Postoperative ileus
Conditions
Interventions
Intervention Group:Intradermal Acupuncture Intervention
Control Group:Routine care
Sponsors
Zhejiang Provincial Hospital of Traditional Chinese Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Patients who have undergone gastrointestinal surgery; 2.Patients diagnosed with postoperative intestinal dysfunction; 3.Patients who voluntarily participate in this study and provide informed consent.
Exclusion criteria
Exclusion criteria: 1.Individuals with communication or cognitive impairments that preclude cooperation. 2.Patients with severe impairment of cardiac, pulmonary, hepatic, or renal function, or those diagnosed with other malignant tumors. 3.Patients who have received intradermal needle therapy for gastrointestinal disorders within the past month. 4.Individuals with bleeding tendencies or dermatological conditions. 5.Individuals with allergic constitutions or those with a known allergy to surgical tape. 6.Patients who are currently participating in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to first flatus;Time to first defecation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Adverse events;TCM Symptom Score;Gastrointestinal Function Score;Quality of Life (QoL);Patient Compliance Score; | — |
Countries
China
Contacts
Public ContactZhu Min
Zhejiang Provincial Hospital of Traditional Chinese Medicine
Outcome results
None listed