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Venipuncture clinical trials

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NCT ID: NCT03899766 Completed - Venipuncture Clinical Trials

Support Activities for the Reduction of Distress and Pain in Children During Venipuncture

Start date: February 12, 2016
Phase:
Study type: Observational

To evaluate the efficacy of Health Support Activities (Animal Assisted Intervention, Clows, Musicians) in the reduction of pain and distress in children undergoing venipuncture. Hypothesis: the investigators expect a reduction in in pain and distress.

NCT ID: NCT03139045 Completed - Geriatric Clinical Trials

Impact of VeinViewer® Vision to Guide Peripheral Venipuncture in Geriatrics

VeinGER
Start date: September 1, 2018
Phase: Phase 3
Study type: Interventional

Peripheral venipuncture is a common procedure in geriatrics. This procedure due to altered cutaneous alteration and venous capital associated with age poses problems of comfort and quality of life of elderly patients hospitalized. There is little data from the literature that highlights the difficulties of venipuncture in the context of old age. New venous visualization technologies by infrared spectroscopy (NIR) such as VeinViewer® Vision (VVV) have been developed to guide the placement of a peripheral venous (VVP) or venipuncture (PV) route.

NCT ID: NCT03122574 Completed - Venipuncture Clinical Trials

The Effects of Aromatherapy on the Incidence and Severity of Acute Pain

Start date: November 2015
Phase: N/A
Study type: Interventional

The purpose of this research was to estimate feasibility of an aromatherapy pain management intervention to reduce pain and distress caused by venipunctures in a pediatric population. The feasibility of the use of aromatherapy essential oil lavandula angustifolia for pain management intervention (Treatment Group) was compared to placebo aromatherapy with jojoba oil (Placebo Control Group) and to the current standard of care, which is no oil during a venipuncture (Standard of Care Control Group). Primary measured outcomes were assessed using a double-blind randomized design. The physiological measure of heart rate was taken over the course of four minutes at three different intervals to note the pattern of change that occurs during anticipatory anxiety resulting from the impending procedure, the procedural pain experienced during the venipuncture, and the residual fear common after completion of the venipuncture procedure. The Visual Analogue Scale (VAS) for pain and the Hospital Fears Rating Scale (HFRS) were administered to measure subjective pain and anxiety. Participants (N=21) were recruited from the Laboratory Medicine Unit of Children's National Health System. Feasibility was estimated based on the ability to inhale the full dose of oil without adverse effects and and ability to inhale the full dose within the ten-minute time frame. This study analyzed the effect of the aromatherapy pain management intervention, lavandula angustifolia aromatherapy, on the stress response of a pediatric population through observation of physiological and psychological indicators of pain and distress, in order to learn more about the pain and anxiety experienced during venipuncture and the use of aromatherapy to decrease pain and anxiety during venipuncture.

NCT ID: NCT03004456 Completed - Pain, Procedural Clinical Trials

Distraction for Reduction of Pain Associated With Venipuncture in the Pediatric Post-Transplant Population

Start date: May 10, 2017
Phase: N/A
Study type: Interventional

Children with chronic diseases, particularly those who have received transplantation (e.g. cardiac, renal, or liver) are a population who undergo frequent painful procedures, such as venipuncture multiple times per week. There is currently no standard of care for pain reduction during venipuncture for pediatric patients having blood drawn in phlebotomy as an outpatient. The study aims to determine the efficacy of distraction in reducing procedural pain and distress associated with venipuncture in pediatric post-transplant patients.

NCT ID: NCT01115062 Completed - Pain Clinical Trials

Comparison of Synera Patch Versus LMX-4 Cream Versus Placebo Patch for Pain Reduction During Venipuncture in Children

Start date: April 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the effect of Synera patch versus LMX-4 cream and placebo on the level of pain, observed distress, difficulty of venipuncture and skin side effects in children undergoing intravenous blood draw in the emergency setting or the phlebotomy lab.

NCT ID: NCT00233844 Completed - Pain Clinical Trials

Studying the Analgesic Mechanism of the "Cough-Trick"

Start date: February 2004
Phase: Phase 2
Study type: Interventional

The aim of the trial is to study the possible mechanism of the pain reducing effect of CT at peripheral venipuncture