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NCT Number: NCT07433218

Frequency of Electrical Acupoint Stimulation on Hypotension During Induction

From 15 minutes before to 15 minutes after anesthesia, Transcutaneous Electrical Acupoint Stimulation(TEAS) at different frequencies will be applied at Neiguan and Jian Shi. The changes in blood pressure during the anesthesia induction period will be compared among the high-frequency group ,the low-frequency group and the control group to explore the better frequency to reduce the incidence of post-induction hypotension(PIH) in the elderly.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • aged over 65 yrs old
  • elective abdominal surgery under general anesthesia
  • written infromed consent

Exclusion criteria

  • American society of anesthesiologists status over 3
  • New York Heart Association (NYHA) Functional Classification≥Ⅲ
  • severe arrhythmia leading to hemodynamic instability
  • uncontrolled diabetes
  • hypertension patients stratified as very high risk according to cardiovascular risk classification
  • people who have TEAS contraindications such as local acupoint skin injury or infection and implanted cardiac pacemaker

Treatment and study plan

electrical acupoint stimulation

Other

electrical acupoint stimulation are administered at Neiguan and Jian Shi. The stimulation starts at 15 minutes before anesthesia induction and ends at 15 minutes after anesthesia induction.

electrodes pasted

Other

Electrodes are pasted at Neiguan and Jianshi

high-frequency electrical stimulation

Other

The frequency of electrical stimulation is 100Hz

low-frequency electrical stimulation

Other

The frequency of electrical stimulation is 2Hz

Primary outcomes

  1. incidence of hypotension

    Time frame: from start of anesthesia induction to 15 minutes after induction

    Hypotension is defined as a Mean arterial pressure (MAP) reduction of more than 20% from baseline or a MAP less than 65 mm Hg for at least 30 seconds.

    The baseline MAP is measured during the 5 minutes before start of intervention

Secondary outcomes

  1. The area under the curve representing the change in mean arterial pressure during the induction period relative to the baseline.

    Time frame: from start of induction to 15 minutes after induction

    The area under the curve (AUC) below baseline mean arterial pressure (MAP) is calculated as: ∑ (((Si - Sbaseline)+(Si-1 - Sbaseline))/2 × ΔX) where Sbaseline is the baseline MAP, Si is the MAP at the i-th minute (i = 1…15), and ΔX is the time interval between two measurements.

  2. The dosage of vasoactive drugs

    Time frame: from start of induction to 15 minutes after induction

    Any MAP drop by more than 20% from baseline or a MAP less than 65 mm Hg for at least 1 minute within the first 15 minutes after general anesthesia induction triggered the administration of norepinephrine boluses (5 μg). If hypotension persisted after 2 boluses, a norepinephrine infusion (0.02-0.3 μg/kg/min) was initiated and continued until the MAP became stable and reached 65 mm Hg or higher. If hypotension reoccurred, 2 boluses of norepinephrine were repeated.

  3. lowest MAP

    Time frame: from start of induction to 15 minutes after induction

  4. standard deviation of R-R intervals (SDRR)

    Time frame: from start of induction to 15 minutes after induction

    assessed from the electrocardiography, key index of heart rate variability (HRV)

  5. ratio of low-frequency HRV/high-frequency HRV (LF/HF ratio)

    Time frame: from start of induction to 15 minutes after induction

    assessed from the electrocardiography,High-frequency HRV (HF-HRV) at 0.15-0.4 Hz and low-frequency HRV (LF-HRV) at 0.04-0.15 Hz

  6. major in-hospital complication incidence within 5 postoperative days

    Time frame: from start of anesthesia to the 5 days after anesthesia

    major in-hospital complication incidence within 5 postoperative days

Study contacts

Contact information is provided by the study sponsor or research team.

Zhihong Lu

CONTACT

[email protected]

86-13891975018

Sponsors and collaborators

Lead sponsor

Zhihong LU

Other

Registry information

Official study title

The Influence of Electrical Acupoint Stimulation at Different Frequencies on Hemodynamics During Anesthesia Induction

Acronym: FRESH

Important dates

Study start
2026
Primary completion
2026
Study completion
2027
First posted
Feb 25, 2026
Registry last updated
Sep 15, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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