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Effects of atomized Esketamine combined with dexmedetomidine on postoperative pharyngalgia and perioperative stress response in patients with colorectal cancer

Effects of atomized Esketamine combined with dexmedetomidine on postoperative pharyngalgia and perioperative stress response in patients with colorectal cancer

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072375
Enrollment
Unknown
Registered
2023-06-12
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

postoperative pharyngalgia

Interventions

Blank control group:Preoperative atomization of 5ml normal saline
Esketamine group:Preoperative atomization inhalation of 0.5mg/kg Esketamine plus normal saline to prepare 5ml
Dexmedetomidine group:Atomized inhalation of 1 ug/kg dexmedetomidine plus physiological saline is 5 ml
Dexmedetomidine combined with esketamine group:Atomized inhalation of 0.25mg/kg esketamine +0.5ug/kg dexmedetomidine plus normal saline was configured as 5ml 30min before surgery

Sponsors

Anesthesiology Research Institute, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, People’s Republic of China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ? ASA level I-II; ? Age = 18 years old; ? BMI<28kg/?? Laparoscopic colorectal cancer resection is planned to be performed on a selective basis; ? Preoperative evaluation predicts that there is no difficulty in intubation; ? Sign informed consent

Exclusion criteria

Exclusion criteria: ? History of sedative, hypnotic and analgesic abuse; ? Patients with uncontrolled hypertension, diabetes, severe stress, liver, kidney and other chronic diseases; ? History of chronic respiratory diseases (such as chronic obstructive pulmonary disease, chronic pharyngitis or asthma), recent history of respiratory infection; ? Preoperative VAS score>2 points; ? Preoperative evaluation predicts patients with intubation difficulties; ? Those who are allergic to general anesthetic ingredients; ? Patients who refused to participate in the study

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative sore throat;

Secondary

MeasureTime frame
heart rate;blood pressure;SpO2;VAS score;epinephrine;Norepinephrine;dopamine;

Countries

China

Contacts

Public ContactJianqing Lin

Anesthesiology Research Institute, The First Affiliated Hospital, Fujian Medical University, Fuzhou, 350005, People’s Republic of China

linjianqing72@fjmu.edu.cn+86 138 5014 3313

Outcome results

None listed

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