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Clinical application of esketamine in postoperative intravenous analgesia of chest patients

Clinical application of esketamine in postoperative intravenous analgesia of chest patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100054418
Enrollment
Unknown
Registered
2021-12-17
Start date
2021-12-15
Completion date
Unknown
Last updated
2022-11-20

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

Conditions

thoracoscopic lung surgery

Interventions

Experimental Group:PCIA uses esketamine

Sponsors

Gansu Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Thoracic patients undergoing thoracoscopic lung surgery; 2. Aged 18 to 65 years; 3. ASA classification I ~ II; 4. BMI18-30; 5. Clear consciousness, basic reading comprehension ability, normal vision and hearing; 6. No history of mental illness or cognitive dysfunction in the past, and can express their feelings in language; 7. Voluntarily participate in this study, understand and sign the informed consent form, and cooperate with those who complete the intervention and assessment.

Exclusion criteria

Exclusion criteria: 1. Those who are allergic to or have contraindications to the use of drugs and excipients during surgery and postoperative analgesia; 2. Participate in other clinical studies within 3 months before being enrolled in this study; 3. Those with dysfunction of important organs such as the heart, liver and kidney; 4. Being pregnant.

Design outcomes

Primary

MeasureTime frame
SF-MPQ questionnaire score;PHQ-9 questionnaire score;pain score;

Secondary

MeasureTime frame
recovery quality;rescue analgesia;adverse reactions;

Countries

China

Contacts

Public ContactYan Wenjun

Gansu Provincial Hospital

gsywj2008@hotmail.com+86 13893370700

Outcome results

None listed

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