Clinical Trials Directory

Trials / Completed

CompletedNCT04241640

Nefopam for Post Video-Assisted Thoracoscopic Lobectomy

Nefopam for Post Video-Assisted Thoracoscopic Lobectomy Pain Management and the Improvement of Enhanced Recovery After Surgery (ERAS): a Randomized Controlled Trial

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
72 (actual)
Sponsor
Mahidol University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Accepted

Summary

Video-assisted thoracoscopic (VATs) lobectomy is mild to moderately pain procedure. For conventional thoracotomy, there are many invasive pain control such as epidural analgesia, paravertebral block. However, for VATs, the invasive pain control somehow are too invasive. Nefopam is non-opioid painkilling medication, Serotonin, norepinephrine, dopamine reuptake inhibitor. Many study were demonstrated positive outcome of nefopam usage in many operation such as abdominal surgery, laparocopic surgery, orthopedic surgery. Nevertheless, nefopam for VATs is not well studied yet.

Conditions

Interventions

TypeNameDescription
DRUGNefopam 20 MG/MLNefopam group nefopam 20 mg during surgery and follow by 80 mg in 24 hours postoperative
DRUGPlaceboPlacebo

Timeline

Start date
2020-09-01
Primary completion
2022-08-01
Completion
2023-03-01
First posted
2020-01-27
Last updated
2024-11-20

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT04241640. Inclusion in this directory is not an endorsement.