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Recruiting NCT07365345

NCT07365345 Frequency of Electrical Acupoint Stimulation on Hypotension in TAVR Patients

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Clinical Trial Summary
NCT ID NCT07365345
Status Recruiting
Phase
Sponsor Air Force Military Medical University, China
Condition Transcatheter Aortic Valve Replacement (TAVR)
Study Type INTERVENTIONAL
Enrollment 150 participants
Start Date 2026-01-30
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age 60 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
electrical acupoint stimulation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 150 participants in total. It began in 2026-01-30 with a primary completion date of 2026-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Within 30 minutes before anesthesia, acupoint electrical stimulation at different frequencies were applied at Neiguan, Jian Shi, and Baihui. The changes in blood pressure during the anesthesia induction period were compared between the high-frequency group and the low-frequency group.

Eligibility Criteria

Inclusion Criteria: * The age of the patients is 60 years or older; * Patients who are scheduled to undergo TAVR surgery under general anesthesia; Exclusion Criteria: * Body mass index less than 18 kg/m2 or greater than 30 kg/m2; * Hemodynamic instability (severe arrhythmia, decompensated heart failure); * Hypotension after admission requiring intervention with vasoactive drugs; * Severe liver or kidney dysfunction; * Those who are contraindicated for electrical stimulation, including those with local skin damage, infection, or having implanted electrophysiological devices in the body.

Contact & Investigator

Central Contact

Zhihong Lu

✉ deerlu23@163.com

📞 86-13891975018

Frequently Asked Questions

Who can join the NCT07365345 clinical trial?

This trial is open to participants of all sexes, aged 60 Years or older, studying Transcatheter Aortic Valve Replacement (TAVR). Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07365345 currently recruiting?

Yes, NCT07365345 is actively recruiting participants. Contact the research team at deerlu23@163.com for enrollment information.

Where is the NCT07365345 trial being conducted?

This trial is being conducted at Xi'an, China.

Who is sponsoring the NCT07365345 clinical trial?

NCT07365345 is sponsored by Air Force Military Medical University, China. The trial plans to enroll 150 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology