Beijing Tiantan Hospital
Beijing, Beijing Municipality, 100070, China
Location status: Recruiting
NCT Number: NCT07028190
To compare the dosage requirement of rimazolen under intravenous anesthesia between patients with insomnia and those with normal sleep pattern.
Interested in participating?
Request Info18 year–64 year
All sexes
Observational
Beijing, Beijing Municipality, 100070, China
Location status: Recruiting
The investigators aim to investigate whether rimazolen dosage requirement is increased in patients with insomnia under intravenous anesthesia compared with normal sleep patterns.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
No interventions, this study is to compare the dosage requirement of ciprofol under intravenous anesthesia between insomnia group and normal sleep group.
Time frame: Up to 1 day
The total consumption of rimazolen for the produre. It includes the total amount of ciprofol required by the patient for the entire procedure.
Time frame: 1 day
The dosage of rimazolen for induction of anesthesia
Time frame: The day of the procedure and 24 hours after the procedure
The occurrence of the respiratory and cardiovascular adverse events such as hypoxemia, hypotension, hypertension, arrhythmia
Time frame: The day of the procedure and 24 hours after the procedure
The occurrence of the other adverse events such as dizziness, agitation, nausea, vomiting and psychiatric symptom
Time frame: The day of the procedure and 24 hours after the procedure
The patient is conscious after anesthesia
Time frame: Up to 1 day
The time from when the patient stops intravenous anesthetic drug application to when they can open their eyes and nod their heads.
Time frame: Up to 1 day
Patients' stay time in PACU
Time frame: Up to 1 day
The ease of operation at this level of sedation (easy/medium/difficult) evaluated by the operation doctors
Time frame: Up to 1 day
The satisfaction degree of anesthesia effect (satisfactory/medium/unsatisfactory) evaluated by the operation doctors
Time frame: Up to 1 day
Patients' satisfaction with the procedure at this level of sedation (satisfactory/medium/unsatisfactory)
Time frame: Up to 1 day
Patients' willingness to undergo the next procedure at the same level of sedation. Patient willingness is divided into three levels: willing, moderate, and unwilling.
Beijing Tiantan Hospital
Other
Changes in Rimazolen Dosage in Patients With Insomnia Under Intravenous Anesthesia: a Prospective Cohort Study
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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