Clinical Trials Logo

Wound Heal clinical trials

View clinical trials related to Wound Heal.

Filter by:

NCT ID: NCT03819244 Completed - Postoperative Pain Clinical Trials

Comparison of Er,Cr:YSGG and Diode Lasers In Second Stage Implant Surgery

Start date: November 27, 2017
Phase: N/A
Study type: Interventional

The study evaluates postoperative pain, intraoperative bleeding and wound healing after second stage implant surgery. Submerged implants were exposed with diode laser in Group 1 (n=20) and by using Er,Cr:YSGG laser in Group 2 (n=20).

NCT ID: NCT03790202 Completed - Wound Heal Clinical Trials

VistaCare® in the Treatment of Wounds of the Lower Extremity

Start date: February 18, 2019
Phase:
Study type: Observational

Assessment of the safety and performance of the VistaCare® medical device in current medical practice in the treatment of acute and chronic lower limb wounds.

NCT ID: NCT03764943 Completed - Breast Cancer Clinical Trials

Immunonutrition and Carbohydrate Loading Strategies in Breast Reconstruction

Start date: February 1, 2019
Phase: Phase 3
Study type: Interventional

This study is designed to test the following hypothesis: patients undergoing immediate alloplastic and autologous breast reconstruction following mastectomy that receive preoperative immunonutrition will experience a reduction in wound complications in the 30-day postoperative period compared to a standard of care control group (retrospective chart review) of 264 (132 alloplastic + 132 autologous) consecutive breast reconstruction patients prior to 5/25/2018.

NCT ID: NCT03743987 Completed - Wound Heal Clinical Trials

The Effect of MTA and PRF Application in Periapical Lesions

Start date: December 20, 2016
Phase: N/A
Study type: Interventional

A total of 40 periapical lesions from the 33 patient undergoing apical surgery were randomly selected from December 2016-November 2017. Patients were informed about the surgical procedure and signed a consent form. Groups were divided in to 4; as control, MTA (mineral trioxide aggregate), PRF (platelet rich fibrin) and MTA+PRF groups. Apical resection was performed in all groups. No other interventions were made to the control group. Routine radiographs were taken in the 1st. 3th and 6th months. In the (approximately) 12th month of the procedures computerized tomography scans were taken. Primary healing of the periapical tissues were evaluated and the outcomes were measured. Patients have still been under control for the long term outcomes of the study.

NCT ID: NCT03703479 Completed - Wound Heal Clinical Trials

Effect of A-PRF After Removal of Wisdom Teeth

A-PRF
Start date: October 20, 2018
Phase: N/A
Study type: Interventional

To evaluate the healing effect of advanced platelet-rich fibrin (blood clot charged with growth factors) taken from the patient own blood on the extraction site.

NCT ID: NCT03698968 Completed - Wound Heal Clinical Trials

Performance, Safety and Efficacy of PICO Device.

Start date: November 6, 2018
Phase: N/A
Study type: Interventional

The study is being conducted to evaluate the safe and effective use of the PICO 7 system in surgically closed incision sites and wounds requiring closure by skin graft or flap as part of the PMCF plan for this product, for the purpose of continuing CE (Conformité Européene) Mark approval in accordance with MEDDEV 2.12-2

NCT ID: NCT03665272 Completed - Wound Heal Clinical Trials

The Evaluation of the Deepithelialized Gingival Graft Healing

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

The aim of this study was to compare of the effects of different fixation methods on deepithelialized gingival graft wound healing. Laser doppler flowmetry method was used to determine for blood perfusion changes. 40 patients were devided into two groups randomly and deepithelialized gingival graft procedure was performed and healings were evaluated by laser doppler flowmetry.

NCT ID: NCT03658278 Completed - Trauma Clinical Trials

Trauma Screening and Supplementation

Start date: March 15, 2018
Phase: N/A
Study type: Interventional

The purpose of the proposed study is twofold: 1) The investigators will evaluate ultrasound imaging to screen trauma patients to identify patients at increased risk of postoperative complications associated with sarcopenia. 2) The investigators will evaluate a commercially-available oral nutritional supplement that has previously been evaluated in critically-ill intensive care patients and shown benefit for decreasing complications including decreased wound healing complications, decreased pressure ulcers, decreased skeletal muscle loss due to immobilization, and decreased one-year mortality.

NCT ID: NCT03655158 Completed - Wound Heal Clinical Trials

The Effects of Ozone Therapy on Wound Healing

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

the aim of present study was to evaluate effects of ozone therapy on wound healing after gingivectomy and gingivoplasty operations as a model of secondary wound healing.. Twenty three systemically healthy individuals participated in this study. Ozone was applied immediately after surgery, at 1st day and 3rd day after gingivectomy surgery. In the photographs of the wounds, the difference in color were evaluated and measurements were performed at the baseline, 3rd, 7th, 14th days after surgery.

NCT ID: NCT03641053 Completed - Wounds and Injuries Clinical Trials

Honey Versus Povidone-iodine on Laceration Wounds

Start date: January 29, 2018
Phase: Phase 3
Study type: Interventional

This study evaluates healing time in usage of honey and povidone-iodine over paraffin gauze as dressings in the treatment of acute laceration wounds. In Indonesia, especially in rural area, where most of the resources is limited and modern dressings are expensive and hard-to-find. The investigators tried to find an alternative which was easier to find and could act as a substitute of modern wound dressing. The hypothesis of this study is honey and povidone-iodine could be a good substitute (or equal to) to paraffin gauze on acute laceration wounds. Honey is chosen because of its versatility and already well-known to be used as a chronic wound dressing. Povidone-iodine was chosen as another alternative because it is still one of the most used substance in rural area as a wound dressing, but there is not enough study to support the usage of this substance. Paraffin gauze was chosen as a representative of modern wound dressing because it fulfilled the standard of wound dressing on acute wound, which is non-adherent and also moist.