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Investigating the Impact of Ice Application on the Venous Puncture Pain in the Pediatric Population

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record History

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  1. Notable Start date changed from estimate of Apr 10, 2024 to Jul 12, 2024v4 Show 5 more changesShow less
    • Trial status: Not Yet Recruiting to Active, Not Recruiting
    • Enrollment target: estimated 114 to confirmed 94
    • Primary completion date changed from estimate of Sep 30, 2024 to Nov 30, 2024
    • Study completion date: Nov 15, 2024 to Jun 7, 2026
    • Study description revised
  2. Notable Primary completion date: Jan 30, 2024 to Sep 30, 2024v3 Show 7 more changesShow less
    • Start date: Oct 10, 2023 to Apr 10, 2024
    • Enrollment target: 120 to 114
    • Study completion date: Mar 15, 2024 to Nov 15, 2024
    • Interventions: distraction technique (Other), ice application (Other) to control group (Other), ice application (Other)
    • Eligibility criteria revised
    • Study description shortened, about 12 words
    • Study title shortened, about 1 word
  3. Minor Primary completion date: Dec 30, 2023 to Jan 30, 2024
    • Study completion date: Feb 1, 2024 to Mar 15, 2024
    v2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
the goal of this RCT is: "To evaluate the effectiveness of a non-pharmacological method (ice application) in reducing venous puncture pain among children aged 5 to 7 years.". An (RCT) will be conducted, involving 94 children, a non-probability convenience sampling will be used and children will randomly assign to two groups by lottery method. One group will receive ice application as an intervention, while other group will be control group, having no ice application.
Trial Details
NCT Number NCT06089889
Lead Sponsor University of Health Sciences Lahore
Conditions
(from sponsor)
Venous Puncture Pain
Enrollment 94 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov