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A study on the prediction of postoperative chronic pain in Patients Undergoing thoracoscopic resection of Pulmonary Masses

A study on the prediction of postoperative chronic pain in Patients Undergoing thoracoscopic resection of Pulmonary Masses

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600116871
Enrollment
Unknown
Registered
2026-01-15
Start date
2026-01-15
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Chronic pain after thoracoscopic pulmonary mass resection in the patient

Interventions

choronic pain group:None
non-choronic pain group:None

Sponsors

The First Affiliated Hospital, Wenzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inpatients aged >=18 years who underwent PLT (posterolateral thoracotomy) or VATS (video-assisted thoracic surgery). Patients with normal mental status who are able to understand the Numeric Rating Scale (NRS). Informed consent was obtained, and patients with preoperative chronic pain, severe complications, or risk of loss to follow-up were excluded.

Exclusion criteria

Exclusion criteria: Patients with a history of chronic postoperative pain (which may be at a different site from the current surgery). Patients with critical preoperative conditions or those who are unable to cooperate. Patients who are unable to cooperate postoperatively due to severe complications or critical condition.

Design outcomes

Primary

MeasureTime frame
choronic postoperative pain;

Secondary

MeasureTime frame
Postoperative cognitive impairment;postoperative acute pain;

Countries

??

Contacts

Public ContactJiehao Sun

The First Affiliated Hospital, Wenzhou Medical University

sun_jiehao@126.com+86 136 7672 1930

Outcome results

None listed

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