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Pulmonary Protection of Transcutaneous Electrical Acupoint Stimulation in Gynecologic Laparoscopic Surgery

Pulmonary Protection of Transcutaneous Electrical Acupoint Stimulation in Gynecologic Laparoscopic Surgery

Status
Suspended
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02850471
Enrollment
100
Registered
2016-08-01
Start date
2015-03-31
Completion date
2016-08-31
Last updated
2016-08-01

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

Conditions

Reperfusion Injury

Keywords

Postoperative pulmonary complications, Transcutaneous electric acupoint stimulation, pulmonary protection

Brief summary

TEAS might protect against postoperative pulmonary such as ischemia-reperfusion injury (IRI) and atelectasis. We tested the hypothesis that transcutaneous electrical acupoint stimulation protects against postoperative pulmonary complications in patients who are receiving mechanical ventilation during general anesthesia for gynecologic laparoscopic surgery.

Detailed description

Participants: 100 patients who underwent elective gynecologic laparoscopic surgery Methods: We recruited 100 patients who are planned for gynecologic laparoscopic surgery. Patients were enrolled from March 1, 2015. We randomly allocated patients into two groups: controlled group ( patients treated without transcutaneous electrical acupoint stimulation) and TEAS group (patients treated with TEAS on Feishu, Hegu, Chize half an hour before the surgery). Blood pH, Pco2, Po2 and oxygen saturation were measured by an automatic blood gas analyzer immediately after obtaining the samples from the aorta. Sample all the patients blood before and after the surgery. And then measure the level of TNF-α, IL-1β, and IL-6.

Interventions

DEVICEelectroacupuncture

Transcutaneous Electric Acupoint Stimulation which is a device of electroacupuncture was used on patients in TEAS group with the stimulator parameters set as 2/100Hz, 2V, 30min.

Sponsors

Shengjing Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged from 65 to 75 * The American Society of anesthesiologists (American Society of Anesthesiology, ASA) class Ⅱ \ III * scheduled for gynecologic laparoscopic surgery under general anesthesia

Exclusion criteria

* pre-existing lung or caridac disease * impaired kidney or liver function * history of bronchial asthma or chronic obstructive pulmonary disease * history of smoking * respiratory infection in the previous 2 weeks * preoperative use of bronchodilator, or a steroid

Design outcomes

Primary

MeasureTime frame
the change of blood PO2 in mmHgintraoperative
the change of blood SPO2 in percentageintraoperative
the change of blood pHintraoperative
the change of blood PCO2 in mmHgintraoperative
the change of hemodynamic parameter MAP in mmHgintraoperative
the change of hemodynamic parameters HR in beat per minutesintraoperative

Secondary

MeasureTime frame
post-operative pulmonary complicationsin the first 5 days after surgery
the change of plasma concentration of IL-1βintraoperative
the change of Plasma concentration of TNF-α in pg/mLintraoperative

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026