Skip to content

Effects of transcutaneous electrical acupoint stimulation on postoperative pain and quality of recovery in patients with lung cancer

Effects of transcutaneous electrical acupoint stimulation on postoperative pain and quality of recovery in patients with lung cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300071136
Enrollment
Unknown
Registered
2023-05-05
Start date
2023-05-08
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

Postoperative chronic pain and quality of recovery

Interventions

Experimental group:Transcutaneous electrical acupoint stimulation
Control group:Routine perioperative management measures

Sponsors

Shengjing Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: The lung cancer root was treated by elective general anesthesia Both sexes aged 18-75 years; ASA?~? Patients agreed to participate and signed an informed consent form.

Exclusion criteria

Exclusion criteria: Emergency surgery; Acupuncture or TEAS was performed within 1 month Contraindications to TEAS (scars or skin lesions at the acupoint site of irritation, pacemaker or other medical electronic devices in the body) Previous chest wall surgery; A history of chronic pain; Hepatic and renal insufficiency; Cardiac insufficiency or severe hypertension (systolic blood pressure =180mmHg, diastolic blood pressure =110mmHg); A history of opioid abuse or alcohol abuse; Patients with a history of epilepsy, mental illness, or communication difficulties

Design outcomes

Primary

MeasureTime frame
The incidence of pain (defined as chronic pain in the surgical incision and chest on the surgical side) was evaluated 6 months after surgery.;

Secondary

MeasureTime frame
VAS score at 24h, 48h, and incidence of pain at 1 month and 3 months after surgery (VAS score if pain was present) were evaluated.;The number of analgesic pump presses and the need for additional analgesics within 48h after surgery;Intraoperative consumption of propofol, sufentanil and remifentanil;The levels of ß-endorphin, white blood cell count, percentage of neutrophil in plasma, serum IL-10,IL-6 and tumor necrosis factor-a (TNF-a) were measured before and 48 hours after TEAS in the first 10% of the sample size.;Blood gas analysis: after intubation and at the end of one-lung ventilation (oxygen partial pressure, blood lactate, blood glucose levels recorded);Spontaneous breathing time and extubation time;The time of first ambulation, the time of chest tube removal and the length of postoperative hospital stay were recorded;The anxiety of patients was evaluated before TEAS and on the 3rd day, 1 month, 3 months, and 6 months after TEAS;The sleep quality of patients was evaluated 1 day before surgery and 3 days, 1 month, 3 months, and 6 months after surgery;To evaluate the incidence of postoperative delirium 3 days after surgery in elderly patients (=65 years old);The incidence of postoperative fever (body temperature =37.3) and atelectasis was evaluated;

Countries

China

Contacts

Public Contactzhao ping

Shengjing Hospital of China Medical University

zhaoping_sj@163.com+86 18940258971

Outcome results

None listed

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