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The Effect of Obesity on Venous Puncture Pain

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03689205
Recruitment Status : Unknown
Verified September 2018 by Hakan Tapar, Tokat Gaziosmanpasa University.
Recruitment status was:  Recruiting
First Posted : September 28, 2018
Last Update Posted : September 28, 2018
Sponsor:
Information provided by (Responsible Party):
Hakan Tapar, Tokat Gaziosmanpasa University

Study Description
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Brief Summary:
Before surgery, patients will fill the Beck anxiety, distress tolerance test and Pain katastrophizing test. Patients will be divided into two groups according to BMI> 30kg / m2 (Group A) and BMI <30kg / m2 (Group B). Compared to body weight, venous vascular pain of the groups will be compared.

Condition or disease
Pain Cannulation Body Mass Index

Detailed Description:
Seventy patients will be randomized to two groups(BMI> 30kg / m2 (Group A) and BMI <30kg / m2 (Group B) during peripheral venous cannulation (PVC). The patients' visual analog scores will be measured during peripheral venous cannulation.
Study Design
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Study Type : Observational
Estimated Enrollment : 70 participants
Observational Model: Other
Time Perspective: Prospective
Official Title: Assessment of the Effect of Obesity on Venous Puncture Pain
Actual Study Start Date : June 20, 2018
Estimated Primary Completion Date : October 20, 2018
Estimated Study Completion Date : November 20, 2018
Groups and Cohorts
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Group/Cohort
Patients that BMI> 30kg / m2 (Group A)
Venous puncture pain on patients that Body mass index > 30kg / m2
Patients that BMI< 30kg / m2 (Group B)
Venous puncture pain on patients that Body mass index < 30kg / m2


Outcome Measures
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Primary Outcome Measures :
  1. Visual analog scale [ Time Frame: one month ]
    pain intensity


Eligibility Criteria
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Ages Eligible for Study:   18 Years to 65 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
After surgery patients
Criteria

Inclusion Criteria:

  • American Society of Anesthesiologist (ASA) physical status 1 and 2, between the ages of 18 and 65, were scheduled for elective surgery

Exclusion Criteria:

  • Patients with a history of anxiety disorders or hearing problem and preoperative pain, emergency surgery
Contacts and Locations
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Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03689205


Contacts
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Contact: Hakan Tapar 03562129500 ext 3497 hakantapar@hotmail.com
Contact: Hakan Tapar 03562129500 ext 3497 akantapar@hotmail.com

Locations
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Turkey
Gaziosmanpasa University Recruiting
Tokat, Turkey, 60200
Contact: Hakan Tapar, Assist.Prof.    +905056844496    hakantapar@hotmail.com   
Sponsors and Collaborators
Tokat Gaziosmanpasa University
Investigators
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Principal Investigator: Hakan Tapar Gaziosmanpasa University
More Information
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Responsible Party: Hakan Tapar, Assist. Prof, Tokat Gaziosmanpasa University
ClinicalTrials.gov Identifier: NCT03689205    
Other Study ID Numbers: 18-KAEK-101
First Posted: September 28, 2018    Key Record Dates
Last Update Posted: September 28, 2018
Last Verified: September 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Obesity
Overnutrition
Nutrition Disorders
Overweight
Body Weight