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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 23 February 2016
Main ID:  NCT02671851
Date of registration: 22/01/2016
Prospective Registration: No
Primary sponsor: Istanbul University
Public title: Ultrasound-Guided Thoracic Paravertebral Blocks in Patients Undergoing Reduction Mammoplasty
Scientific title: Ultrasound-Guided Bilateral Thoracic Paravertebral Blocks as an Adjunct to General Anaesthesia in Patients Undergoing Reduction Mammoplasty: A Historical Cohort Study
Date of first enrolment: January 2014
Target sample size: 64
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02671851
Study type:  Observational
Study design:  Observational Model: Cohort, Time Perspective: Retrospective  
Phase:  N/A
Countries of recruitment
Turkey
Contacts
Name:     Emine A Salviz, MD
Address: 
Telephone:
Email:
Affiliation:  Design and conduct the study, review and analyze the data, and write the manuscript
Key inclusion & exclusion criteria

Inclusion Criteria:

- ASA I-III patients who underwent bilateral reduction mammoplasty

Exclusion Criteria:

- Patients with deficient data



Age minimum: 18 Years
Age maximum: 70 Years
Gender: Female
Health Condition(s) or Problem(s) studied
Pain, Postoperative
Intervention(s)
Drug: Thoracic paravertebral blocks (TPVBs)
Drug: IV metamizole sodium, paracetamol
Primary Outcome(s)
Time to first pain [Time Frame: 0-48 hours]
Secondary Outcome(s)
Rescue analgesic requirement [Time Frame: 0-48 hours]
Surgeon satisfaction (Satisfaction scores) [Time Frame: 0-48 hours]
Pain (NRS) scores [Time Frame: 0-48 hours]
Tramadol use [Time Frame: 0-2 hours]
Fentanyl use [Time Frame: During the surgery]
Patient satisfaction (Satisfaction scores) [Time Frame: 0-48 hours]
Incidence of Postoperative nausea and vomiting (PONV) [Time Frame: 0-48 hours]
Length of stay in the PACU [Time Frame: 0-2 hours]
Secondary ID(s)
2016/83
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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