Skip to content

A trial of the effects of chronic pain related factors and postoperative analgesic effect during perioperative period in Department of thoracic surgery

A trial of the effects of chronic pain related factors and postoperative analgesic effect during perioperative period in Department of thoracic surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016379
Enrollment
Unknown
Registered
2018-05-28
Start date
2018-06-01
Completion date
Unknown
Last updated
2018-06-05

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

Conditions

lung cancer

Interventions

A:PCIA+ Flurbiprofen Axetil Injection + buprenorphine transdermal patch
B:PCIA+ Flurbiprofen Axetil Injection
C:Flurbiprofen Axetil Injection + buprenorphine transdermal patch

Sponsors

Affiliated Hospital of Qingdao University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) voluntarily participate in the study and sign informed consent by myself or his legal representative (if necessary); 2) Aged 18-75 years male and female; 3) operation mode lobectomy (single leaf or lobar) excision + systematic lymphadenectomy; 4) preoperative staging was excluded from late stage and distant metastasis; 5) to understand the use of visual analogue pain score (VAS) and intravenous patient controlled analgesia (PCIA); 6) non pregnancy patients.

Exclusion criteria

Exclusion criteria: 1) anticancer therapy such as radiotherapy and chemotherapy before operation; 2) the mode of operation was cuneiform resection / pneumonectomy. 3) patients with serious cardiovascular or cerebrovascular diseases or incomplete medical records. 4) patients who did not sign the informed consent form; 5) preoperative application of pain medication or serious postoperative complications; 6) patients with postoperative bleeding or persistent pulmonary leakage need re-operation; 7) patients who are participating in other clinical trials; 8) the researchers believe that other reasons are not suitable for clinical trials.

Design outcomes

Primary

MeasureTime frame
The best solution for postoperative analgesia in Department of thoracic surgery;

Countries

China

Contacts

Public ContactYongjie Wang

Affiliated Hospital of Qiingdao University

wangyongjie317@163.com+86 15615886677

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 28, 2026