Same-Day colon surgery: a safe new option?
NCT ID NCT07176715
First seen Jun 26, 2026 · Last updated Jul 24, 2026 · Updated 2 times
Summary
This study looks at whether it is safe for some patients to go home the same day after colon surgery. Researchers will track 150 adults aged 18-70 who have robotic-assisted colon removal. The main goal is to see how many need to be readmitted within 30 days, along with other complications like infection or bleeding.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Same-day discharge protocol
- What this could lead to
- If successful, this could show that same-day colectomy is safe for certain patients, reducing hospital stays and healthcare costs.
- What could go wrong
- This is a small, single-center study with only 150 participants, so results may not apply broadly. There is a risk of complications like infection or readmission.
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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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Sep 2025
- Expected to finish
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Sep 2030
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 70 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: * Ages 18-70 * Undergoing robotic-assisted right colectomy, sigmoidectomy, or low anterior resection. * Able to perform greater than 4 metabolic equivalents (METS) without shortness of breath * Must have a designated adult who can care for them at home postoperatively until their in-person clinic visit * Access to a cell phone or computer and running water. * Successfully completed pre-operative and post-operative education * Medical criteria: * Well controlled hypertension with systolic blood pressure \< 140 controlled by less than two medications which they are compliant with * Well controlled diabetes on oral agents only with blood glucose level \< 180 on daily checks * Anti-platelet agents including aspirin, clopidogrel, prasugrel, ticagrelor or ticlopidine will be stopped 7 days preoperatively and restarted on postoperative day 1. See exclusion criteria 7 for specific exclusion criteria regarding antiplatelet agents. Exclusion Criteria: * Medical criteria: * Neurocognitive deficits not allowing for adequate preoperative education * Congestive heart failure with EF \< 45% * Symptomatic aortic stenosis causing heart failure, syncope, dyspnea or angina * Pulmonary fibrosis or pulmonary hypertension * COPD or home oxygen use \> 2L * Chronic kidney disease of any stage. * Lack of a caregiver at home or functionally bed-bound * Ultralow pelvic resection * Need for ostomy creation intraoperatively * Operative time greater than 5 hours as this likely indicates a complex case and dissection necessitating closer monitoring in the hospital * Conversion to open procedure intraoperatively * Patients receiving antiplatelet agents such as clopidogrel, prasugrel, ticagrelor or ticlopidine within one year of coronary or carotid stent implantation, TAVR or LAAO placement. * Patients on therapeutic anticoagulation medications such as warfarin, Eliquis, Xarelto, Enoxaparin * Current tobacco use * Patients who were unable to complete preoperative education, do not feel comfortable with care at home, or do not have an available caregiver for the first 7 postoperative days * Any surgical history that would preclude safe abdominal entry for robotic surgery
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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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Banner University Medical Center Phoenix
RECRUITINGPhoenix, Arizona, 85006, United States
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