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Not yet recruitingNCT05624229Updated Sep 28, 2023

Efficacy of Proton Pump Inhibitors in Cirrhotic Patients With Acute Variceal Bleeding

A Phase 4 interventional study of Proton Pump Inhibitors and No Proton Pump Inhibitors in Upper Gastrointestinal Hemorrhage, sponsored by West China Hospital. Not yet recruiting. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2023-09-28.

Sponsored by West China Hospital · Phase 4, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Dec 2025, 9 months ago, but the record still lists the study as not yet recruiting.
Phase
Phase 4
Study type
Interventional
Enrollment
672
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

Acute Variceal Bleeding (AVB) in patients with liver cirrhosis is a common clinical critical disease. There is little evidence for the effect of proton pump inhibitor (PPI) use in patients with AVB, and there is no study on the efficacy of PPI combined with standard therapy in patients with AVB.

Read the detailed description

AVB in patients with liver cirrhosis is a common clinical critical disease, with a 6-week mortality rate as high as 20%. Currently, many guidelines recommend the use of vasoactive drugs (terlipressin, somatostatin or octreotide) combined with endoscopic therapy (Endoscopic Variceal Ligation (EVL), endoscopic injection sclerotherapy (EIS) and the use of prophylactic antibiotics for patients with AVB.

PPI is a commonly used antacid agent, which has a significant antacid effect, protects the gastrointestinal mucosa, promotes blood coagulation, healing ulcers, effectively stops bleeding and prevents rebleeding. There is a consensus that PPI should be used before and after endoscopic therapy in patients with non-variceal acute bleeding. However, studies on the efficacy of PPI after EVL are still limited and lack of sufficient convincing. In a randomized controlled study, pantoprazole treatment was found to be associated with significantly smaller ulcers 10 days after elective EVL in secondary prevention patients with cirrhosis. Another randomized controlled study in 2013 found that patients with cirrhosis and AVB treated with PPI for 19 days after endoscopic hemostasis had smaller ulcers and fewer overall side-effects, but there was no statistically significant difference in rate of 5-day treatment failure, 6-week rebleeding rate and 6-week mortality. In 2017, a study included 637 patients with acute bleeding from liver cirrhosis, 80% of whom were treated with acid suppression therapy, and the study found that acid suppression therapy had no significant effect on long-term bleeding rate and mortality. However, negative effects of PPI have been reported in patients with cirrhosis, such as spontaneous bacterial peritonitis and hepatic encephalopathy. It is found that patients with cirrhosis and ascites had an increased risk of first hepatic encephalopathy with PPI use, and also found that patients with cirrhosis had an increased risk of hepatic encephalopathy and death with PPI use. Therefore, PPI use in patients with cirrhosis should be more cautious. However, the duration of PPI use in these studies was long, and there are no data to clarify the effect of short-term PPI use.

At present, there is no consensus among the major guidelines on the use of PPI in patients with acute AVB in liver cirrhosis, and the UK guidelines do not recommend the use of PPI unless accompanied by gastrointestinal ulcer. The use of PPI was not mentioned in the guidelines of the American Endoscopic Society and the European Endoscopic Society. The 2021 Baveno 7 guideline clearly proposes that PPI should be stopped immediately once AVB is identified as cirrhosis. The latest meta-analysis in 2022 showed that the use of PPI before endoscopy may reduce the need for endoscopic hemostasis in patients with upper gastrointestinal tract, but there was no sufficient evidence to confirm the effect on clinical outcomes including 30-day mortality and rebleeding. It can be concluded that there is no consensus on the use of PPI in patients with AVB in cirrhosis, and the recommendations of guidelines lack high-quality studies to improve the convincing.

In summary, there is little evidence for the effect of PPI use in patients with AVB in liver cirrhosis, and there is no study on the efficacy of PPI combined with endoscopic therapy in patients with AVB in liver cirrhosis. Therefore, the investigators planned to design a multicenter prospective randomized controlled trial to explore the efficacy of PPI in cirrhotic patients with AVB. In this study, the following questions were investigated: 1. Can PPI reduce the 5-day treatment failure rate in cirrhotic patients with AVB; 2. Can it reduce the 6-week rebleeding rate, mortality, and complications in patients with liver cirrhosis and AVB.

