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A randomized controlled study applying artificial intelligence (AI) real-time quantitative analysis to assess anastomotic blood supply after low anterior rectal resection to reduce prophylactic stoma rates

A randomized controlled study applying artificial intelligence (AI) real-time quantitative analysis to assess anastomotic blood supply after low anterior rectal resection to reduce prophylactic stoma rates

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072778
Enrollment
Unknown
Registered
2023-06-25
Start date
2023-06-25
Completion date
Unknown
Last updated
2023-06-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer

Interventions

ICG-AI Group:Quantification of intestinal blood supply by ICG combined with AI

Sponsors

The Eighth Hospital of Sun Yat-sen University (Futian, Shenzhen)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1Patients signed informed consent 2Patients with colorectal tumor undergoing laparoscopic left hemicolectomy or low anterior resection. 3?The anastomosis is 3-15cm from the anal verge 3?Patient age 18-80 years old (including 18 and 80 years old) 4, Preoperative CT or MRI, ultrasound endoscopy were used to determine that the lesion did not invade the surrounding tissues (T4b) 6, not receiving radiation therapy before enrollment 7, normal renal function or chronic kidney disease stage I 8, liver function Child A grade 9, no preoperative coagulation disorders 10, willing and able to comply with the study protocol and visitation plan

Exclusion criteria

Exclusion criteria: 1Patients signed informed consent 2Patients with colorectal tumor undergoing laparoscopic left hemicolectomy or low anterior resection. 3?The anastomosis is 3-15cm from the anal verge 3?Patient age 18-80 years old (including 18 and 80 years old) 4, Preoperative CT or MRI, ultrasound endoscopy were used to determine that the lesion did not invade the surrounding tissues (T4b) 6, not receiving radiation therapy before enrollment 7, normal renal function or chronic kidney disease stage I 8, liver function Child A grade 9, no preoperative coagulation disorders 10, willing and able to comply with the study protocol and visitation plan

Design outcomes

Primary

MeasureTime frame
Preventive stoma rate;

Secondary

MeasureTime frame
Incidence of anastomotic fistula;

Countries

China

Contacts

Public ContactXiaoBin Wu

The Eighth Hospital of Sun Yat-sen University (Futian, Shenzhen)

xiaobinwoo@hotmail.com+86 139 2880 0055

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026