Clinical Trials Directory

Trials / Completed

CompletedNCT05061667

Thoracic Paravertebral Block Versus Rhomboid Block for Postoperative Pain Control in Thoracic Surgeries

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
88 (actual)
Sponsor
Koç University · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The main aim of this study is to compare thoracic paravertebral block and rhomboid block for postoperative analgesia and analgesic usage in thoracic surgeries.

Detailed description

Patients with scheduled thoracic surgery are going to be enrolled for this study. Patients will be randomized and separated in two groups. Group I will receive thoracic paravertebral block, group II will receive rhomboid block. Each group will receive patient controlled analgesia with intravenous fentanyl. Patients will be monitored at postoperative 1st, 3rd, 6th, 12th, 24th hours and their VAS scores, adverse reactions like nausea and vomiting, total analgesic usage, additional analgesic need and time of the first report of pain will be filed. Then the two groups will be compared and evaluated.

Conditions

Interventions

TypeNameDescription
PROCEDUREThoracic Paravertebral BlockParavertebral block for postoperative analgesia in thoracic surgery
PROCEDURERhomboid BlockRhomboid block for postoperative analgesia in thoracic surgery

Timeline

Start date
2021-01-01
Primary completion
2021-11-01
Completion
2021-12-15
First posted
2021-09-29
Last updated
2022-01-20

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT05061667. Inclusion in this directory is not an endorsement.