New acid blocker tested to make anesthesia safer
NCT ID NCT06743243
First seen Jun 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tests whether the drug tegoprazan can raise stomach acid levels before general anesthesia better than famotidine or a placebo. 174 adults having elective surgery will receive one of the three treatments an hour before anesthesia. The main goal is to measure stomach pH right after intubation, aiming to lower the risk of acid aspiration.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Tegoprazan
- What this could lead to
- If it works, tegoprazan could become a standard pre-anesthesia medication to reduce the risk of stomach acid entering the lungs during surgery.
- What could go wrong
- This is a small, early-phase trial focused on a lab measurement (gastric pH), not on actual complications. The drug may not show a meaningful benefit over existing options like famotidine.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 174 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2025
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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20 to 69 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Has a plan to undergo surgery with general anesthesia with inhalation or total Intravenous 2. Subjects aged between 20 and 69 years 3. ASA classification I - III Exclusion Criteria: 1. Conduct Emergency surgery 2. BMI(Body Mass Index) ≥ 35 3. Has a history of drug abuse or depandency. 4. Has a history of Anesthetic allergy 5. Has a plan to undergo resection(gastric cancer, esophageal cancer)
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Korea University Medical Center, Guro Hospital
Seoul, South Korea
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