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Application of intravenous Cipofol combined with low-dose alfentanil in painless transesophageal echocardiography in outpatient settings

The safety and efficacy study of Propofol-Fentanyl and Remifentanil-Fentanyl in outpatient painless transesophageal echocardiography

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081723
Enrollment
Unknown
Registered
2024-03-11
Start date
2024-03-13
Completion date
Unknown
Last updated
2024-03-18

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

Conditions

Cardiac disease

Interventions

Ciprofol group:Intravenous bolus injection of 5ug/kg of alfentanil, followed by slow injection (30 seconds) of 0.5mg/kg of Cipofol for anesthetic sedation during transesophageal echocardiography.
Proprofol group:Intravenous bolus injection of 5ug/kg of alfentanil, followed by slow injection (30 seconds) of 2mg/kg of Propofol for anesthetic sedation during transesophageal echocardiography.

Sponsors

Xiamen Cardiovascular Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Ages 18-90 years (2) Have indications for painless transesophageal echocardiography (3) Patients with good cognitive status (4) Body mass index (BMI) of 18-30kg/m2 (5) Normal liver and kidney function

Exclusion criteria

Exclusion criteria: (1) Emergent surgery (2) ASA class V patients (3) Patients with clinically diagnosed coagulation disorders, severe liver or kidney impairment(4) History of upper gastrointestinal bleeding within the past three months(5) Abnormalities in the esophagus or stomach, or history of related surgeries (6) History of psychiatric disorders or long-term use of analgesic drugs (7) Left ventricular ejection fraction (EF) <25% (8) Inability to cooperate with the study for any reason, such as language comprehension, mental illness, inability to travel to the study center, etc. (9) Use of other investigational drugs or participation in other clinical trials within the 3 months prior to enrollment(10) The investigator deems that inclusion in this trial is not appropriate.

Design outcomes

Primary

MeasureTime frame
Adverse events related to sedation;Cough reflex;

Secondary

MeasureTime frame
Body's movements;Pain upon intravenous injection;

Countries

China

Contacts

Public ContactGuoshengwen, Yanpianpian, Jianglulu

Xiamen Cardiovascular Hospital

fwguoshengwen@163.com+86 1511854057

Outcome results

None listed

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