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Clinical observation of remimazolam tosylate combined with low-dose propofol in painless gastroscopy

Clinical observation of remimazolam tosylate combined with low-dose propofol in painless gastroscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051453
Enrollment
Unknown
Registered
2021-09-23
Start date
2021-10-01
Completion date
Unknown
Last updated
2022-06-20

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

Conditions

painless gastroscopy

Interventions

Control group1:only remimazolam tosylate was used
Control group2:only propofol was used
Experimental group:remimazolam tosylate and propofol were given successively

Sponsors

The First People's Hospital of Jingzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. The clinical data are accurate and complete, and patients who plan to undergo painless gastroscopy diagnosis and treatment; 2. Aged 18 to 60 years, BMI 18-28Kg/m2, ASA grade I-II; 3. No dysfunction of important organs such as heart, lung, liver and kidney, and no shock; 4. Have reading and comprehension skills, be informed about this research, and participate voluntarily.

Exclusion criteria

Exclusion criteria: 1. Patients with obvious respiratory and circulatory dysfunction and abnormal liver and kidney function before surgery; 2. Patients with severe neuropsychiatric diseases, long-term use of psychotropic drugs and cognitive dysfunction; 3. Those suffering from infectious diseases; 4. Those who have taken benzodiazepines or opioids intermittently every day within 1 month or within the past 3 months; 5. Those who are allergic or contraindicated to benzodiazepines, opioids, propofol, flumazenil, naloxone and other drugs and their components; 6. Obesity, OSAS and other patients who are judged to have difficulty in airway management: modified Markov score grade III and above; 7. History of drug abuse, and history of severe alcoholism; 8. Pregnant or breastfeeding women, or family planning within 3 months (including men); 9. Participate in any clinical trial within the past 3 months.

Design outcomes

Primary

MeasureTime frame
Incidence of perioperative adverse effects;

Secondary

MeasureTime frame
the induction time of sedation;time to alert;time to discharge;

Countries

China

Contacts

Public ContactXia Rui

The First People's Hospital of Jingzhou

879560350@qq.com+86 18972161338

Outcome results

None listed

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