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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06009055
Other study ID # hanyi20230117
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 17, 2023
Est. completion date December 31, 2024

Study information

Verified date January 2024
Source Second Hospital of Shanxi Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The patients with diabetes who underwent laparoscopic cholecystectomy in the general surgery department of the Second Hospital of Shanxi Medical University were selected. The patients who were induced by remimazolam were included in the experimental group, and the patients who were induced by propofol were included in the control group. All the selected patients had no intimate relationship. The differences of blood pressure, heart rate and heart rate variability (HRV) between the experimental group and the control group were observed. According to the literature, it is speculated that the changes of blood pressure, heart rate and HRV indexes in the experimental group are smaller than those in the control group, and the difference is statistically significant.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date December 31, 2024
Est. primary completion date November 30, 2024
Accepts healthy volunteers No
Gender All
Age group 30 Years to 70 Years
Eligibility Inclusion Criteria: - Diagnosed as type 2 diabetes according to the "Chinese Guidelines for the Prevention and Treatment of Type 2 diabetes 2020" - ASA II or III Exclusion Criteria: - People who are allergic to Remimazolam - It is estimated that patients with difficulty in tracheal intubation (poor head and neck mobility, history of airway surgery, history of OSAHS, nail to chin distance<6cm, Malampati grade 3 and above, mouth opening<2.5cm, obesity (BMI>30kg ยท m-2), etc - Hypertension (clinically diagnosed as hypertension) - Patients with coronary heart disease (with typical symptoms of angina pectoris and exclusion of aortic valve disease, clear history of old myocardial infarction, clear history of acute myocardial infarction, coronary stenosis greater than or equal to 70% found by CAG) - Patients with arrhythmia, heart failure, renal failure, and recently taking cardiovascular active drugs - Endocrine diseases such as hyperthyroidism and pheochromocytoma that may affect the level of body hemodynamics - Ketoacidosis and lactic acidosis - Patients with long-term use of sedatives or antidepressants or a history of alcoholism or drug dependence - Asthma or reactive airway disease - Patients with myasthenia gravis and cognitive dysfunction cannot cooperate with this study

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Remimazolam
0.3mg/kg,injection completed in 30 seconds
Propofol
2mg/kg,injection completed in 30 seconds

Locations

Country Name City State
China econd of Shanxi Medical University Taiyuan Shanxi

Sponsors (1)

Lead Sponsor Collaborator
Zheng Guo

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary systolic pressure (SBP) Changes in systolic blood pressure 24 hours
Primary diastolic pressure(DBP) change of diastolic blood pressure 24 hours
Primary heart rate change of heart rate 24 hours
Primary Heart rate variability(HRV) Changes of various indicators of heart rate variability 24 hours
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