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Not Yet RecruitingNCT06397807

Postoperative Pain Management on Patients Undergoing Lung Tumor Resection

Postoperative Pain Management on Patients Undergoing Video-assisted Thoracoscopic (VATS) Lung Tumor Resection: a Prospective Cohort Study

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
400 (estimated)
Sponsor
China Medical University Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Multimodal analgesia (MMA) is an essential part of Enhanced Recovery After Surgery (ERAS) protocol. The principle of MMA is to manage pain with analgesics of multiple classes acting on distinct target sites through different strategies. MMA can reduce the adverse reaction caused by opioids and improve the quality of recovery from surgery. Inadequate postoperative pain management will increase the risk of complications, including pneumonia, deep vein thrombosis, infection, delayed surgical healing, and chronic postoperative pain.

Detailed description

This prospective, observational study is planned to investigate the efficacy of different MMA regimens conducting in our hospital. Patients undergoing video-assisted thoracoscopic (VATS) lung tumor resection will be invited to participate in the study and grouped based on the MMA regimens. Anxiety, quality of recovery, pain intensity will be evaluated pre- and post-operatively. Demographic data, surgery record, medicine record and postoperative complications will be gained from medical history system and analyzed.

Conditions

Interventions

TypeNameDescription
DRUGDinalbuphine sebacateDinalbuphine sebacate (DS) is a long-acting injectable. With oil-based formulation, DS will slowly releases to blood vessel and be hydrolyzed to nalbuphine after intramuscularly injection. The analgesic effect lasts around 5 to 7 days.
DRUGAnalgesic injectablesOpioids, NSAIDs or acetamol will be administrated as need.
DRUGEnteral analgesicsOpioids, NSAIDs or acetaminophen will be prescribed if necessary.

Timeline

Start date
2024-05-31
Primary completion
2026-03-02
Completion
2026-05-30
First posted
2024-05-03
Last updated
2024-05-03

Source: ClinicalTrials.gov record NCT06397807. Inclusion in this directory is not an endorsement.