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Safety and efficacy of preanesthetic H2 antagonist therapy for patients on oral rehydration therapy until 2 h before surgery

Safety and efficacy of preanesthetic H2 antagonist therapy for patients on oral rehydration therapy until 2 h before surgery - Safety and efficacy of preanesthetic H2 antagonist therapy for patients on oral rehydration therapy until 2 h before surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000007499
Enrollment
80
Registered
2012-03-14
Start date
2011-11-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

condition required surgery

Interventions

None listed

Sponsors

Hirosaki University school of Medicine & Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients scheduled for elective surgery under general anesthesia

Exclusion criteria

Exclusion criteria: We excluted patients with gastrointestienal obstruction, body mass index (BMI) of 35 kg/m2 or larger, renal dysfunction (a creatinine clearance of 20ml/min or lower or dialysis ), pregnancy, the inability to take food orally, receiving gastroesophageal surgery previously, and long-term H2 antagonist medication.

Design outcomes

Primary

MeasureTime frame
gastric volume and its pH after anesthesia induction

Countries

Japan

Contacts

Public ContactMasatou Kitayama

Hirosaki University school of Medicine & Hospital Department of Anesthesiology

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026