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Study on the effect of intradermal needle at Auricular point on preventing and treating gastrointestinal dysfunction after gastric cancer surgery based on the "brain-gut-bacteria" axis

Study on the effect of intradermal needle at Auricular point on preventing and treating gastrointestinal dysfunction after gastric cancer surgery based on the "brain-gut-bacteria" axis

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068237
Enrollment
Unknown
Registered
2023-02-10
Start date
2023-02-15
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

gastric cancer

Interventions

control group:Perioperative nursing care of patients with gastric cancer undergoing accelerated rehabilitation
experimental group:Perioperative nursing care of patients with gastric cancer undergoing accelerated rehabilitation + ear point press acupuncture

Sponsors

Affiliated Hospital of Nanjing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years old; 2. Patients who meet the diagnostic criteria for gastric cancer and have undergone laparoscopic radical gastrectomy at a scheduled time, without distant organ metastasis and without preoperative radiotherapy and chemotherapy; 3. Patients who have no severe center of gravity, liver, kidney, lung and other organ dysfunction, and can tolerate general anesthesia after the evaluation of doctors; 4. Patients who are clear in mind, have no barrier to language communication and understanding, and voluntarily participate in the test and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Poor nutritional status (total protein < 70 g/L, albumin < 40 g/L), with moderate or above anemia before operation; 2. Patients with endocrine and metabolic diseases such as diabetes; 3. Patients with infectious diseases; 4. Patients who participate in other similar research or receive similar project education; 5. Patients whose condition changes during the perioperative period and who cancel the operation.

Design outcomes

Primary

MeasureTime frame
Recovery time of bowel sounds after operation;First exhaust time, first defecation time;Incidence of postoperative nausea and vomiting;Abdominal distension score of anesthesia wakefulness and 72 hours after operation;Species and abundance of intestinal flora;

Countries

China

Contacts

Public ContactZhang Yuanyuan

Affiliated Hospital of Nanjing University of Chinese Medicine

540314441@qq.com+86 139 1298 4947

Outcome results

None listed

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