Status:

NOT_YET_RECRUITING

Network Pharmacology Was Applied to Explore the Mechanism of Remimazolam Applied in General Anesthesia for Gynecological Surgeries

Lead Sponsor:

Second Hospital of Shanxi Medical University

Conditions:

Gynecological Disease

Eligibility:

FEMALE

18-64 years

Phase:

NA

Brief Summary

To explore the related mechanisms by which remimazolam regulates hemodynamic stability, inflammatory factors and the immune system in patients undergoing general anesthesia for gynecological surgeries...

Detailed Description

①Clinical effect evaluation of remimazolam 1. Compare the hemodynamic stability (heart rate, mean arterial pressure, blood oxygen saturation), anesthesia efficiency (induction time, recovery time), a...

Eligibility Criteria

Inclusion

  • The patient or their family members sign the informed consent form
  • Age: 18-64 years old, BMI: 18-30kg/m2
  • ASA Grade Ⅰ or Ⅱ
  • Patients undergoing gynecological surgeries (laparoscopic total hysterectomy, adnexectomy and myomectomy)

Exclusion

  • People who are allergic to remimazolam or benzodiazepinesThyroid disease
  • Long-term use of benzodiazepines
  • Pregnancy or lactation
  • Have a history of drug abuse or alcoholism
  • Patients with contraindications for surgery
  • Patients with hypertension (clinically diagnosed with hypertension) and patients with coronary heart disease (with typical angina pectoris symptoms and excluding aortic valve lesions, with a clear history of old myocardial infarction, with a clear history of acute myocardial infarction, and CAG finding coronary artery stenosis greater than or equal to 70%)
  • Patients with arrhythmia, heart failure, renal failure, and those who have recently taken cardiovascular active drugs
  • Endocrine disorders such as hyperthyroidism and pheochromocytoma that may affect the hemodynamic level of the body
  • Patients with ketoacidosis and lactic acidosis
  • Abnormal liver function, ALT\> three times the upper limit of the normal value;
  • Renal failure (serum creatinine \>3mg/dl or creatinine clearance rate \<30ml/min)
  • Patients who have been using sedatives or antidepressants for a long time, or have a history of alcohol abuse or drug dependence
  • Asthma or reactive airway diseases
  • Combined with underlying cognitive function abnormalities
  • Exclusion criteria for research subjects
  • Those who were mistakenly included without meeting the inclusion criteria
  • Those who experienced adverse events such as shock, severe hypotension and severe arrhythmia during the operation

Key Trial Info

Start Date :

June 1 2025

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

January 1 2026

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT06990763

Start Date

June 1 2025

End Date

January 1 2026

Last Update

May 25 2025

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