Efficacy of Vonoprazan Versus Intravenous Proton Pump Inhibitors for Prevention of Rebleeding in High Risk Peptic Ulcers Bleeding After Successful Endoscopic Hemostasis

Sponsor
Uayporn Kaosombatwattana (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05005910
Collaborator
(none)
194
1
2
15
12.9

Study Details

Study Description

Brief Summary

Upper gastrointestinal hemorrhage (UGIH) is common urgency condition.The estimate mortality rate about 7 percent from peptic ulcers disease(PUD). A proton pump inhibitors (PPIs) intravenous infusion are standard treatment for high risk ulcer bleeding. Vonoprazan,subclass of potassium-competitive acid blockers (P-CABs), have beneficial effects including rapid, long-lasting and strong acid suppression.The investigators design a randomized-controlled trial comparison between 72 hours of intravenous PPIs infusion and oral vonoprazan in high risk ulcer UGIH after achieve endoscopic hemostasis. Outcome measurement are re-bleeding rate in 30 days as primary and re-bleeding rate in 3 days, 30 days mortality, rate of angioembolisation, unit of blood transfusion, hospital cost and length of stay as secondary outcome.

Condition or Disease Intervention/Treatment Phase
Early Phase 1

Study Design

Study Type:
Interventional
Anticipated Enrollment :
194 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Efficacy of Vonoprazan Versus Intravenous Proton Pump Inhibitors for Prevention of Rebleeding in High Risk Peptic Ulcers Bleeding After Successful Endoscopic Hemostasis
Anticipated Study Start Date :
Sep 1, 2021
Anticipated Primary Completion Date :
Sep 1, 2021
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Vonoprazan

Vonoprazan 20 mg oral every 12 hours (total 72 hours) then vonoprazan 20 mg oral once daily for 28 days

Drug: Vonoprazan
Vonoprazan 20 mg oral every 12 hours (total 72 hours)

Active Comparator: PPIs

PPIs IV infusion for 72 hours then oral PPIs twice per day for 28 days

Drug: PPIs IV infusion
Pantoprazole 80 mg IV loading then 8 mg/hr

Outcome Measures

Primary Outcome Measures

  1. Rebleeding rate [30 days]

Secondary Outcome Measures

  1. Rebleeding rate [3 days]

  2. Mortality rate [30 days]

  3. Number of blood transfusion unit [30 days]

  4. Rate of immobilisation or surgery [30 days]

  5. Length of stay [Until discharge, assessed up to 30 days]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • High risk peptic ulcers bleeding (Forrest class Ia,Ib,IIa,IIb)
Exclusion Criteria:
  • Patients were not achieve endoscopic hemostasis

  • End stage cancer disease

  • Severe critical illness and ICU setting

  • Uncorrectable coagulopathy

  • Pregnancy or breast feeding

  • Allergy to PPIs or Vonoprazan

Contacts and Locations

Locations

Site City State Country Postal Code
1 Faculty of internal medicine siriraj hospital, Mahidol university Bangkok Noi Bangkok Thailand 10700

Sponsors and Collaborators

  • Uayporn Kaosombatwattana

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Uayporn Kaosombatwattana, Lecturer, Mahidol University
ClinicalTrials.gov Identifier:
NCT05005910
Other Study ID Numbers:
  • 011/2563
First Posted:
Aug 16, 2021
Last Update Posted:
Aug 16, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 16, 2021