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The effect of combined use of cyclosporine and electroacupuncture acupoint stimulation on sleep and circulatory function in elderly patients with urological hypertension

The effect of combined use of cyclosporine and electroacupuncture acupoint stimulation on sleep and circulatory function in elderly patients with urological hypertension

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101636
Enrollment
Unknown
Registered
2025-04-27
Start date
2023-12-18
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

Sleep disorders

Interventions

Cyclophenol group:Induction was performed by intravenous infusion of cyclophenol (0.3-0.5mg/kg), remifentanil (TCI1-3ng/ml), sufentanil (0.2-0.4 µ g/kg), and cisatracurium (0.2mg/kg) after denitrifica
Electroacupuncture acupoint group:Starting 10 minutes before surgery, constant and continuous current transcutaneous electrical stimulation (instrument: Beijing Yaoyang Kangda Medical Instrument - tra
Joint group:Starting 10 minutes before surgery, constant continuous current transcutaneous electrical stimulation (instrument: Beijing Yaoyang Kangda Medical Instrument - transcutaneous nerve electric

Sponsors

The First Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to No maximum

Inclusion criteria

Inclusion criteria: Age >= 55 years old, ASA II-III grade, BMI18-25kg/m^2, Hypertensive patients undergoing urological surgery, including various stones and tumors (excluding functional tumors such as pheochromocytoma and primary aldosteronism), without serious systemic diseases, voluntarily participate in this trial and sign an informed consent form.

Exclusion criteria

Exclusion criteria: Preoperative patients with severe heart, lung, brain, kidney, central nervous system, and psychiatric disorders; Patients with a history of using sedatives, painkillers, or antidepressants; Those who are not suitable for transcutaneous acupoint electrical stimulation; Individuals with severe visual or hearing impairments who are unable to communicate; Individuals allergic to the use of anesthetic drugs; Individuals who have undergone other types of surgeries within the past six months; Those who have poor compliance and are unable to cooperate with treatment; The patient or family members do not agree to conduct this study.

Design outcomes

Primary

MeasureTime frame
Athens Insomnia Scale Score;Pittsburgh Sleep Quality Index Scale;Non invasive cardiac output;Peripheral vascular resistance;

Secondary

MeasureTime frame
Blood pressure and heart rate; Collect relevant data on the preoperative and postoperative sleep monitoring wristbands on day 1 (including all day sleep duration),The duration of sleep, deep sleep time throughout the day, light sleep time throughout the day, wakefulness time, time of falling asleep last night, time of waking up this morning, and based on body movements during sleep. ;

Countries

China

Contacts

Public ContactLian Zeng

The First Affiliated Hospital of Guangxi Medical University

zenglian1973@163.com+86 137 3702 3816

Outcome results

None listed

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