New drug may help gut wake up faster after colon surgery
NCT ID NCT07271875
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a newer drug, sugammadex, helps the bowels recover faster after colorectal surgery compared to an older drug combination (neostigmine/atropine). 560 adults having elective colorectal surgery will be randomly assigned to receive one of the two drugs at the end of surgery. The main goal is to see if more patients in the sugammadex group regain normal bowel function within 72 hours.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Sugammadex and Neostigmine + Atropine
- What this could lead to
- If sugammadex works better, it could mean faster bowel recovery, less nausea, and shorter hospital stays after colorectal surgery.
- What could go wrong
- This is a single-center trial that hasn't started yet. Results may not apply to all hospitals, and the benefit over standard care may be small.
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 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 560 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 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 to 100 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: * Age ≥ 18 years * American Society of Anesthesiologists (ASA) physical status classification I-III * Preoperative Mini-Mental State Examination (MMSE) score \> 23 * Patients scheduled for elective colorectal surgery under general anesthesia. Disease diagnoses include colorectal cancer, benign polyps, benign strictures, or diverticular disease. * Provide informed consent Exclusion Criteria: * Presence of psychiatric disorders, cognitive impairment, or language communication barriers that may affect assessment compliance. * Body Mass Index (BMI) ≥ 35 kg/m². * Severe hepatic dysfunction (Child-Pugh Class C) or renal dysfunction (estimated glomerular filtration rate \< 30 ml/min/1.73m² and/or receiving renal replacement therapy). * Pre-existing severe gastrointestinal dysfunction (e.g., intestinal obstruction, active inflammatory bowel disease, severe constipation/diarrhea); receipt of neoadjuvant therapy preoperatively; planned stoma creation surgery; or scheduled for low rectal surgery (e.g., low anterior resection, abdominoperineal resection). * History of neuromuscular disorders (e.g., myasthenia gravis) or malignant hyperthermia. * History of opioid abuse, or chronic non-surgical pain requiring long-term analgesic therapy. * Anticipated difficult airway, or patients planned for postoperative transfer to the intensive care unit (ICU) while intubated. * Contraindications to the use of neostigmine, atropine, sugammadex, or rocuronium (e.g., known drug allergy, epilepsy, unstable angina, asthma, glaucoma, uncontrolled malignant arrhythmias especially atrioventricular block, severe cardiac valve stenosis); or current use of medications that may significantly influence the effects of neuromuscular blocking agents (e.g., antibiotics such as tetracyclines, aminoglycosides, polymyxins, and clindamycin; antiepileptic drugs; lithium; certain antidepressants such as sertraline and amitriptyline). * Pregnant or lactating women. * Current participation in other clinical trials that may interfere with the results of this 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 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.
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Other studies related to the condition(s) this trial covers.
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