Skip to content

Impact of perioperative transcutaneous electrical acupoint stimulation on the outcomes of patients with thoracoscopic lobectomy

Impact of perioperative transcutaneous electrical acupoint stimulation on the outcomes of patients with thoracoscopic lobectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004952
Enrollment
Unknown
Registered
2014-07-04
Start date
2014-07-13
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

thoracoscopic lobectomy

Interventions

Placebo TEAS group,:received identical electrode placement but with no electrical output from the TEAS unit

Sponsors

Renji Hospital, School of Medicine, Shanghai Jiao Tong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. aged between 18 and 75 yr; 2. scheduled for elective and first thoracoscopic lobectomy; 3. body mass index less than 30 or more than 18; 4. written informed consent was obtained from each participant

Exclusion criteria

Exclusion criteria: 1.the existence of scars or skin infection on or near the selected acupoints; 2.the existence of upper and lower limb nerve injury; 3.the existence of a ventricular pacemaker; 4.history of severe mycocardial, neurologic, muscular, pulmonary, renal, or hepatic disease; 5.alcohol or drug abuse.

Design outcomes

Primary

MeasureTime frame
the incidence of postoperative morbidity;

Secondary

MeasureTime frame
intraoperative and postoperative vasoactive drugs;intraoperative and postoperative arterial-alveolar oxygen tension ratio;intraoperative and postoperative anesthetic and/or analgesic requirement;the score and incidence of postoperative nausea and vomiting;postoperative visual analog scale score;intraoperative hemodynamic stability;

Countries

China

Contacts

Public ContactXiang-rui Wang
xiangrui68@163.com+86 13701901953

Outcome results

None listed

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