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Comparison of clinical effect of cipofol combined with remifentanil and etomidate combined with remifentanil in elderly patients with painless gastroscopy

Comparison of clinical effect of cipofol combined with remifentanil and etomidate combined with remifentanil in elderly patients with painless gastroscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087849
Enrollment
Unknown
Registered
2024-08-06
Start date
2024-08-07
Completion date
Unknown
Last updated
2024-08-12

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

Conditions

Digestive system diseases

Interventions

Group C:Remifentanil was injected intravenously with 0.2-0.4ug/kg (drug concentration 2ug/ml) for 30± 5 s, and was timed from the beginning. After 1 min, group C was injected intravenously with 0.2-0.
Group E:Remifentanil was injected intravenously with 0.2-0.4ug/kg (drug concentration 2ug/ml) and the infusion time was 30± 5 s. The infusion time was 30± 5 s from the beginning. After 1 min, etomidat

Sponsors

Yibin Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Age 60-80 years old. 2.ASA is graded from I to II. 3. Painless gastroscopy (within 20 minutes). 4.BMI:18~30kg/?. 5.Fried frailty Assessment Scale (?2 items).

Exclusion criteria

Exclusion criteria: 1. Patients and their families refused to participate in the study; 2. Allergic or contraindicated to opioids, cyclopofol, etomidate and other drugs and their components; 3. Patients with hypertension who did not receive formal antihypertensive treatment before surgery or whose blood pressure was poorly controlled [SBP= 160 mm Hg or =90 mm Hg, and/or DBP=100 mm Hg]; Preoperative BMI>30 or < 18 kg/?; Patients with severe anemia, hypotensive shock; 4. Patients with severe cardiopulmonary diseases, liver and kidney dysfunction, adrenal insufficiency, apnea syndrome, and modified Mallampati grade IV; 5. Patients with full stomach, digestive tract obstruction and progressive digestive tract bleeding; Recent use of antipsychotic drugs, drug abuse; 6. Patients with bronchial asthma, AECOPD, myasthenia gravis, severe mental illness, language and communication disorders; 7. Patients with a history of drug abuse, alcoholism, or drug addiction, and patients who have participated in other clinical trials as subjects within the last 3 months.

Design outcomes

Primary

MeasureTime frame
Incidence of respiratory adverse reactions;

Secondary

MeasureTime frame
Success rate of gastroscopy;Incidence of nausea and vomiting;Doctor and patient satisfaction evaluation;Incidence of muscle fibrillation;Success rate of gastroscopy insertion;Incidence of cough;Body motion rate;Incidence of sedation recovery;Incidence of injection pain;

Countries

China

Contacts

Public Contactshen chunhong

Yibin Second People's Hospital

377417689@qq.com+86 152 9818 4772

Outcome results

None listed

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