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A randomized, controlled trial of esketamine in the perioperative period of thoracoscopic open reduction and fixation of rib fractures

A randomized, controlled trial of esketamine in the perioperative period of thoracoscopic open reduction and fixation of rib fractures

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040184
Enrollment
Unknown
Registered
2020-11-24
Start date
2020-12-01
Completion date
Unknown
Last updated
2021-11-22

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

Conditions

Rib fracture

Interventions

Esketamine group:Intraoperative and postoperative intravenous administration of Esketamine
Control group:Intraoperative and postoperative intravenous use of Physiological saline

Sponsors

Xiang'an Hospital of Xiamen University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 20-60 years; 2. American Association of Anesthesiologists (ASA) graded from I to III; 3. BMI between 18-26kg/m2; 4. Accepted general anesthesia and postoperative Analgesia; 5. Volunteer to participate and sign the informed consent form for clinical trials.

Exclusion criteria

Exclusion criteria: 1. Allergic to esketamine or general anesthesia drugs; 2. Poorly controlled grade 2 or above hypertension, glaucoma, hyperthyroidism, and intracranial hypertension; 3. Lung infections, chronic obstructive pulmonary disease and others that can cause hypoxemia; 4. Infections or inflammatory diseases; 5. Dependent on narcotic drugs.

Design outcomes

Primary

MeasureTime frame
Mean arterial pressure;Heart rate;Pulse oximetry;Respiratory rate;Type and dosage of analgesic drugs;VAS;Richmond Agitation-Sedation Scale;Wong-Baker Faces Pain Rating Scale;White blood cell count;C reactive protein;Tumor necrosis factor alpha;Interleukin-6;Interleukin-8;

Secondary

MeasureTime frame
Intraoperative airway pressure;Postoperative dizziness;Postoperative restlessness;Postoperative nausea and vomiting;Postoperative delirium;Frequency of analgesia pump use;

Countries

China

Contacts

Public ContactDeng Bin

Xiang'an Hospital of Xiamen University

xajxdb@126.com+86 18030224034

Outcome results

None listed

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