Actively Recruiting
Changes in Etomidate Dosage in Insomnia Patients Undergoing Digestive Endoscopy
Led by Beijing Tiantan Hospital · Updated on 2025-09-10
840
Participants Needed
1
Research Sites
93 weeks
Total Duration
On this page
Sponsors
B
Beijing Tiantan Hospital
Lead Sponsor
D
Daxing Teaching Hospital, Capital Medical University
Collaborating Sponsor
AI-Summary
What this Trial Is About
To compare the dosage requirement of etomidate during digestive endoscopy between patients with insomnia and those with normal sleep pattern.
CONDITIONS
Official Title
Changes in Etomidate Dosage in Insomnia Patients Undergoing Digestive Endoscopy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 64 years
- American Society of Anesthesiologists (ASA) physical status I or II
- Body mass index (BMI) between 15 and 30
- Scheduled for digestive endoscopy under intravenous anesthesia
- For insomnia group: positive diagnosis of insomnia disorder based on DSM-5 criteria and a Sleep Condition Indicator score of 16 or less
- For normal sleep group: no history or evidence of insomnia
You will not qualify if you...
- Presence of any neurological disease
- Daily alcohol consumption
- Contraindications to intravenous anesthetic drugs, such as hypotension or shock
- History of allergy to any drug used in the study
- Pregnancy or breastfeeding
- Diagnosis of sleep apnea syndrome
- Acute upper respiratory infection
- Psychological diseases with reported suicidal thoughts
- Frequent night-time responsibilities for work or caregiving
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Beijing Tiantan Hospital
Beijing, Beijing Municipality, China, 100070
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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