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Effect of low-dose esketamine on biliary-cardiac reflex and postoperative pain during laparoscopic cholecystectomy surgery: a randomized, controlled study

Effect of low-dose esketamine on biliary-cardiac reflex and postoperative pain during laparoscopic cholecystectomy surgery: a randomized, controlled study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079362
Enrollment
Unknown
Registered
2024-01-02
Start date
2024-01-15
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

cholecystectomy

Interventions

control group:Equal dose of normal saline was given before incision
esketamine group:0.3mg/kg esketamine was given before incision

Sponsors

Xiangyang Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) ASA grade ?-?; 2) Age =18 years old, weight 50-100kg, gender unlimited; 3) Patients undergoing cholecystectomy under general anesthesia; 4) Sign informed consent voluntarily.

Exclusion criteria

Exclusion criteria: 1) Known allergy to the active ingredients or excipients of esketamine hydrochloride injection; 2) suffering from severe cardiovascular and cerebrovascular diseases, respiratory diseases, blood diseases, endocrine diseases or liver and kidney dysfunction; 3) Increased risk of intraocular pressure (such as glaucoma), and intracranial pressure; 4) Combined with neurological or mental illness; 5) alcoholism or long-term use of sedatives and analgesics; 6) Patients who have undergone surgery or used experimental drugs within one week before surgery; 7) Participants who have participated in clinical trials of other drugs as subjects in the past 3 months; 8) Communication barriers (reading and writing Chinese barriers, language barriers, visual impairments or hearing impairments, etc.) can not cooperate with the completion of the research; 9) Those who refuse to sign informed consent.

Design outcomes

Primary

MeasureTime frame
biliary-cardiac reflex ;VAS pain score;

Secondary

MeasureTime frame
Intraoperative changes of blood pressure, heart rate and oxygen saturation;Postoperative opioid requirement;Preoperative and postoperative depression/anxiety (Hospital Anxiety and Depression Scale-HAD Scale) and cognitive function scores (Simple Intelligent Mental State Examination Scale (MMSE));

Countries

China

Contacts

Public ContactYexihong

Xiangyang Central Hospital

yezi903@126.com+86 137 9760 6442

Outcome results

None listed

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