Can a new injection cut opioid use after liver surgery?
NCT ID NCT07801183
First seen Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This trial tests whether an experimental painkiller called anrikefon can reduce the need for opioid pain medication in the first two days after laparoscopic liver surgery. Adults scheduled for this procedure will receive either anrikefon or a placebo, in addition to standard pain management. The main goal is to see if anrikefon lowers the total amount of sufentanil, an opioid, used through a patient-controlled pump. The study also tracks recovery milestones like first bowel movement and walking, as well as side effects such as nausea and vomiting.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- anrikefon (Anruikefon), an experimental painkiller given by injection
- What this could lead to
- If it works, anrikefon could offer a way to control pain after liver surgery with less reliance on opioids, potentially reducing side effects like nausea and speeding up recovery.
- What could go wrong
- This is a single-center trial with 117 participants, so results may not apply broadly. The drug is being tested against a placebo, and its effectiveness and safety are not yet established.
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 117 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2027
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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18 years and older
- 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: * Aged ≥ 18 years; * American Society of Anesthesiologists (ASA) physical status classification I-III; * Body mass index (BMI): 18 kg/m² ≤ BMI ≤ 30 kg/m²; * Patients scheduled to undergo laparoscopic hepatectomy under general anesthesia with estimated operation duration ≤ 5 hours; * Agree to participate in this trial and voluntarily sign the informed consent form. Exclusion Criteria: * Patients with a history of severe cardiopulmonary disease, neuropsychiatric disorders, digestive system diseases, chronic dizziness or vestibular dysfunction; * Patients undergoing emergency surgery or trauma patients; * Intraoperative conversion to open laparotomy; * History of abdominal surgery within the past 3 months; * Patients undergoing liver transplantation or with metastasis to other organs; * Patients requiring synchronous resection of organs other than the gallbladder, extrahepatic bile ducts and intestines due to intraoperative clinical needs; * Severe renal dysfunction (estimated glomerular filtration rate \<30 mL/min/1.73 m²); * Laboratory findings or clinical evaluation indicating hypothyroidism or hypokalemia graded ≥ Grade 3 per CTCAE v6.0; * Subjects who experienced nausea, retching or vomiting within 24 hours before anesthesia induction (excluding those caused by bowel preparation); * Patients expected to require postoperative mechanical ventilation via endotracheal intubation or naso/orogastric tube placement for more than 24 hours; * Known allergy or contraindication to opioids and other anesthetics, antiemetics that may be administered during the trial. * Use of drugs with analgesic, antiemetic or anti-inflammatory effects with unknown half-life within 14 days prior to randomization; or the interval between the last administration and randomization is shorter than 5 half-lives or the duration of drug effect (whichever is longer). Such drugs include, but are not limited to, opioid analgesics, non-opioid analgesics, antiemetics (or drugs with antiemetic properties), sedative-hypnotics, sedative anesthetics, glucocorticoids and other drugs with analgesic or antiemetic effects. * Subjects with any other factors deemed by the investigator(s) to render them unsuitable for participation in this clinical study.
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Conditions
The condition(s) this trial relates to.
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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Guangzhou, Guangdong, 510000, China
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