Trials / Recruiting
RecruitingNCT07028190
Changes in Rimazolen Dosage in Insomnia Patients Undergoing Digestive Endoscopy
Changes in Rimazolen Dosage in Insomnia Patients Undergoing Digestive Endoscopy: a Prospective Cohort Study
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 840 (estimated)
- Sponsor
- Beijing Tiantan Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 64 Years
- Healthy volunteers
- Not accepted
Summary
To compare the dosage requirement of rimazolen during digestive endoscopy between patients with insomnia and those with normal sleep pattern.
Detailed description
The investigators aim to investigate whether rimazolen dosage requirement is increased in patients with insomnia undergoing digestive endoscopy compared with normal sleep patterns.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | No interventions, it is a observational study | No interventions, this study is to compare the dosage requirement of ciprofol during digestive endoscopy between insomnia group and normal sleep group. |
Timeline
- Start date
- 2025-06-12
- Primary completion
- 2027-03-31
- Completion
- 2027-03-31
- First posted
- 2025-06-19
- Last updated
- 2025-09-10
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT07028190. Inclusion in this directory is not an endorsement.