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A domestic and prospective study of rimazole for injection in digestive endoscopy

A domestic and prospective study of rimazole for injection in digestive endoscopy

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200064794
Enrollment
Unknown
Registered
2022-10-18
Start date
2022-11-01
Completion date
Unknown
Last updated
2023-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

gastrointestinal endoscopy andObstructive jaundice

Interventions

Queue I:None
Queue II:None
Jaundice group:Using Dixon and Massey sequential distribution test formula to calculate the dosage of rimazole

Sponsors

Tianjin Nankai hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients who used rimazole for painless gastroscopy sedation and painless colonoscopy sedation; 2. Patients with obstructive jaundice (serum tbl>17.1 µ mol/L) treated with rimazole for painless endoscopic sedation.

Exclusion criteria

Exclusion criteria: 1. Patients who are participating or planning to participate in any intervention clinical trial; 2. The investigator believes that there are any other reasons that make the patient unsuitable to participate in this study; 3. Patients using other analgesic or neuroleptic drugs; 4. Patients who suffered from heart, lung, kidney or metabolic diseases; 5. The data of patients who have not signed the informed consent form will not be included and will be removed from the database.

Design outcomes

Primary

MeasureTime frame
Safety and success rate of remidazolam in sedation by gastroscopy and colonoscopy;Incidence of hypotension and respiratory depression;Sensitivity of remazolam in patients with obstructive jaundice, ED50 and ED95;

Countries

China

Contacts

Public ContactMu Rui

Tianjin Nankai hospital

muruimurui@sina.com+86 13672036727

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026