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A clinical study on the intervention of perioperative management of colorectal cancer using the ERAS rehabilitation program in combination with traditional Chinese and Western medicine

A clinical study on the intervention of perioperative management of colorectal cancer using the ERAS rehabilitation program in combination with traditional Chinese and Western medicine

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085191
Enrollment
Unknown
Registered
2024-06-03
Start date
2024-06-10
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

colorectal cancer

Interventions

control group:Health Education
Experimental group:Chinese Western Collaborative ERAS Rehabilitation Program

Sponsors

Shanghai University of Traditional Chinese Medicine Affiliated Shuguang Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Age = 18 years old (2) Pathological diagnosis as CRC (3) American College of Anesthesiologists = Level III and New York College of Cardiology = Level III (4) Accepting CRC surgery (5) No previous history of other abdominal surgeries (6) Voluntarily participate and sign an informed consent form. If the patient loses writing ability, they need to sign an informed consent form together with their guardian to agree to participate in the study

Exclusion criteria

Exclusion criteria: (1) History of abdominal surgery (2) Other surgeries need to be performed simultaneously (3) Postoperative intensive care is required for more than 24 hours (4) Have a history of fainting or epilepsy (5) Have taken painkillers or medications that affect intestinal function within one month (6) With a pacemaker (7) Participated in other clinical studies within the past three months (8) Have received acupuncture and moxibustion, massage and other TCM treatments within one month

Design outcomes

Primary

MeasureTime frame
36-item Short-Form,SF-36;

Secondary

MeasureTime frame
SF-MPQ;Brog Subjective Fatigue Table;cardiopulmonary exercise testing;manual muscle test ;

Countries

China

Contacts

Public ContactJin Li; Jiming Tao

Shanghai University of Traditional Chinese Medicine Affiliated Shuguang Hospital

lijin306@163.com+86 185 1671 7655

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 19, 2026