Skip to content

Anesthesia of elderly patients with ERCP based on ERAS concept using esketamine combined with propofol TCI: A prospective randomized controlled study

Anesthesia of elderly patients with ERCP based on ERAS concept using esketamine combined with propofol TCI: A prospective randomized controlled study

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072850
Enrollment
Unknown
Registered
2023-06-27
Start date
2023-06-27
Completion date
Unknown
Last updated
2023-07-02

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

Conditions

Diseases of the biliary and pancreatic ducts

Interventions

E:Esketamine is maintained at 0.15mg/kg/h after 0.15mg/kg/h intravenously
R:Pump refentanil 0.025ug/kg/min to maintain
D:The injection load of dexmedetomidine pump is 0.5ug/kg and maintained at 0.5ug/kg/h after 10min

Sponsors

Shanghai Putuo District Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patient's age= 60 years old; 2. American Association of Anesthesiologists Anesthesia Grade: Grade I-III; 3. Those who have indications for surgery; 4. Those with normal liver and kidney function; 5. Those with normal coagulation function; 6.Patients and families voluntarily sign informed consent forms.

Exclusion criteria

Exclusion criteria: 1. Those with infectious diseases and blood system diseases; 2. Those with elevated blood lactate or metabolic disorders; 3. Patients with end-stage chronic diseases, active bleeding, severe pulmonary hypertension, heart failure and acute myocardial infarction; 4. Those with a history of contraindications to surgery; 5. Those with a history of contraindications to anesthesia; 6. Accompanied by serious infection and abnormal function of important organs (heart, brain, lung, etc.); 7. Those who cannot cooperate with researchers due to mental disorders or mental illness.

Design outcomes

Primary

MeasureTime frame
Hemodynamics;Respiratory mechanics;Regulation of visceral autonomic function;Cognitive function in patients after anesthesia;Perioperative blood tests;

Secondary

MeasureTime frame
CAM scores were performed 24 h postoperatively, 48 h postoperatively, and 72 h postoperatively;Pittsburgh sleep quality index (PSQI) 1d before and 72h after surgery;Evaluation of surgeon and patient satisfaction;Surgery time, end of operation to BIS value> 85 awakening time;Aldrete scored > 9 for resuscitation room time;Total propofol;Number of nausea and vomiting in the patient;

Countries

China

Contacts

Public ContactJuan lV

Shanghai Putuo District Central Hospital

Juanlvdream@163.com+86 158 2183 9097

Outcome results

None listed

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