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Clinical study of percutaneous electrical stimulation to improve perioperative lung function in patients with thoracic traumatic fractures

Clinical study of percutaneous electrical stimulation to improve perioperative lung function in patients with thoracic traumatic fractures

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077050
Enrollment
Unknown
Registered
2023-10-27
Start date
2023-11-01
Completion date
Unknown
Last updated
2023-10-30

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

Conditions

Patients with chest trauma fractures

Interventions

Treatment group:The procedure is performed under TEAS+ conventional anesthesia
Control group:The procedure is done under conventional anesthesia

Sponsors

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Those who meet the above indications for thoracic trauma fracture surgery and receive TEAS compound anesthesia surgery for the first time; (2) The Abbreviated Injury Scale (AIS) score of 2~3 points; (3) American Society of Anesthesiologists (ASA) grade I.~II.; (4) Age 20~70 years old, male or female; (5) The forced expiratory volume/predicted value (FEV1pred%) and maximum ventilation per minute/predicted (MVVpred%) in the first second were greater than 65%. (6) Those who have completed the admissions auxiliary examination and have no immune system disease before; (7) Those who have signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Temporary or permanent pacemaker implanted in the heart due to abnormal cardiac conduction system or other reasons; (2) Diagnosed epilepsy or previous author; (3) Patients who have undergone surgery on meridian threads; (4) Patients with local skin infection through acupoints; (5) Patients with upper or lower limb nerve damage; (6) Patients who have participated in other clinical trials in the past four weeks; (7) Patients who cannot cooperate with the completion of the research plan, including language difficulties, infectious diseases, and other medical history. (8) Excluding patients with brain trauma: (1) coma time greater than 6h after trauma or Glasgow score (GCS score) less than 8 points; (2) Patients with brain trauma are confirmed by CT scan or MRI examination; (3) No language function defects caused by learning difficulties caused by congenital or young diseases;

Design outcomes

Primary

MeasureTime frame
FEV1;

Secondary

MeasureTime frame
MVV;Visual analogue pain score, Prince-Henry postoperative pain score;Peripheral blood brightness - enkephalin, dynorphin content;Blood phosphorus, blood calcium, alkaline phosphatase content of fracture healing mediator;Amount of analgesic medication;SP-BSP-D;

Countries

China

Contacts

Public ContactGe Wen

Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

ge-wen@sohu.com+86 138 1759 9214

Outcome results

None listed

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