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Wound clinical trials

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NCT ID: NCT03676556 Recruiting - Anesthesia, Local Clinical Trials

To Evaluate Reduction of Pain in Wounds Treatment Previously Applying Lidocaine Topical Solution vs Placebo.

Start date: June 16, 2021
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate if applying a lidocaine topical solution before wounds treatment decreases the pain of the procedure in comparison with placebo solution.

NCT ID: NCT03674749 Recruiting - Wound Clinical Trials

The Effects of Meditation and Hyperbaric Oxygen Therapy on Chronic Wounds

Start date: September 10, 2018
Phase: N/A
Study type: Interventional

In Ontario, wound care support has steadily increased over the years. With the growth of the aging population, the financial and psychological burden related to wound care will continue to rise. Studies have shown that structured meditation programs can improve on the recovery process for both physical and psychological disease. Therapeutic treatments like Hyperbaric Oxygen Therapy (HBOT) for chronic wounds have shown to promote angiogenesis, cerebral blood and neuroplasticity in patients with stroke, traumatic brain injury and chronic pain. By combining meditation and HBOT, this have been independently shown to improve healing and reducing costs associated with chronic wounds.

NCT ID: NCT03649308 Active, not recruiting - Wound Heal Clinical Trials

Negative Pressure Wound Therapy Compared to Traditional Care After Skin Grafting

TRUTH
Start date: September 19, 2018
Phase: N/A
Study type: Interventional

The aim of this study is to compare negative pressure wound therapy to traditional care after split-thickness skin grafting in patients aged over 18.

NCT ID: NCT03640871 Not yet recruiting - Wound Clinical Trials

HEAL Study: Healing Results, Efficacy and Acceptability of a New Contact Layer

HEAL
Start date: October 2018
Phase: N/A
Study type: Interventional

Assessment of efficacy, tolerance and acceptability for the wound dressing URGO AWC_019 in the treatment of acute wounds, chronic wounds and epidermolysis bullosa skin lesions

NCT ID: NCT03608384 Completed - Drug Use Clinical Trials

Characteristic of Drug Users Chronic Wound

TOXIPO
Start date: August 1, 2018
Phase:
Study type: Observational

The aim of this study is to describe demographic, clinical, etiological characteristic and evolution of drug addict's chronic wounds .

NCT ID: NCT03540004 Active, not recruiting - Wound Clinical Trials

Evaluation of MolecuLight i:X as an Adjunctive Fluorescence Imaging Tool to Clinical Signs and Symptoms for the Identification of Bacteria-containing Wounds

Start date: May 23, 2018
Phase:
Study type: Observational

This is a non-randomized evaluation for which 160 adult patients will be imaged at outpatient wound care clinics who present with a wound of unknown infection diagnostic status and are receiving standard treatment. The MolecuLight i:X Imaging Device will be used as an adjunctive tool in the assessment of the wound and may be used to guide the targeted sampling of a wound (using a conventional punch biopsy method).

NCT ID: NCT03512444 Completed - Wound Clinical Trials

Does Circumferential Negative Pressure Therapy Impair Distal O2 Saturation?

Start date: July 25, 2018
Phase: N/A
Study type: Interventional

Abstract: Background: Circumferential negative pressure wound therapy (CNPWT) is commonly used to manage wounds and enhance the healing process. A theoretical concern was recently raised that CNPWT may have a negative effect on perfusion distally. Objectives: We aim to evaluate the effect of circumferential negative pressure therapy (CNPT) on distal O2 saturation in healthy volunteers. Design: Randomized controlled non-inferiority study. Methods: Fourteen healthy adult volunteers with O2 saturation ≥95% (by index finger pulse oximetry) will be invited to participate in the study. After obtaining a written informed consent, CNPWT foam/dressing will be applied in a sandwich-like manner on the middle third of each arm and a negative intermittent pressure of 125 mmHg will be applied to one arm chosen randomly, using the contralateral arm as control. The pressure will be applied 5 minutes on and 2 minutes off for 9 hours. Individual's participation will be terminated if O2 saturation drops below 92% at any study time. The outcome measure is index finger O2 saturation and will be checked every 30 minutes using a pulse oximetry. The area under the curve (AUC) of O2 saturation in the 2 arms will be compared using ANCOVA. Sample size was calculated to have 90% power, assuming a type one error of 5%, non-inferiority margin of 24 (mean AUC difference), SD of 20, and drop out of 2 participants. Importance: The study is expected to provide conclusive evidence on the effect of intermittent CNPT on distal O2 saturation. The results would have direct implications for CNPWT.

NCT ID: NCT03396731 Completed - Venous Leg Ulcer Clinical Trials

Efficacy Study for Geko Device in VLU Patients

Start date: April 24, 2018
Phase: N/A
Study type: Interventional

Eight weeks, comprised of four weeks Run-in Phase of Standard Care (SC) treatment followed by four weeks of treatment allocated by randomisation (Treatment Phase). To compare two daily geko™ device treatment durations, six hours and 12 hours, in conjunction with SC, with each other and to SC alone, in patients with venous leg ulcers

NCT ID: NCT03386175 Recruiting - Wound Clinical Trials

Efficiency of Negative Pression Therapy With Instillation in the Debridement of Wound

TPN
Start date: October 4, 2017
Phase:
Study type: Observational

the aim of the study is to evaluate the efficiency of the therapy with negative pression (TPN) and instillation in the debridement of chronic wound

NCT ID: NCT03373513 Not yet recruiting - Pain Clinical Trials

Robotic-assisted Hysterectomy: Single- vs. Multi-port Laparoscopic Access

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

robotic single site surgery (R-SSH) is a novel technique, which may be superior to conventional multiport hysterectomy in select patients regarding cosmesis and postoperative pain. We, perform a randomized trial to compare R-SSH with multiport laparoscopic hysterectomy with regard to the postoperative rehabilitation, cosmesis, the operational cost, and the perioperative morbidity.