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Effects of transcutaneous electrical stimulation on blood pressure and sleep in gynecological patients

Effects of transcutaneous electrical stimulation on blood pressure and sleep in gynecological patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050676
Enrollment
Unknown
Registered
2021-09-01
Start date
2021-09-06
Completion date
Unknown
Last updated
2022-05-02

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

Conditions

blood pressure

Interventions

Experimental group:Percutaneous electrical stimulation was performed during perioperative period
control group:none

Sponsors

Shengjing Hospital of China Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Gynecological tumor patients admitted for elective surgery.

Exclusion criteria

Exclusion criteria: 1. Skin damage, rash or local infection at the electrical stimulation site, or metal implants near the electrical stimulation; 2. Implantation of cardiac pacemaker, cardiopulmonary pacemaker or defibrillator; 3. Electronic insulin pump implantation and other various electronic implantation equipment; 4. Left upper extremity trauma or arterial stenosis, left upper extremity manometric pressure measurement is not suitable for patients after left breast cancer surgery; 5. Pregnant or lactating women; 6. BMI >= 30kg/m2; 7. Patients with central nervous system and mental diseases; 8. Patients who have been treated with electrical stimulation within 1 week before admission.

Design outcomes

Primary

MeasureTime frame
blood pressure;

Countries

China

Contacts

Public ContactChen Liang

Shengjing Hospital of China Medical University

chenl_sj@126.com+86 18940258435

Outcome results

None listed

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