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The effect of esketamine combined with dexmedetomidine on the quality of postoperative recovery in patients undergoing laparoscopic hernia repair

The effect of esketamine combined with dexmedetomidine on the quality of postoperative recovery in patients undergoing laparoscopic hernia repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400086479
Enrollment
Unknown
Registered
2024-07-02
Start date
2024-07-11
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Abdominal hernia

Interventions

Group 0.3: 0.3 mg/kg esketamine will be used during anesthesia induction and the maintenance dose is 0.3 mg/kg/h during the operation.
Group 0.4: 0.4 mg/kg esketamine will be used during anesthesia induction and the maintenance dose is 0.4 mg/kg/h during the operation.
Group 0.5: 0.5 mg/kg esketamine will be used during anesthesia induction and the maintenance dose is 0.5 mg/kg/h during the operation.
Group 0.6: 0.6 mg/kg esketamine will be used during anesthesia induction and the maintenance dose is 0.6 mg/kg/h during the operation.
Group 0.7: 0.7 mg/kg esketamine will be used during anesthesia induction and the maintenance dose is 0.7 mg/kg/h during the operation.
Group of esketamine ( Group K ):Anesthesia will be induced and maintained with an ED 50 dose of esketamine.
Group of opioids ( Group C ): 0.6 ug/kg sufentanil will be used during anesthesia induction and 0.1-0.3 ug/kg/h remifentanil will be used for anesthesia maintenance.

Sponsors

Anqing Municipal Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective laparoscopic herniorrhaphy; 2. Patients over 18 years old; 3. American Society of Anesthesiologists(ASA) Physical Status I-II; 4. New York Heart Association (NYHA) cardiac function is graded I-II; 5. Body Mass Index (BMI) is 18-30 kg/m2.

Exclusion criteria

Exclusion criteria: 1. Patients with liver and /or kidney dysfunction; 2. Patients who are allergic to the drugs used in the research; 3. Patients with previous chronic pain; 4. Patients with increased intracranial pressure or intraocular pressure; 5. Patients with preoperative sinus bradycardia or atrioventricular block; 6. Patients with schizophrenia, mania or any other mental illness; 7. Patients who lack the ability to consent and communicate; 8. Patients who recently take analgesic or sedative drugs.

Design outcomes

Primary

MeasureTime frame
Postoperative pain;The incidence of nausea and vomiting within 48 hours after operation;Plasma cortisol concentration;Plasma TNF-a concentration;Plasma IL-6 concentration;Median effective dose;

Secondary

MeasureTime frame
Time of extubation;The length of staying in the postanesthesia care unit;Length of anesthesia;Length of surgery;Length of postoperative hospital stay;Heart rate;Blood pressure;Pulse oxygen saturation; Time to wake up after anesthesia;

Countries

China

Contacts

Public ContactWang Weibing

Anqing Municipal Hospital

w2bwang@sina.com+86 135 0055 8021

Outcome results

None listed

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