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Wound Heal clinical trials

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NCT ID: NCT04669626 Completed - Wound Heal Clinical Trials

The Ability of Octenilin® to Reduce Odour of Malodorous Wound

Odour
Start date: July 1, 2020
Phase: N/A
Study type: Interventional

Malodours are a common complication of chronic wounds. They are the result of the proliferation of aerobic and anaerobic micro-organisms on the wound surface, where they metabolize healthy tissue which leads to the production of sloughy and even necrotic tissue. Wound odour has a big impact on the quality of life of patients. Currently the standard of care for the management of malodourous wounds are systemic antibiotics, absorbent wound dressings with or without activated carbon and, topical antimicrobials. The application of topical antimicrobials such as antiseptics against wound odour is part of the standard care. One suggested antiseptic in a recent published standard is Octenilin®. There is ample anecdotal evidence about the efficacy of Octenilin® in reducing wound odour. Therefore, we propose here to document this ability by evaluating the odour of wounds washed with Octenilin® versus standard care (NaCl 0.9% solution).

NCT ID: NCT04545476 Completed - Wound Heal Clinical Trials

Enhanced Secondary Intention Healing vs. Standard Secondary Intention Healing in Mohs Surgical Defects on the Head and Distal Lower Extremities

Start date: October 8, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to elucidate if a novel biomaterial containing gelatin, manuka honey, and hydroxyapatite enhances secondary intention healing when compared to conventional secondary intention healing for surgical defects after Mohs micrographic surgery on the head and distal lower extremities (below the knee). This novel biomaterial has already been FDA cleared for surgical wounds.

NCT ID: NCT04542486 Completed - Pain, Postoperative Clinical Trials

Clinical Efficacy of Soft Tissue Trimmer in Cases of Gingival Hyperplasia.

Start date: January 28, 2021
Phase: N/A
Study type: Interventional

Postoperative pain and wound healing are compared after using conventional scalpel technique in comparison with the intervention which is using Soft tissue Trimmer for cases of gingival hyperplasia.

NCT ID: NCT04514783 Completed - Wound Heal Clinical Trials

Healthy Tissue Preservation During Wound Debridement by Using Debritom+ Micro Water Jet Technology

Debritom
Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Chronic wounds are common and carry out an important and often neglected burden not only to the individual, the family but also to the society as a whole. The therapeutic approach to the management of chronic wounds include wound bed preparation or wound dressing management. Wound bed preparation is a concept emphasizing a holistic and systematic approach to evaluate and remove barriers to the healing process to allow the wound healing process to progress normally. Debridement is an integrated part of wound bed preparation, achieving certain goals and, thus, creating a healthy wound bed, margins and peri-wound skin with the objective to promote and accelerate healing. Debridement is defined as the removal of foreign material and necrotic tissue from a wound and it can also help to stimulate wound healing. However, not all methods of debridement are the same. Each method has advantages and disadvantages that must be clearly understood. In the present clinical practice, there are several methods of wound debridement: autolytic, enzymatic, mechanical, surgical (sharp) and biologic. The most common method is the mechanical debridement. Currently a micro-water jet technique was introduced into clinical practice. The micro-water jet technique Debritom+ is an effective alternative to traditional instrument interventions performed with the scalpel and/or curette. A sterile liquid is expelled from a nozzle at a selected intensity and accurately sprayed onto the wound surface. The desired effect is the generation of targeted micro-bleedings to stimulate regeneration and healing processes while preserving the underlying healthy tissue. Today, there is no clinical evidence quantitatively comparing one debridement method over the other. Therefore the invesitgators propose a pilot study to measure the extent of tissue loss after debridement using Debritom+ micro-water jet technology versus traditional instrument debridement procedure using scalpel and curette.

NCT ID: NCT04473859 Completed - Wound Heal Clinical Trials

Study to Evaluate the Safety of FSR Peptide Versus Placebo Following Punch Biopsy

Start date: March 6, 2008
Phase: Phase 1
Study type: Interventional

The purposes of this study is to test the safety of the study drug (FSR peptide) after a punch biopsy in healthy subjects.

NCT ID: NCT04417647 Completed - Wound Heal Clinical Trials

G-Wound (VZ for Wound Treatment)

Start date: June 5, 2020
Phase: N/A
Study type: Interventional

This is a prospective, randomized, open-label, controlled, exploratory trial that aims to investigate the local skin tolerability of topically administered VZ and to evaluate efficacy and safety parameters associated with improved wound condition and healing

NCT ID: NCT04391257 Completed - Stroke Clinical Trials

Study of gekoTM Interaction With Cardiac Pacemakers

Start date: December 4, 2020
Phase: N/A
Study type: Interventional

The gekoTM device is a small disposable battery powered device that attaches to the lower leg near the knee and stimulates the common peroneal nerve, causing muscle contraction of the lower leg. This contraction increases blood flow and the device is used to treat several conditions including deep vein thrombosis and venous leg ulcers. There is evidence that some powered muscle stimulators and related devices can affect Cardiac Demand Pacemakers. This study is to ascertain if there is any such interaction between the gekoTM device and permanently implanted cardiac pacemakers.

NCT ID: NCT04334421 Completed - Rectal Cancer Clinical Trials

APEMESH- Preventing Perineal Complications After Abdominoperineal Resection

Start date: April 3, 2020
Phase:
Study type: Observational

Abdominoperineal resection leaves an empty space to be filled by mesh or musculocutaneus flap. Several studies have reported over 30% morbidity with perineal wound healing after abdominoperineal resection. Preoperative radiotherapy is a strong predictor for perineal complications. Musculocutaneus flaps and use of biological mesh seem to minimize perineal morbidity. The role of omentoplasty at APR is controversial. Previous studies on synthetic mesh repair on perineum are almost lacking.

NCT ID: NCT04276129 Completed - Wound Heal Clinical Trials

Early Healing of Oral Soft Tissues: a Clinical and Biomolecular Analysis. Part II

Start date: February 20, 2020
Phase: N/A
Study type: Interventional

The purpose of the present study is to evaluate the influence of the post-surgical chlorhexidine indication in the gene expression profile and cellular behavior in the early wound healing process -24 hours after injury- of the oral soft tissues. The main hypothesis is that the post-surgical use of chlorhexidine affects the gene expression and the celular behavior in the early wound healing process of the soft oral tissues.

NCT ID: NCT04223089 Completed - Wound Heal Clinical Trials

Accuracy of TCOM vs NIRS in Predicting Wound Outcomes in Patients Treated With or Without Revascularization

Start date: December 17, 2019
Phase:
Study type: Observational

The primary purpose of this project is to compare the accuracy of transcutaneous oxygen monitoring and near infrared spectroscopy in assessing cutaneous oxygen levels in chronic wounds of patients following revascularization procedures as well as those with conservatively managed chronic wounds. This study will also compare the efficiency and practicality of both methods in guiding treatment decisions and management of these wounds.