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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: 14 March 2016
Main ID:  NCT02296619
Date of registration: 13/11/2014
Prospective Registration: No
Primary sponsor: Tokat Gaziosmanpasa University
Public title: The Effects of Transversus Abdominis Plane Block in Patients Undergoing Total Abdominal Hysterectomy TAP
Scientific title: The Effects of TAP Block on Hemodynamic Variables, Anaesthetic and Analgesic Requirement and Quality of Recovery in Patients Undergoing Total Abdominal Hysterectomy
Date of first enrolment: September 2014
Target sample size: 66
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02296619
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Supportive Care  
Phase:  Phase 4
Countries of recruitment
Turkey
Contacts
Name:     Tugba Karaman, MD
Address: 
Telephone:
Email:
Affiliation:  GOU
Key inclusion & exclusion criteria

Inclusion Criteria:

- Adult (18-65years old)

- American Society of Anesthesiologists (ASA) physical status I-II

- Patients scheduled for elective total abdominal hysterectomy under general anesthesia

Exclusion Criteria:

- ASA physical status = 3

- Allergy to local anesthetics

- Drug abuse or addiction

- Bleeding tendency



Age minimum: 18 Years
Age maximum: 65 Years
Gender: Female
Health Condition(s) or Problem(s) studied
Intraoperative Complications
Abdominal Hysterectomy (& Wertheim)
Intervention(s)
Procedure: Control
Procedure: TAP block
Primary Outcome(s)
intraoperative opioid consumption [Time Frame: during anaesthesia]
Secondary Outcome(s)
intraoperative hemodynamic variables [Time Frame: during anaesthesia]
Postoperative nausea and vomiting [Time Frame: postoperative 0.,2.,12.,24 hours]
Quality of recovery [Time Frame: postoperative 24 hours]
intraoperative anaesthetic consumption [Time Frame: during anaesthesia]
postoperative pain [Time Frame: postoperative 0,2,12,24 hours]
Secondary ID(s)
GaziosmanpashaU
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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