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The effect of auricular point pressing needle stimulation on postoperative intestinal obstruction after colorectal cancer surgery

The effect of auricular point pressing needle stimulation on postoperative intestinal obstruction after colorectal cancer surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001360
Enrollment
Unknown
Registered
2025-07-09
Start date
2025-07-10
Completion date
Unknown
Last updated
2025-07-21

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(NA):conventional treament
experimental group(A):Auricular acupressure needle stimulation

Sponsors

The First Affiliated Hospital of Gannan Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1:Aged18-80 2: 18<BMI<28 3: ASA grade I-III 4: patients undergoing elective laparoscopic resection of colorectal cancer 5: to obtain informed consent 6: no preoperative chemoradiotherapy was performed

Exclusion criteria

Exclusion criteria: 1: Severe heart liver lung and kidney dysfunction 2: patients with immune system diseases or mental illness 3: history of ear surgery 4: need enterostomy 5: patients with skin damage or skin diseases at the stimulation site 6: during the operation it was found that extensive peritoneal metastasis or other tissue and organ metastasis could not be operated 7: Not willing to accept the treatment of thumbtack needle

Design outcomes

Primary

MeasureTime frame
first exhaust time;

Secondary

MeasureTime frame
Number and dosage of postoperative analgesic drug remedies;The incidence of perioperative complications;The occurrence of adverse reactions;Score of the Visual Analogue Scale for Pain;inflammatory factors;Tolerance period for liquid diet;Out of bed independent walking activity time;Postoperative hospital stay days;The heart rate and mean arterial pressure of the patient at each time point after entering the room (T0), at the time of tracheal intubation (T1), at the time of skin incision (T2), 1 hour after the start of the operation (T3), at the end of the operation (T4), at the time of extubation (T5), and when leaving the room (T6);Solid diet tolerance time;The total dosage of sufentanil during the perioperative period;first defecation time;The general information (age gender height weight BMI ASA classification surgical site stage comorbidities preoperative hemoglobin value preoperative albumin value) anesthesia and surgical data of the two groups of patients were recorded;

Countries

China

Contacts

Public ContactZhongMaolin

The First Affiliated Hospital of Gannan Medical University

zml8802@163.com13607978802

Outcome results

None listed

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