Anesthesia, Hemodynamics, Postoperative Recovery
Conditions
Keywords
Ciprofol, Hemodynamics, Postoperative Recovery, propofol
Brief summary
To study the Effect of Ciprofol Infusion for Induction and Maintenance of anesthesia on Hemodynamics and Postoperative Recovery in Patients Undergoing Thoracoscopic Lobectomy:a randomized, controlled trial.
Detailed description
Patients undergoing Thoracoscopic Lobectomy aged 18\ 65 years old were randomly assigned to Group P and Group C . Group P was given propofol 2 \ 2.5mg/kg, group C was given ciprofol 0.4 \ 0.5mg/kg, if bispectral index(BIS) value ≤60 during anesthesia induction, cisatracurium 0.2mg/kg and sufentanil 0.5μg/kg were injected intravenously, endotracheal intubation was performed after the improvement of muscle relaxation. If the BIS value was greater than 60, propofol was added intravenously 1mg/kg each time or ciprofol 0.2mg/kg each time, and the interval of administration was greater than 1min, until BIS≤60. Cisatracurium and sufentanil were injected intravenously, followed by endotracheal intubation.Then propofol was maintained in group P at 4-12 mg/kg/h and remifentanil was maintained at 0.1-0.3 ug/kg/min .Ciprofol was maintained in Group C at 0.8-2.5 mg/kg/h and remifentanil was maintained at 0.1-0.3 ug/kg/min . Intermittent addition of cisatracurium. Sufentanil was added as required, and total dosage of Sufentanil was 0.7ug \ 1ug/kg. BIS was kept at 40 \ 60 during the surgery, and infusion drugs were stopped at the end of the operation. The patients were Transfer to Postanesthesia care unit(PACU) after the operation. The primary outcomes were the fluctuations in hemodynamic parameters during induction and the surgery. Systolic blood pressure (SBP), diastolic blood pressure (DBP), mean blood pressure (MAP),heart rate (HR) and BIS values at various time points were collected. The secondary outcome were as follows: 1. The time of lose consciousness（LOC） during the induction, The Time and dosage of additional drug, and the BIS value during the induction process. 2. The incidence of adverse events such as injection pain, body movement, muscle twitching, hypotension, hypertension, bradycardia or tachycardia, cough and bronchospasm during induction. 3. quality of recovery 15（QOR15） score at pre-operation（Preop） 、on the first day of postoperation （POD1）and on the second day of postoperation （POD2） . 4. the recovery time of consciousness (ROC）, extubation time, PACU stay time, postoperative hospital stay time. 5. Incidence of postoperative nausea and vomiting, incidence of postoperative agitation and delayed recovery, and intraoperative awareness.
Interventions
DRUGpropofol
propofol 2～2.5mg/kg was used for anesthesia induction. propofol is an intravenous sedative-hypnotic and a short-acting GABAA receptor agonist. It activates GABAergic neurons by enhancing chloride ion influx. It is used for anesthesia of induction and maintenance.
DRUGciprofol
Ciprofol 0.4～0.5mg/kg was used for anesthesia induction. Ciprofol is an intravenous sedative-hypnotic and a short-acting GABAA receptor agonist. It activates GABAergic neurons by enhancing chloride ion influx. It is used for anesthetic induction and maintenance agents include rapid induction of general anesthesia, rapid recovery of consciousness, minimal residual effects on the central nervous system and less injection pain.
Sponsors
Xiumei Song
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No
Inclusion criteria
* American Society of Anesthesiology (ASA)Ⅰ～Ⅱ grade; * 18-65 years; * Body mass index (BMI) 20-30kg/m2 ; * Scheduled for thoracoscopic lobectomy under general anesthesia;
Exclusion criteria
* Refused to participate in the clinical study; * Predictable airway difficulties requiring awake intubation; * Allergy to the drugs which were used in this study; * Tracheal intubation failed for twice; * Patients with mental diseases or consciousness disorder; * long-term use of sedatives or Antidepressants; * Patients who are participating in other clinical studies.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Hemodynamic fluctuations: Systolic blood pressure(SBP) | during anesthesia induction，perioperative | Systolic blood pressure(SBP) during anesthesia induction and surgery. |
| Hemodynamic fluctuations: Diastolic blood pressure(DBP) | during anesthesia induction，perioperative | Diastolic blood pressure(DBP) during anesthesia induction and surgery. |
| Hemodynamic fluctuations: mean blood pressure (MAP) | during anesthesia induction，perioperative | MAP during anesthesia induction and surgery. |
| Hemodynamic fluctuations: Heart rate (HR) | during anesthesia induction，perioperative | Heart rate (HR) during anesthesia induction and surgery. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The time of lose consciousness（LOC） during the induction | during anesthesia induction | The time of lose consciousness（LOC） during the induction was defined as from the drug was administered until the patients loss of consciousness(when the BIS≤60) |
| Incidence of intraoperative awareness | 2 hours after surgery | Brice Questionnaire was used to assess the occurrence of intraoperative awareness. |
| The incidence of adverse events during induction | during induction | The incidence of adverse events such as injection pain, body movement, muscle twitching, hypotension, hypertension, bradycardia or tachycardia, cough and bronchospasm during induction. |
| quality of recovery | pre-operation, postoperation of day 1 ,postoperation of day2 | quality of recovery 15（QOR15） score at pre-operation（Preop） 、 postoperation day 1 ,postoperation of day2 |
| postoperative recovery | 2 hours after surgery | Incidence of postoperative nausea and vomiting was record use Classification of nausea and vomiting |
Countries
China
Contacts
Primary ContactNA GUO, Doctor
Outcome results
None listed