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Changes in Ciprofol Dosage in Insomnia Patients Undergoing Digestive Endoscopy

NCT06897007 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 840

Last updated 2025-09-10

No results posted yet for this study

Summary

To compare the dosage requirement of ciprofol during digestive endoscopy between patients with insomnia and those with normal sleep pattern.

Conditions

Interventions

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.

Sponsors & Collaborators

  • Daxing Teaching Hospital, Capital Medical University

    collaborator UNKNOWN

  • Hebei Medical University Third Hospital

    collaborator OTHER

  • Hengshui People's Hospital

    collaborator OTHER

  • Beijing Tiantan Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
64 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-03-24
Primary Completion
2027-03-31
Completion
2027-03-31

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06897007 on ClinicalTrials.gov