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Individualized medication guidance of anesthesia for obese patients by human component analysis

Individualized medication guidance of anesthesia for obese patients by human component analysis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200056598
Enrollment
Unknown
Registered
2022-02-08
Start date
2022-04-10
Completion date
Unknown
Last updated
2024-10-21

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

Conditions

Obesity

Interventions

Remazolam group 1:Low dose Remazolam
Remazolam group 2:Medium dose Remazolam
Remazolam group 3:High dose Remazolam
Alfentanil group 1:Low dose Alfentanil
Alfentanil group 2:Medium dose Alfentanil
Alfentanil group 3:High dose Alfentanil
Esmketamine group 1:Low dose Esmketamine
Esmketamine group 2:Medium dose Esmketamine
Esmketamine group 3:High dose Esmketamine

Sponsors

He'nan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients who intend to undergo painless gastroenteroscopy; 2. Aged 18-65 years, no gender limit; 3. Body fat percentage (PBF) >20% in males and >28% in females; 4. American Society of Anesthesiologists (ASA) Grade I-III.

Exclusion criteria

Exclusion criteria: 1. Patients who refused to participate in the trial; 2. Patients with a history of severe heart, brain, lung, liver, kidney and metabolic diseases; 3. Patients with previous abnormal surgical anesthesia recovery history; 4. Electrocardiogram: heart rate 180mmHg and/or diastolic blood pressure >110mmHg in hypertensive patients, or < 90/60mmHg in hypotensive patients; 7. Patients with neuromuscular system diseases or mental diseases; 8. Anemia patients; 9. Suspected abuse of narcotic analgesics or sedatives; 10. Those who are predicted to have or have had difficult airway; 11. Known allergy to emulsions and opioids; 12. Uncooperative and unable to communicate.

Design outcomes

Primary

MeasureTime frame
Incidence of respiratory depression;

Secondary

MeasureTime frame
Vital signs;Effectiveness index;Ramsay sedation score;BPS - NI behavior improved pain rating scale;

Countries

China

Contacts

Public ContactLiu Shengqun

He'nan Provincial People's Hospital

13526882118@163.com+86 13526882118

Outcome results

None listed

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