Status:
COMPLETED
The Effect of Lidocaine and Benzocaine on Pain and Injection Satisfaction in Peripheral Intravenous Catheter Application
Lead Sponsor:
TC Erciyes University
Conditions:
Peripheral Intravenous Catheterization Application
Eligibility:
All Genders
18-65 years
Phase:
PHASE3
Brief Summary
Objective: This research was conducted as a randomized controlled, double-blind experimental study to determine the effect of topical lidocaine and benzocaine on patient's pain and injection satisfact...
Detailed Description
Objective: This research was conducted as a randomized controlled, double-blind experimental study to determine the effect of topical lidocaine and benzocaine on patient's pain and injection satisfact...
Eligibility Criteria
Inclusion
- Can speak and understand Turkish,
- Over the age of 18,
- Under the age of 65,
- Located in the green area of Erciyes University Emergency Service,
- Having orientation in place and time,
- Not using psychiatric medication due to any psychiatric illness,
- Not using central nervous system drugs,
- Does not have any known chronic disease,
- No vision or hearing problems,
- No signs of phlebitis, scar tissue, dermatitis, incision or infection in the area to be operated,
- Does not have pain anywhere on the body that will affect the result of the study and whose visual comparison scale pain score is zero at the time of application
- No experience of IV catheter application in the last month,
- Not taking analgesic in the last 24 hours,
- Intravenous drug treatment is ordered,
- With Baseline Algometer device, the average pressure pain threshold is 8-16 pounds (Lb),
- Individuals who volunteered to participate in the study and signed the written consent form were included in the study.
Exclusion
- Not wanting to participate in the study,
- A history of sensitivity to the study drug or related drugs or any drug excipient,
- Having clinically significant vital signs,
- Stating that he / she is addicted to alcohol and drugs,
- Those who were incompetent or unwilling to comply with the study protocol or who stated that they experienced difficulties in the procedures related to the study (eg establishing vascular access before) were not included in the study.
- In patients who developed IV catheter complications (swelling of the vascular access, hematoma) during the study,
- In patients whose IV catheter insertion cannot be performed at the first time,
- The study was terminated in patients who wanted to leave the study anywhere in the study.
Key Trial Info
Start Date :
March 4 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 20 2020
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT04859738
Start Date
March 4 2020
End Date
October 20 2020
Last Update
April 26 2021
Active Locations (1)
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1
Erciyes University
Kayseri, Turkey (Türkiye), 38039