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Wound Heal clinical trials

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NCT ID: NCT05252260 Completed - Wound Heal Clinical Trials

Comparison of Diode Laser-Assisted Vestibuloplasty And Conventional Vestibuloplasty

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

Randomized controlled parallel designed clinical study aimed to compare vestibule depth gain and dimensional changes of wound area in individuals who underwent vestibule deepening surgery using diode laser and conventional technique

NCT ID: NCT05186532 Completed - Pain, Postoperative Clinical Trials

Dry Heat Versus Sitz Bath On Episiotomy Wound Heating And Pelvic Pain

Dry_Heat
Start date: January 5, 2021
Phase: N/A
Study type: Interventional

Objective: To compare the effect of dry heat versus moist heat application on episiotomy wound healing and pain among postnatal mothers. Research hypothesis H0: Postnatal mothers who apply dry heat on their episiotomy wound experience the same wound healing and pain as those who apply moist heat. H1: Postnatal mothers who apply dry heat on their episiotomy wound experience faster wound healing and less pain than those who apply moist heat. H2: Postnatal mothers who apply moist heat on their episiotomy wound experience faster wound healing and less pain than those who apply dry heat.

NCT ID: NCT05023135 Completed - Burns Clinical Trials

DeepView SnapShot Portable (DV-SSP): Device Training Study

Start date: September 7, 2021
Phase:
Study type: Observational

The purpose of this study is to continue development and validation of an algorithm for burn healing assessment by the Spectral MD DeepView device and provide burn healing potential assessment.

NCT ID: NCT04898816 Completed - Wound Heal Clinical Trials

Comparing the Effectiveness of Cyanoacrylate Tissue Adhesives and Conventional Sutures

Start date: March 30, 2020
Phase: N/A
Study type: Interventional

This study compares the effectiveness of two materials used for intraoral wound closure after removal of impacted mandibular third molar tooth. One Group received braided black silk suture and the other group received N-butyl 2-octyl cyanoacrylate tissue adhesives.

NCT ID: NCT04865952 Completed - Wound Heal Clinical Trials

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

Start date: April 29, 2021
Phase: N/A
Study type: Interventional

The purpose of the present study is to evaluate the effect of Hyaluronic acid application in the gene expression profile and cellular behavior in the early wound healing process -24 hours after injury- of the oral soft tissues.

NCT ID: NCT04834817 Completed - Wound Heal Clinical Trials

Effect of Combined Red and Near Infrared Light-emitting Diode (LED) Therapy on Tissue Regeneration Post Laser Treatment

Start date: April 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of light therapy on wound healing after laser treatment.

NCT ID: NCT04805463 Completed - Wound Heal Clinical Trials

Different Platelet Concentrates After Gingivectomy and Gingivoplasty Evaluation of Its Effect on Early Wound Healing.

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

The aim of this study was to evaluate the effect of PRF, CGF and AFG application on early wound healing after gingivectomy and gingivoplasty operations. In the study designed split mouth, gingivectomy and gingivoplasty surgery were performed on 19 patients. The postoperative PRF, CGF, and AFG applied areas were compared with the control regions. 0th,7 th,14 th and 28 th on the days, the surgical area was painted with mira-2-tone solution and evaluated in the ImageJ program. Measurements of clinical periodontal parameters including PI, GI, SC and SD were recorded at the beginning, after IPT and 28 days after the operation. Wound healing was evaluated with H2O2 test, VAS-Pain, and LTH index on 7th, 14th and 28th days. The patients were asked to evaluate their aesthetic perceptions on the VAS aesthetic scale.

NCT ID: NCT04794621 Completed - Wound Heal Clinical Trials

Electroceutical Dressing Technology (EDT) Against Wound Microbial Biofilm Infection

EDT BioFilm
Start date: June 3, 2021
Phase: N/A
Study type: Interventional

There are currently limited treatments available that show anti-biofilm efficacy for wound infection management Biofilms account for over 80% of infections and approximately 65% of nosocomial infections caused by microorganisms in the developed world involve biofilms. There clearly is a need for cost effective, highly stable, easily obtained biofilm targeted strategies for treatment of chronic wound biofilm infections. The information generated from this project has the potential of providing considerable benefits to wound care by determining the efficacy of EDT dressing in managing wound biofilm infection and efficacy in wound healing and closure. Such knowledge could help therapeutic strategies and could provide information for future clinical studies to further understanding -of EDT wound dressings.

NCT ID: NCT04697082 Completed - Pain Clinical Trials

Application of Platelet-rich Plasma in Pilonidal Sinus Disease

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

Pilonidal sinus disease is a common health-care problem, and surgical excision is the standard treatment modality. Controversy still exists regarding the best surgical technique for treating pilonidal disease in terms of minimizing disease recurrence and patient discomfort. In this study, the investigators compared the impact of autologous platelet-rich plasma (PRP) with that of minimally invasive techniques on pain reduction, return to daily activities, quality of life, and duration of wound healing after open excision and secondary closure.

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).