A clinical study of robotic surgery combined with perioperative enhanced recovery surgery scheme for rectal cancer patients by transanal specimen collection without auxiliary incision in the abdomen

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100053580

Enrollment

Unknown

Registered

2021-11-24

Start date

2021-12-01

Completion date

Unknown

Last updated

2022-10-17

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

Conditions

Colorectal Cancer

Interventions

experimental group:robotic NOSES combined with perioperative ERAS

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18-75 years; 2. Preoperative colonoscopy or imaging diagnosis of rectal adenocarcinoma; 3. The clinical diagnosis is T1-3NxM0; 4. The maximum diameter of the clinically diagnosed tumor does not exceed 5cm.

Exclusion criteria

Exclusion criteria: 1. Patients with severe underlying diseases who cannot tolerate robotic surgery; 2. Pregnant or lactating patients.

Design outcomes

Primary

Measure	Time frame
Complication rate within 30 days after surgery;	—

Countries

China

Contacts

Public ContactZhu Dexiang

Zhongshan Hospital, Fudan University

shzhudx@163.com+86 13764353275

Outcome results

None listed

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