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Effect of esketamine combined with parecoxib sodium on postoperative analgesia and inflammatory response in patients with thoracoscopic pulmonary resection

Effect of esketamine combined with parecoxib sodium on postoperative analgesia and inflammatory response in patients with thoracoscopic pulmonary resection

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500095107
Enrollment
Unknown
Registered
2025-01-02
Start date
2025-01-05
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

lung tumor

Interventions

Esketamine group:Esketamine
Parecoxib sodium group:Parecoxib sodium
Esketamine combined with parecoxib sodium group:Esketamine combined with parecoxib sodium
control group:Normal saline

Sponsors

Yongchuan Hospital affiliated to Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. ASA grade grade I or II. 2. Age range between 50 and 80 years. 3. All patients met the indications for thoracic surgery, excluding patients with contraindications to general anesthesia, allergies to esketamine and parecoxib, and patients with previous chronic painful disease, chronic inflammatory disease.

Exclusion criteria

Exclusion criteria: 1. Allergic to the drug used. 2. A clear history of mental abnormalities and a long history of psychotropic medication, or a diagnosis of anxiety or depression. 3. Significant hepatic and renal insufficiency (blood transaminase and creatinine levels above the upper limit of normal). 4. Patients with a previous history of gastrointestinal bleeding. 5. Patients at serious risk of elevated intracranial pressure, such as intracranial aneurysms 6. Undercontrolled or untreated hypertension (resting systolic/ DBP over 180/ 100mmHg). 7. In a patient with hyperthyroidism (hyperthyroidism) without untreated or poor therapeutic efficacy. 8. Before surgery, the patient himself has serious complications, such as branch enlargement or tuberculosis.

Design outcomes

Primary

MeasureTime frame
Serum levels of IL-6 and CRP;

Secondary

MeasureTime frame
VAS score and dose and number of salvage medication;Changes in blood pressure and heart rate;Occurrence of adverse reactions;Development of complications;

Countries

China

Contacts

Public ContactYan Dong; Li Jingnan

Yongchuan Hospital affiliated to Chongqing Medical University

13983678546@163.com+86 139 8367 8546

Outcome results

None listed

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