Actively Recruiting
Clinical Research on the Treatment Model of Ambulatory Surgery for Colorectal Cancer
Led by First Hospital of China Medical University · Updated on 2024-11-27
352
Participants Needed
1
Research Sites
282 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To investigate the postoperative complication incidence and long-term efficacy between ambulatory surgery for colorectal cancer and traditional laparoscopic colorectal surgery in patients with colorectal tumor who are generally in good health and have sufficient organ functions。
CONDITIONS
Official Title
Clinical Research on the Treatment Model of Ambulatory Surgery for Colorectal Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients voluntarily join and sign informed consent
- Age between 18 and 75 years
- Good general health with ASA classification Grade I to III
- Confirmed adenocarcinoma or high-level intraepithelial neoplasia by colonoscopy biopsy
- Tumor diameter of 5.0 cm or less by enhanced CT or MRI
- Preoperative staging of cT1-3NanyM0
- Able to follow colorectal day surgery plan with micro-laparoscopic radical colorectal cancer treatment
- No contraindications for abdominal wall nerve block anesthesia or non-opiate analgesics
- No need for conventional anticoagulant or antiplatelet therapy
- Have relatives or co-residents able to provide 24-hour care for at least 72 hours post-operation, living within 30-minute drive of hospital, and able to follow postoperative care plan
You will not qualify if you...
- Elderly patients with multiple basic diseases
- Moderate to severe anemia
- Severe hypoproteinemia
- Poorly controlled diabetes
- Contraindications to laparoscopic surgery
- Emergency surgery cases due to acute intestinal obstruction, perforation, or bleeding
- Presence of distant metastases
- Unwillingness to sign informed consent or follow study plan
- History of psychotropic drug abuse or mental disorders affecting compliance
- Living alone or in psychosocial isolation, unable to understand postoperative care
- Residence far from hospital or with insufficient medical resources and difficult transportation
- Any other serious diseases judged by researchers to endanger patient safety or study completion
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
First Hospital of China Medical University
Shenyang, Liaoning, China, 110000
Actively Recruiting
Research Team
K
Kai Li
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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