Skip to content

Effects of Transcutaneous Electrical Acupoint Stimulation on Lung Injury during One-Lung Ventilation in Thoracoscopic Surgery

Effects of Transcutaneous Electrical Acupoint Stimulation on Lung Injury during One-Lung Ventilation in Thoracoscopic Surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038243
Enrollment
Unknown
Registered
2020-09-15
Start date
2020-09-14
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Lung cancer

Interventions

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) For patients undergoing thoracoscopic lobectomy under general anesthesia, the expected operation time is >= 2 hours; 2) Aged >= 18 years; 3) BMI index 18-28kg/?; 4) ASA classification I to III; 5) Primary tumor, without radiotherapy or chemotherapy before surgery; 6) Plan to use one-lung ventilation for lung isolation during the operation; 7) Sign the informed consent form voluntarily.

Exclusion criteria

Exclusion criteria: 1) Those with a pacemaker in their body; 2) Infusion of blood products before or during the operation; 3) Abnormal lung function, recent history of lung infection and history of systemic infection; 4) Patients who have undergone surgery at the meridian points, or have skin infections or trauma at meridian points; 5) Those who have a history of radiotherapy and chemotherapy before surgery; 6) Patients who have participated in other clinical trials in the past 4 weeks.

Design outcomes

Primary

MeasureTime frame
Superoxide dismutase;Malondialdehyde;

Countries

China

Contacts

Public ContactSongxu Ju

Hebei General Hospital

1913159173@qq.com+86 15114547277

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026