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Sleep regulation by digital monitoring-based transcutaneous electrical acupoint stimulation combined with Esketamine

Sleep regulation by digital monitoring-based transcutaneous electrical acupoint stimulation combined with Esketamine

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080894
Enrollment
Unknown
Registered
2024-02-17
Start date
2024-02-19
Completion date
Unknown
Last updated
2024-02-19

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

Conditions

surgical patients

Interventions

Control Group :electrodes were placed
no current was given,Saline
TEAS Group :TEAS,Saline
Esketamine Group :Esketamine,electrodes were placed
TEAS+Esketamine Group :TEAS+Esketamine

Sponsors

Xuzhou Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective surgery 2. Age: >18 years old 3. American Society of Anesthesiologists (ASA) grade I-III 4. BMI 18.5 kg/m2-28 kg/m2

Exclusion criteria

Exclusion criteria: 1. Pittsburgh Sleep Quality Index score >7 2. Sleep apnea, or moderate or more severe snoring 3. Patients with severe sinus bradycardia (heart rate lower than 50 beats per minute) or sinoatrial node lesions, second or third degree atrioventricular block, with pacemaker 4. Patients taking anticonvulsants, antidepressants or other psychotropic drugs for a long time 5. Patients with high sensitivity or allergy to the drugs or devices used in this study 6. Patients with severe heart, liver or kidney disease 7. Patients who have participated in other clinical trials within the past 3 months 8. Patients with hearing and language disorders, unable to communicate effectively with the physician 9. Patients who are pregnant or breastfeeding 10. Patients with fever or infection before surgery 11. Patients who live with critically ill patients or more than 3 people in the same ward 12. Patients at risk of increased intracranial pressure, uncontrolled or poorly controlled hypertension 13. Hyperthyroidism

Design outcomes

Primary

MeasureTime frame
HRV;sleep quality;depression scores;

Secondary

MeasureTime frame
NRS scores;Duration of surgery;

Countries

Chnia

Contacts

Public ContactLu Feifei

Xuzhou TCM Hospital

lufei09flg@126.com+86 516 6869 3127

Outcome results

None listed

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