-primary Prophylaxis of Esophageal Varices in Cirrhosis

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Re-verified, no change to tracked fieldsv20
  2. Notable Primary and study completion dates: Dec 1, 2020 to Dec 31, 2026v19
  3. Notable Primary and study completion dates: Dec 1, 2018 to Dec 1, 2020v18
  4. Minor Primary and study completion dates: Dec 2018 to Dec 1, 2018
    • Start date: Sep 2010 to Sep 1, 2010
    v17
  5. Notable Primary and study completion dates: Dec 2017 to Dec 2018v16
Show 14 earlier versionsHide 14 earlier versions
  1. Notable Primary and study completion dates: Dec 2016 to Dec 2017v15
  2. Minor Secondary endpoints revised (3)
    • Site contact updated
    v14
  3. Minor Re-verified, no change to tracked fieldsv13
  4. Notable Primary completion date: Feb 2016 to Dec 2016
    • Study completion date: May 2016 to Dec 2016
    v12
  5. Minor Study title shortened, about 2 wordsv11
  6. Minor 2 versions Re-verified since Aug 21, 2015, no change to tracked fieldsv9-v10
  7. Minor Site contact updatedv8
  8. Notable Primary completion date: Feb 2014 to Feb 2016
    • Study completion date: May 2014 to May 2016
    v7
  9. Minor 2 versions Re-verified since Mar 30, 2013, no change to tracked fieldsv5-v6
  10. Notable Primary completion date: Feb 2012 to Feb 2014
    • Study completion date: May 2012 to May 2014
    • Site contact updated
    v4
  11. Minor 2 versions Re-verified since Apr 11, 2011, no change to tracked fieldsv2-v3
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Patients of cirrhosis aged 18 to 75 years who have no esophageal varices will be enrolled. After baseline evaluation, the participants will be randomized to receive either Placebo or Carvedilol 12.5 mg BD. After randomization they will be followed up for one year.
Trial Details
NCT Number NCT01212250
Lead Sponsor Institute of Liver and Biliary Sciences, India
Conditions
(from sponsor)
Cirrhosis
Related terms Fibrosis
Enrollment 132 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov