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Wound clinical trials

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NCT ID: NCT06464250 Completed - Diabetic Foot Ulcer Clinical Trials

The Effect of Bundle Approach on Foot Care Behaviors and Diabetic Wound Healing in Patients

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

This study was planned to standardize foot care behaviors with a patient-participated care package approach, to ensure healing of existing wounds, and to evaluate the effect on foot care behaviors to prevent the development of new diabetic foot ulcers. The sample of the study consisted of a total of 97 patients, 49 patients in the care package group and 48 patients in the control group. Hypotheses of the Study H1. The foot care behaviors of patients who receive a patient-participatory care package approach to diabetic foot ulcer prevention will be higher than those of patients who do not receive a care package. H2. Patient-involved care package approach prevents the development of new diabetic foot ulcers. H3. Patient-involved care package approach provides healing of existing diabetic ulcers.

NCT ID: NCT06388980 Active, not recruiting - Nurse's Role Clinical Trials

Knowledge and Needs of Nursing in Relation to the Treatment Complex Wounds

Start date: May 1, 2023
Phase:
Study type: Observational

Study with cross-sectional and descriptive mixed methodology. With questionnaires with likert-type questions (0-10) being the 10 with the highest score, and open questions in relation to knowledge in wound care; include all Corporaciló Sanitària Parc Taulí (CCSPT) nurses who voluntarily want to participate in a pseudo-anonymized surv

NCT ID: NCT06321978 Recruiting - Wound Clinical Trials

Mepilex Border Flex Utilization Pilot Spain

MxBFlexUPESP
Start date: February 16, 2024
Phase:
Study type: Observational

The aim of this study is to assess and describe the utilization of Mepilex® Border Flex and other foam dressings available in routine clinical practice in the management of patients with chronic wounds, in order to understand the pattern of use and the frequency of dressing changes in wound management. The study will also allow to gain information about the opinion of the HCPs and the patient's experience concerning wound management with foam dressings. This information may help to understand patient's health care optimization in terms of quality and efficiency.

NCT ID: NCT06309446 Completed - Wound Clinical Trials

Assessment of Wound Healing, Cooling Efficacy and Local Tolerability of a Wound Care Hydrogel

Start date: January 14, 2020
Phase: N/A
Study type: Interventional

Test the wound healing properties of the product as well as the cooling effect and tolerability of a wound care gel.

NCT ID: NCT06138964 Recruiting - Wound Heal Clinical Trials

Comparing the Effect of siSPARC Microneedle Patch Versus siSPARC+siLR4A Microneedle Patch on Post-surgical Scars

Start date: November 14, 2023
Phase: Phase 3
Study type: Interventional

This randomized, double-blind controlled study aims to compare the effect on appearance of post- surgical scars between daily application of siSPARC microneedle patch versus siSPARC + siLR4A microneedle patches. These patches comprising short microneedles embedded with hydrolysed RNA (siRNAs) have been classified by Health Science Authority, Singapore, as cosmetic products.

NCT ID: NCT06011421 Recruiting - Wound Clinical Trials

Wound Catheter Vs LA Bolus in Renal Transplant: RCT

Start date: January 31, 2022
Phase:
Study type: Observational

Pain control is an important part of patients' care after a kidney transplant. Currently patients receive a one off injection of Local Anaesthetic (LA) in the wound at the end of the operation followed by Intravenous morphine through a Patient Controlled Analgesia System (PCAS), a button pressed to provide a calculated dose with lock out times for safety. Through this study the aim to test the efficiency of Continuous Local Anaesthetic Infiltration via Wound Catheter (LAWC) which is a method to deliver Local Anaesthetic over a longer period of time after the operation. LAWC are currently in use in a variety of surgical specialities including Liver surgery. Patients participating in this study will be allocated randomly to one of 2 groups; one will receive LA at the end of the operation as per current practice and one will receive LAWC. It then compare outcomes such as the the dose of morphine required in the PCAS, quality of pain control and improvement in recovery.

NCT ID: NCT05930210 Recruiting - Diabetes Mellitus Clinical Trials

A Study to Evaluate ENERGI-F703 GEL in Diabetic Foot Ulcer

Start date: May 30, 2023
Phase: Phase 3
Study type: Interventional

This Phase 3 study is a randomized, double-blind, vehicle-controlled, multiple-center, parallel study to evaluate efficacy and safety of ENERGI-F703 GEL compared with vehicle control in subjects with Wagner Grade 1 to Grade 2 diabetic foot ulcers. Baseline target ulcer size (<16 cm2 vs ≥16 cm2 ) will be included as a stratification factor. Subjects will be randomized 1:1 to receive ENERGI-F703 GEL or vehicle control using an interactive web response system for randomization to automatically assign a unique subject randomization number. Total duration of the study will be up to 31 weeks including Screening visit (approximately 2 to 3 weeks), double-blind dosing/observation phase (16 weeks), and a safety follow-up of 12 weeks after the last administration of study treatment.

NCT ID: NCT05924867 Not yet recruiting - Wound Heal Clinical Trials

Plasma Activated Saline in Wound Treatment

Start date: July 20, 2023
Phase: N/A
Study type: Interventional

This is a prospective, open-label, randomized, parallel controlled clinical trial. The purpose of this study is to understand the application value of plasma-activated normal saline in the treatment of different types of wounds. The main questions it aims to answer are: 1. What is the effect of plasma activated normal saline in promoting wound healing of different types? 2. What is the safety of plasma activated normal saline in the treatment of wound surface? Subjects will be randomly divided into the intervention group and the control group. The intervention group will receive wound treatment with plasma activated normal saline, and the control group will receive routine dressing change treatment.

NCT ID: NCT05903547 Recruiting - Cesarean Section Clinical Trials

Skin Glue Cesarean Study

Start date: August 23, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to compare cesarean incision outcomes between patients with incision closed with the Dermabond Prineo system compared to standard subcuticular suture.

NCT ID: NCT05853237 Completed - Wound Heal Clinical Trials

Class iv Versus Class Iiib Laser Therapy on Median Sternotomy Healing After Coronary Artery Bybass Graft

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

LASER therapy is potent physiotherapy modalities, providing better sternotomy healing for patients who have undergone CABG surgery, compared with traditional wound care management alone. HLLT and LLLT were found to be the most effective methods for sternotomy healing post-CABG surgery, with HLLT offering superior performance in the case of the high deep penetration and significance less time needed to deliver the same joules/ cm compared to LLLT used for the wound site.