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RecruitingNCT05282251

Intrapleural Nebulization of Bupivacain to Reduce Postoperative Pain

Pain Managment After VATS to Reduce Postoperative Pain and Improve Pulmonary Function

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Assiut University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Thoracic surgery is now common and as other surgeries evolution of minimally invasive techniques is employed. Video-assisted thoracic surgery (VATS) produces little scar but may produce severe pain that may affect the pulmonary function. Many procedure was developed like intercostal nerve block which require injections at multiple levels, Insertion of local anaesthetic (LA) in the surgical drain but that was dangerous due to the large amount of LA and not sufficient to completely eliminate pain. Bupvicaine nebulization, through surgical port which won't make any other wound, thought to be sufficient because Nebulization will enable us better distribution and less amounts of LA. Bupvicaine is local anaesthetic amide group that works by blocking sodium channels thus preventing progression of action potential.

Conditions

Interventions

TypeNameDescription
DRUGIntrapleural bupivacine nebulizationIntrapleural nebulization of bupivacine (10 ml of bupivacaine 0.5%) + Intravenous normal saline as a placebo
DRUGIntravenous paracetamol and ketorolacIntravenous analgesia: paracetamol (one gram) and Ketorolac (30 mg) + Intrapleural normal saline (10 ml) as a placebo

Timeline

Start date
2024-05-17
Primary completion
2024-07-15
Completion
2024-07-15
First posted
2022-03-16
Last updated
2024-05-20

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05282251. Inclusion in this directory is not an endorsement.

Intrapleural Nebulization of Bupivacain to Reduce Postoperative Pain (NCT05282251) · Clinical Trials Directory