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Study on correlation between painless gastroscopic hiccup and ramazolam injection rate

Study on correlation between painless gastroscopic hiccup and ramazolam injection rate

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076912
Enrollment
Unknown
Registered
2023-10-24
Start date
2023-04-25
Completion date
Unknown
Last updated
2023-10-30

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

Conditions

Hiccup

Interventions

Group A:Remazolam 5mg at a rate of 15S and propofol 1.0 mg/kg
Group B:Remazolam 5mg at a rate of 30S and propofol 1.0 mg/kg
Group C:Remazolam 5mg at a rate of 45S and propofol 1.0 mg/kg
Group D:Remazolam 5mg at a rate of 60S and propofol 1.0 mg/kg
Group E:Group E was only induced by 2.0 mg/kg propofol without remazolam intervention

Sponsors

The Second Affiliated Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1)Age 20-65 years old; (2) Gender is not limited; (3)American Society of Anesthesiologists (ASA) Level I to II; (4) The body mass index (BMI) is 18.0-24.0 kg/m2.

Exclusion criteria

Exclusion criteria: (1) Patients with difficult airway (neck mobility limited, Mallampati grades 3-4, nappe-chin distance <6cm), basal SpO2<90%, or sleep apnea syndrome; (2) long-term use of sedative hypnotic patients; (3) Patients with contraindications of benzodiazepines, opioids and propofol; (4) Changes in endoscopy caused by gastrointestinal bleeding, gastrointestinal perforation, etc.

Design outcomes

Primary

MeasureTime frame
Hiccup;

Secondary

MeasureTime frame
Time of onset of anesthesia;Endoscopic operation time;

Countries

China

Contacts

Public ContactHaitao Yang

The Second Affiliated Hospital of Dalian Medical University

1643148967@qq.com+86 155 4117 8529

Outcome results

None listed

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