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The study for acupoint stimulation on preventive treatment of advenocortical function inhibition induced by etomidate: a randomized, double-blind, prospective study.

The study for acupoint stimulation on preventive treatment of advenocortical function inhibition induced by etomidate: a randomized, double-blind, prospective study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000041545
Enrollment
Unknown
Registered
2020-12-28
Start date
2021-01-01
Completion date
Unknown
Last updated
2021-03-15

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

Conditions

advenocortical function inhibition

Interventions

Sponsors

The Second Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: Patients must meet all of the following criteria for inclusion in this study: 1. Aged 18-90 years, gender unlimited; 2. ASA range from I to III grade; 3. 18 kg/m2<BMI<30kg/m2; 4. Clear understanding and voluntary participation in this study.

Exclusion criteria

Exclusion criteria: 1. Patients with endocrine system diseases such as Kuxing syndrome, pituitary adenoma and adrenal tumor; 2. Patients with hormone drugs within 3 months before operation; 3. Patients with glucocorticoid drugs intraoperatively and postoperatively; 4. Asthma patients; 5. Severe respiratory diseases (obstructive sleep apnea syndrome, acute respiratory infection, acute attack of chronic obstructive pulmonary disease, uncontrolled asthma, active massive hemoptysis, severe pulmonary hypertension, etc); 6. Acute heart failure; unstable angina pectoris; myocardial infarction within 6 months before screening; resting electrocardiogram heart rate = 450 ms, female >= 470ms; patients with aortic aneurysm; 7. Infectious heart diseases such as myocarditis or endocarditis; septicemia; 8. People with mental system diseases (schizophrenia, mania, bipolar disorder, insanity, etc.) and long-term history of taking psychotropic drugs and cognitive impairment; 9. Anemia or thrombocytopenia: Hb ULN +3s and/or APTT > ULN+10s; 11. Liver dysfunction: AST and/or ALT >= 2.5 x ULN, TBIL >= 1.5 x ULN; 12. Renal dysfunction: urea or urea nitrogen >= 1.5x ULN, serum creatinine greater than the upper limit of normal value; 13. There was a history of substance abuse, drug abuse and alcohol abuse within two years prior to the screening period, with alcohol consumption, i.e. drinking more than 2 units of alcohol per day on average (1 unit =360 ml beer or 45 ml liquor with 40% alcohol or 150 wine); 14. Patients who did not receive regular hypotension or have poor blood pressure control (sitting systolic blood pressure >= 160 mmHg or 90 mmHg, and / or 100 mmHg diastolic blood pressure during screening); 15. Patients whose blood glucose was not satisfactorily controlled (random blood glucose >= 11.1 mmol/l); 16. Allergic or contraindicated drugs such as benzodiazepines, opioids, etomidate, propofol and their components; 17. Patients identified as having difficulties in respiratory management (modified Mallampati ? grade); 18. Participated in any clinical drug trial and used the trial drug as a subject in the last 3 months; 19. Patients who could undergo adrenal surgery; 20. Contraindications of trauma and infection in acupuncture and moxibustion puncture site; 21. Other factors that may interfere with the results.

Design outcomes

Primary

MeasureTime frame
Concentration of Serum cortisol;

Secondary

MeasureTime frame
Duration of patients' consciousness recovery;Duration of Tracheal tube withdrawal;Duration of staying in PACU;Postoperation nausea and vomitting times;Excessive sedation;POCD;Incidence of fever;Postoperative recovery time of gastrointestinal function;Chalder fatigue rating scaleChiari;

Countries

China

Contacts

Public ContactSiyuan Li

The Second Affiliated Hospital of Xi'an Jiaotong University

347585731@qq.com+86 18681875961

Outcome results

None listed

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