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Construction and application of evidence-based accelerated rehabilitation of gastrointestinal function in patients with colorectal cancer after operation

Construction and application of evidence-based accelerated rehabilitation of gastrointestinal function in patients with colorectal cancer after operation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071349
Enrollment
Unknown
Registered
2023-05-12
Start date
2023-04-28
Completion date
Unknown
Last updated
2023-06-12

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

Conditions

Colorectal tumor

Interventions

Control group:Conventional care
Intervention group:Conventional care + Evidence based construction plan

Sponsors

Third People's Hospital of Yunnan Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Patients who received a comprehensive preoperative examination and were diagnosed with colorectal cancer by pathology before surgery were scheduled to undergo laparoscopic or surgical radical resection of colorectal cancer; (2) Patients aged between 18 and 85 years old had no serious heart, brain, lung or renal dysfunction in preoperative examination; (3) The patient's general condition can tolerate surgery; (4) American Society of Anesthesiologists (ASA) classification < ?; (5) Patients without intestinal obstruction or severe malnutrition before surgery; (6) The pathological stages were T1-3 N0-1 M0; (7) Willing to accept this experiment.

Exclusion criteria

Exclusion criteria: (1) Patients with significant postoperative changes, such as ICU intensive treatment, death or systemic metastasis. (2) Patients with pregnancy, mental history or unable to cooperate in the study; (3) Patients with serious bone and joint lesions or fractures in the past who are unable to function normally; (4) Patients with a long history of constipation; (5) Patients undergoing emergency surgery for perforation, bleeding, acute abdomen, etc., or patients with severe dysfunction of liver, kidney and other important organs; (6) Patients who withdrew from the study, patients who were discharged from hospital within 3 days, or patients who did not perform activities for 1 day within 3 days.

Design outcomes

Primary

MeasureTime frame
borborygmus;Primary exhaust;cacation;

Secondary

MeasureTime frame
albumin;

Countries

China

Contacts

Public Contactzhaochunyu

Third People's Hospital of Yunnan Province

zhaochunyu0629@163.com+86 135 7172 8692

Outcome results

None listed

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