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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03689205
Other study ID # 18-KAEK-101
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 20, 2018
Est. completion date November 20, 2018

Study information

Verified date September 2018
Source Tokat Gaziosmanpasa University
Contact Hakan Tapar
Phone 03562129500
Email hakantapar@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date November 20, 2018
Est. primary completion date October 20, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Turkey Gaziosmanpasa University Tokat

Sponsors (1)

Lead Sponsor Collaborator
Tokat Gaziosmanpasa University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual analog scale pain intensity one month
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