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Correlation Analysis Between Different Levels of Preoperative Anxiety and Postoperative Pain in Thoracic Surgery Patients

Correlation Analysis Between Different Levels of Preoperative Anxiety and Postoperative Pain in Thoracic Surgery Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500115736
Enrollment
Unknown
Registered
2025-12-30
Start date
2026-02-28
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

posroperative pain

Interventions

Mild to moderate anxiety:None
High anxiety:None

Sponsors

Affliated hospital of Jining Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18 to 70 years. 2. Surgery type: Patients scheduled for elective thoracic surgery, including but not limited to lobectomy, segmentectomy, pneumonectomy, radical esophagectomy, etc. Surgical approaches may include thoracotomy and video-assisted thoracoscopic surgery (VATS). 3. ASA classification: American Society of Anesthesiologists (ASA) physical status I-III. 4. Cognitive and communication capacity: Patients must be conscious and able to understand and cooperate with the completion of all assessment scales. 5. Informed consent: Patients or their legally authorized representatives must voluntarily sign written informed consent to participate in the study and cooperate with follow-up.

Exclusion criteria

Exclusion criteria: 1. History of prior thoracic surgery: Patients who have previously undergone any form of thoracic surgery. 2. Severe comorbidities: ASA physical status >= IV, or severe functional insufficiency of vital organs (heart, brain, lung, liver, kidney, etc.) precluding surgical tolerance. 3. Psychiatric or neurological disorders: Diagnosed severe psychiatric illness (e.g., schizophrenia, major depression), cognitive dysfunction (e.g., dementia), or neurological disease preventing comprehension or completion of assessments. 4. Chronic pain history: Pre-existing chronic pain syndromes (e.g., fibromyalgia, neuropathic pain) with long-term analgesic use. 5. History of drug or alcohol abuse: Patients with a documented history of drug or alcohol dependence. 6. Refusal or inability to complete follow-up: Patients who refuse to sign informed consent, or are expected to be unable to complete follow-up during the study period for any reason.

Design outcomes

Primary

MeasureTime frame
Anxiety assessment;Pain assessment;

Secondary

MeasureTime frame
Surgical information: Duration of surgery, dosage of anesthetic drugs;Postoperative analgesic consumption;Postoperative adverse effects;

Countries

China

Contacts

Public ContactLi Xirong

Affliated hospital of Jining Medical University

619174227@qq.com+86 2903019

Outcome results

None listed

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