02

Conditions studied

  • Upper Gastrointestinal Hemorrhage

Keywords

  • Proton Pump Inhibitors
  • Acute Variceal Bleeding
  • Liver Cirrhosis
  • Endoscopic Variceal Ligation
03

In context

Gastrointestinal Hemorrhage

339 studies on the registry are indexed under Gastrointestinal Hemorrhage; 79 are open to participants now.

This study's planned enrollment of 672 is above the median of 87 across 211 interventional studies indexed under Gastrointestinal Hemorrhage.

Browse Gastrointestinal Hemorrhage studies →

Lead sponsor

West China Hospital is the lead sponsor of 483 studies on the registry; 240 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Liver cirrhosis.
  2. The etiology of portal hypertension is cirrhosis.
  3. Patients presenting with acute esophageal variceal bleeding proven by emergency endoscopy within 24 hours.
  4. Be willing to participate in this clinical study, comply with the study requirements and sign the informed consent

Exclusion criteria

Exclusion Criteria:

  1. non-cirrhotic portal hypertension
  2. the time from admission to endoscopy was more than 24 hours
  3. patients with peptic ulcer or gastroesophageal reflux disease requiring PPI therapy
  4. PPI use for more than 2 weeks before admission
  5. received endoscopic or interventional therapy within the previous 4 weeks
  6. PPI allergy
  7. Chronic renal insufficiency (CKD stage 3-5)
  8. Severe cardiopulmonary dysfunction (such as heart failure grade 3-4, respiratory failure, etc.)
  9. Hepatocellular carcinoma (Barcelona Clinic Liver Cancer (BCLC) stage C and D)
  10. other advanced malignancies (life expectancy less than 6 months)
  11. Pregnancy
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Care provider, Investigator)
Enrollment
672 participants (estimated)

Study arms

  • Placebo comparator
    Standard group

    Early treatment is mainly aimed at correcting hypovolemic shock, preventing gastrointestinal bleeding-related complications, effective control of bleeding, monitoring vital signs and urine output. Medical treatment included initiation and maintenance of vasoactive agents as soon as possible for 2 to 5 days, and prophylactic antibiotics (preferably ceftriaxone sodium or quinolones) by intravenous infusion for 5 days. Endoscopic intervention was performed within 12 hours after presentation and generally no longer than 24 hours. PPI was stopped immediately after endoscopic treatment. Early TIPS is determined according to the technology and concept of each unit.

    Drug: No Proton Pump Inhibitors

  • Experimental
    Standard group+PPI

    PPI continued after endoscopic treatment for 5 days.

    Drug: Proton Pump Inhibitors

Interventions

  • DrugProton Pump Inhibitors

    PPI infusion continued to use for 5 days in experimental group

    Also known as: Drug: Omeprazole, Drug: Esomeprazole, Drug: Rabeprazole, Drug: Pantoprazole, Drug: Ilaprazole, Drug: Lansoprazole

  • DrugNo Proton Pump Inhibitors

    PPI infusion stopped in standard group after endoscopy.

06

What researchers measure

Primary outcomes

  1. 5-day treatment failure rate

    Failure of initial hemostasis Initial hemostasis was defined as not achieving a 24h bleeding-free period within the first 48h after treatment together with stable vital signs based on Baveno consensus criteria. UGI bleeding occurred after initial hemostasis and within 5 days after enrollment was defined as early rebleeding. UGI bleeding was proven to be from esophageal varices.

    Time frame: 5 days

Secondary outcomes

  1. Rebleeding rate within 42 days

    Rebleeding rate within 42 days

    Time frame: 42 days

  2. Mortality rate within 42 days

    Mortality rate within 42 days

    Time frame: 42 days

  3. Rescure treatment

    Number of participants who need of TIPs, re-endoscopy, surgery, etc

    Time frame: 42 days

  4. Compilcations

    Occurrence of chest pain, reflux, nausea, vomiting, dysphagia, ulcer perforation, diarrhea, abdominal pain, headache, hepatic encephalopathy, spontaneous peritonitis, etc

    Time frame: 42 days

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 28, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05624229
Lead sponsor
West China Hospital
Responsible party
luo xuefeng (Professor, West China Hospital) — Principal investigator
First posted
Nov 22, 2022
Start date
Oct 1, 2023 (estimated)
Primary completion
Dec 31, 2025 (estimated)
Completion
Dec 31, 2028 (estimated)
Last update
Sep 28, 2023

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.

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