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Evaluation of the efficacy of proton pump inhibitor for postoperative delirium after hepatobiliary and pancreatic surgery

Phase 2
Recruiting
Conditions
Hepatectomy or pancreatectomy for diseases of the liver, biliary tract, pancreas, and duodenum
Registration Number
JPRN-jRCTs041220114
Lead Sponsor
Sugiura Teiichi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
82
Inclusion Criteria

1.Patients scheduled for elective hepatectomy or pancreatectomy for liver, biliary, pancreatic, and duodenal diseases
2.Age >= 70 years
3.Eastern Cooperative Oncology Group performance status of 0 or 1
4.Ability to undergo the Confusion Assessment Method-Intensive Care Unit (CAM-ICU)
5.Written informed consent

Exclusion Criteria

1.Patients scheduled for laparoscopic surgery.
2.Patients scheduled for hepatectomy combined with pancreatectomy.
3.Patients with dementia
4.Patients with a history of delirium
5.Patients diagnosed with psychological disorders such as alcoholism
6.Patients with habitual use of benzodiazepine receptor agonitst
7.Patients with habitual use of histamine H2-receptor antagonists within a week before registration
8.Patients with a history of hypersensitivity to proton pump inhibitor
9.Patients with habitual use of opioids or steroids
10.Patients who are determined not applicable for the study by the physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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