Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06947525

Effects of Shotblocker and Manual Pressure on Pain and Satisfaction

Effects of Shotblocker and Manual Pressure on Pain and Satisfaction During Peripheral Venous Catheter Placement: A Randomized Controlled Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
81 (estimated)
Sponsor
Necmettin Erbakan University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This study aims to determine the effects of shotblocker and manual pressure applied during peripheral venous catheter placement on pain and satisfaction. 81 patients hospitalized in the Urology clinic will be included in the study. Patients will be assigned to three groups as shotblocker (n=27), manual pressure (n=27) and control group (n=27) by block randomization method. Research Hypotheses * H1-1: The mean pain scores of the intervention group to which shotblocker was applied during peripheral intravenous catheterization are different from the control group. * H1-2: The mean pain scores of the intervention group to which manual pressure was applied during peripheral intravenous catheterization are different from the control group. * H1-3: The mean satisfaction scores of the intervention group to which shotblocker was applied during peripheral intravenous catheterization are different from the control group. * H1-4: The mean satisfaction scores of the intervention group to which manual pressure was applied during peripheral intravenous catheterization are different from the control group.

Conditions

Interventions

TypeNameDescription
OTHERManual pressureBefore the procedure in the manual pressure group, the vein entry area will be pressed with the right hand thumb for 10 seconds. The pressure will be applied until the nail bed turns white.
OTHERShotblockerIn the Shotblocker group, the shotblocker will be placed 2 cm above the vein entry point and will remain throughout the procedure.

Timeline

Start date
2025-04-28
Primary completion
2025-04-28
Completion
2025-06-30
First posted
2025-04-27
Last updated
2025-04-27

Source: ClinicalTrials.gov record NCT06947525. Inclusion in this directory is not an endorsement.