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Application of Remazolam Besylate Combined with Esketamine in Painless Gastroenteroscopy Diagnosis and Treatment of Overweight/Obese Patients: A Prospective Randomized Controlled Study

Application of Remazolam Besylate Combined with Esketamine in Painless Gastroenteroscopy Diagnosis and Treatment of Overweight/Obese Patients: A Prospective Randomized Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083833
Enrollment
Unknown
Registered
2024-05-06
Start date
2024-05-10
Completion date
Unknown
Last updated
2024-05-13

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

Conditions

Hypoxemia

Interventions

control group:Intravenous injection of propofol and ketamine
treatment group:Intravenous injection of Remazolam Besylate and Esketamine

Sponsors

The Second People's Hospital of Shenzhen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Patients who plan to undergo painless digestive endoscopy examination and diagnosis and treatment; (2) Patients aged = 18 years old; (3) Body mass index (BMI) = 25 kg/m ²; (4) The American Society of Anesthesiologists (ASA) is classified as Grade II-III. (5) The subjects voluntarily participate and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients who refuse to participate in the trial; (2) Individuals with a history of severe heart, brain, lung, liver, kidney, and metabolic diseases; (3) Within 2 weeks, there is a history of acute respiratory inflammation that has not been cured; (4) Preoperative systolic blood pressure in hypertensive patients = 180mmHg and/or diastolic blood pressure = 110mmHg, or hypotension patients<90/60mmHg; (5) Individuals with neuromuscular system diseases or mental illnesses; (6) Suspected misuse of anesthetic analgesics or sedatives; (7) Individuals who are allergic to drugs such as propofol, ketamine, and remrazolam besylate; (8) Those who are uncooperative and unable to communicate.

Design outcomes

Primary

MeasureTime frame
The incidence of hypoxemia;

Secondary

MeasureTime frame
Absolute value of pulse oxygen saturation;Mean arterial pressure;heart rate;respiratory rate;BIS value;inspection time;Wake-up time;Time of leaving the recovery room;MOAA/S scores;CAM scores;Dosage of Remazolam Benzenesulfonate;Dosage of propofol;Adverse reaction occurrence;

Countries

China

Contacts

Public ContactYang Han

The Second People's Hospital of Shenzhen

13798509@qq.com+86 158 9977 8910

Outcome results

None listed

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