Eligibility criteria for ambulatory colectomy.
S Bourgouin, T Monchal, G Schlienger...
https://pubmed.ncbi.nlm.nih.gov/33349570Actively Recruiting
Led by University of Arizona · Updated on 2025-09-16
150
Participants Needed
1
Research Sites
52 weeks
Total Duration
Researchers are evaluating outcomes for patients undergoing outpatient colorectal surgery to determine if same-day colectomy can be a safe and effective treatment option for selected patients needing colon and rectal surgery. This prospective cohort study is conducted at a single institution and aims to assess the benefits and risks of outpatient colectomy. Participants will undergo robotic-assisted right colectomy, sigmoidectomy, or low anterior resection. Before surgery, patients and their designated caregivers receive thorough education on medication management, bowel preparation, and perioperative antibiotics. After surgery, patients receive follow-up phone calls or virtual visits on days 1 and 3, and an in-person clinic visit between days 5 and 7. Their medical records will be monitored for six months to track emergency visits, readmissions, and complications. During the study, patients will be closely monitored for various outcomes including hospital readmission within 30 days, surgical site infections, bleeding requiring transfusion, postoperative ileus, reoperations, and other complications. The study includes ongoing assessments through follow-up calls, clinic visits, and medical record reviews to evaluate safety and recovery after same-day colectomy.
CONDITIONS
Same-Day Colectomy: is it Safe for Patients?
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of surgery
Participants undergo same-day colectomy surgery with preoperative education and perioperative care including medication management and bowel preparation.
1 surgical visit (in-person)
Duration - 6 months postoperatively
Participants receive postoperative care including phone or virtual visits on days 1 and 3, and an in-clinic visit between postoperative days 5 and 7. Their medical records are followed for six months to monitor for complications, readmissions, and emergency department visits.
2 remote visits (phone or virtual) and 1 in-person clinic visit
Total: 1 location
1
Banner University Medical Center Phoenix
Phoenix, Arizona, United States, 85006
Actively Recruiting
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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