Completed
Single Injection, Ultrasound Guided Paravertebral Block for Anesthesia in Breast Surgery.
What is being collected
Data Collection
Collected from today forward - ProspectiveWho is being recruted
Breast Diseases+3
+ Neoplasms
+ Neoplasms by Site
From 18 to 90 Years
+5 Eligibility Criteria
How is the trial designed
Observational
Study Start: November 2011
Summary
Principal SponsorCampus Bio-Medico University
Last updated: March 27, 2013
Sourced from a government-validated database.Claim as a partner
Study start date: November 1, 2011
Actual date on which the first participant was enrolled.General anaesthesia is currently the conventional technique used for breast surgery. Thoracic Paravertebral block (PVB) has been used with multiple injection. We compared a single injection thoracic PVB with general anaesthesia (GA) in 20 consenting patients, scheduled for unilateral breast surgery.
Principal SponsorCampus Bio-Medico University
Last updated: March 27, 2013
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
20 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Conditions
Criteria
Female
Biological sex of participants that are eligible to enroll.From 18 to 90 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Breast DiseasesNeoplasmsNeoplasms by SiteSkin DiseasesSkin and Connective Tissue DiseasesBreast Neoplasms
Criteria
3 inclusion criteria required to participate
Age older than 18 years old
American Society of Anesthesiologists classification I-III
Written informed consent
2 exclusion criteria prevent from participating
allergy to local anesthetics
local sepsis
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Treatment Groups
Study Objectives
2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
CompletedOne Study Center