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Based on SPARC to explore the curative effect of transcutaneous electrical acupoint stimulation on gastrointestinal functional rehabilitation of patients with colorectal cancer after laparoscopy

Based on SPARC to explore the curative effect of transcutaneous electrical acupoint stimulation on gastrointestinal functional rehabilitation of patients with colorectal cancer after laparoscopy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000415
Enrollment
Unknown
Registered
2025-02-26
Start date
2025-02-26
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

colorectal cancer

Interventions

TEAS Group:TEA+routine rehabilitation

Sponsors

Shanghai Seventh People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 89 Years

Inclusion criteria

Inclusion criteria: 1) Patients who met the diagnostic criteria for gastrointestinal dysfunction after colorectal cancer surgery and underwent laparoscopic resection in the gastrointestinal surgery department of our hospital; 2) Colorectal cancer patients diagnosed by TNM stage as type I-III; 3) Age 40-89 (including 40 and 89); 4) The expected survival period is more than 3 months; 5) The patient has clear consciousness and the ability to evaluate his/her level of gastrointestinal dysfunction, anxiety, sleep quality, etc 6) Patients or family members are willing to accept treatment, and actively cooperate, and sign informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients with cognitive dysfunction, unable to understand or cooperate with assessments such as scale scores; 2) Pregnant or lactating women; 3) Complicated with severe gastrointestinal functional system diseases before operation; Severe heart, lung, liver, kidney, brain or systemic immune diseases; 4) Patients who reported allergic or intolerant to acupuncture. 5) People with severe allergies to silicone, 3M double-sided medical tape, or PC materials. 6) Patients with local acupoint skin injury. 7) Patients who are also or are participating in other clinical studies.

Design outcomes

Primary

MeasureTime frame
First flatus time;

Secondary

MeasureTime frame
IL-6;SAS;First defication time;VAS;SDS;First time out of bed;Intestinal rate post-surgery;GSRS;First eating time;First sign of borborygms;CRP;PCT;TCM symptom score;

Countries

China

Contacts

Public ContactJin Zhu

Shanghai Seventh People's Hospital

13818940541@163.com13818940541

Outcome results

None listed

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