Clinical Trials Logo

Wound Healing clinical trials

View clinical trials related to Wound Healing.

Filter by:

NCT ID: NCT01454310 Completed - Wound Healing Clinical Trials

An Acellular Epithelial Skin Substitute in Deep Partial-thickness Burns

Start date: November 2010
Phase: Phase 4
Study type: Interventional

The purpose of the study is to compare an acellular epithelial skin substitute with autologous split-thickness skin grafts (STSGs) in deep partial-thickness burns. The objective is to evaluate skin quality and scar formation by using subjective and objective burn scar assessments in order to present valuable data for another additional option of wound coverage in deep partial-thickness burns. The investigators hypothesized that the acellular epithelial skin substitute is at least not inferior to autologous skin grafts.

NCT ID: NCT01264588 Completed - Wound Healing Clinical Trials

The Effects of Topical Calcium Glycerophosphate on Surgical Wound Healing and Residual Scarring

TOPCGP-2008
Start date: April 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether topical application of calcium glycerophosphate will result in superior wound appearance and scar minimization.

NCT ID: NCT01264146 Completed - Wound Healing Clinical Trials

Hyperbaric Oxygen Therapy in Calcaneal Intraarticular Fractures: Can it Decrease the Soft-tissue Complication Rate?

HOCIF
Start date: April 2011
Phase: N/A
Study type: Interventional

This study aims to test the hypothesis that postoperative daily hyperbaric oxygen therapy (HBOT) decreases soft-tissue complication rate during the operative handling of intra-articular calcaneal fractures. Minor motivations: 1. To evaluate microcirculatory criteria of cutaneous tissue predicting emerging wound healing defects, 2. To identify patients at risk for soft-tissue complication after calcaneal plate osteosynthesis and to determine the optimal time point for operative intervention using these microcirculatory criteria preoperatively, 3. To evaluate the effect of HBOT on postoperative microcirculation, 4. To collect preliminary data to evaluate the economical impact of wound complications, with and without HBOT, 5. To identify a correlation between HBOT with expected limited soft-tissue complication rate and the clinical and radiographic outcome two years after surgery.

NCT ID: NCT01258270 Completed - Wound Healing Clinical Trials

Efficacy and Patient Satisfaction With AQUACEL® Ag Surgical Dressing Compared to Standard Surgical Dressing

Start date: December 2010
Phase: N/A
Study type: Interventional

The objective of this study is to determine the safety and effectiveness of the AQUACEL® Ag Surgical Dressing (treatment group) as compared to prepackaged island wound dressings consisting of traditional tape and gauze (control group) for total hip and total knee arthroplasty.

NCT ID: NCT01227759 Completed - Wounds Clinical Trials

Tyrosur® Gel-Investigation on Wound Healing Efficacy

Start date: September 2010
Phase: Phase 2
Study type: Interventional

This IIa study with intraindividual comparison of treated versus untreated to assess the wound healing efficacy of Tyrosur® Gel after experimental impairment of the skin using an abrasive wound healing model.

NCT ID: NCT01145820 Completed - Trauma Clinical Trials

Fruit And Vegetables and OUtcomes After Removal of Impacted TEeth

FAVOURITE
Start date: June 2010
Phase: N/A
Study type: Interventional

The proposed study will test the following hypotheses: 1. Pre-operative daily dual supplementation with Juice Plus+ (fruit & vegetable) for 11 weeks will result in reduced post-operative morbidity in terms of quality of life, pain and trismus after 1 week following surgical removal of lower third molars, when compared to placebo. 2. Pre-operative daily dual supplementation with Juice Plus+ (fruit & vegetable) for 11 weeks will reduce serum markers of oxidative stress, following surgical removal of lower third molars, when compared with placebo.

NCT ID: NCT01115218 Completed - Glaucoma Clinical Trials

The Influence of Anterior Chamber Fluid Mediators on the Success Rate of Trabeculectomy

Start date: October 2009
Phase:
Study type: Observational

The aim of the study is to investigate whether it is possible to predict the success of trabeculectomy in patients with glaucoma through the examination of mediators of wound healing in anterior chamber fluid. The success rate of trabeculectomy with mitomycin C in the literature is about 75%. This leads on the question why 25% of the patients received trabeculectomy are not sufficient treated and have not a long-term IOP reduction. Precisely this question is to be examined by the study.

NCT ID: NCT01078467 Completed - Wounds and Injuries Clinical Trials

The Molecular Anatomy of Oral Wound Healing

Start date: February 2, 2010
Phase:
Study type: Observational

Background: - Two important properties distinguish the healing process of skin wounds from that of wounds of the mucous membranes of the mouth (oral mucosa). Although the skin and the oral mucosa tissues are similar in nature, oral mucosa have more rapid healing and a lack of scar tissue formation. However, oral wound healing in general has been poorly studied, and more information is needed to determine how specific aspects of the oral environment affect the healing process. - Researchers are interested in identifying various factors that contribute to oral wound healing. Studying this process would help researchers explore procedures to accelerate the healing of critically-sized oral lesions formed by trauma, surgery, radiation therapy, infection, and other damage to the mouth. In addition, research into scar-free healing could be applied to other mucosal sites to promote healing and minimize unsightly scars that may compromise the tissue. Objectives: - To identify the specific factors that enable rapid and nearly scar-free healing of oral mucosa. Eligibility: - Healthy male volunteers between 18 and 40 years of age. - Regular cigarette, cigar, and pipe smokers; occasional smokers who smoke more than 1 day a week or have smoked in the prior month; users of chewing tobacco or betel nut; and heavy drinkers (three or more alcoholic drinks per day) will be excluded. Design: - Participants will have a medical history and examination, and will provide blood samples at the start of the study. - Participants will provide oral mucosa samples from the inside of the cheek, taken using a dermal punch. At the same time, participants will provide skin biopsy samples of approximately the same size. After the skin and oral mucosa samples are taken, participants will be divided into three groups for follow-up procedures. - Group 1: No further samples will be collected. This group will help document the normal healing process. - Group 2: A second, slightly larger biopsy, which will include the area of the first biopsy, will be taken on day 3. Both skin and oral mucosa biopsies will be taken. - Group 3: A second, slightly larger biopsy will be taken on day 6, in a similar way as described for Group 2. Both skin and oral mucosa biopsies will be taken. - Wounds will be photographed with a digital camera on days 3, 6, 9, 13, and 15; and the healing will be monitored at the scheduled clinic visits.

NCT ID: NCT01061502 Completed - Burns Clinical Trials

Efficacy Study of a Bioelectric Dressing to Treat Skin Graft Donor Site Wounds

Start date: September 2009
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether the use of a bioelectric wound dressing is effective in the healing of skin graft donor site wounds.

NCT ID: NCT01022216 Completed - Wound Healing Clinical Trials

Efficacy Study of a Bioelectric Dressing Used With Negative Pressure Wound Therapy to Treat Diabetic and Pressure Ulcers

Start date: August 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether a bioelectric wound dressing, used in conjunction with Negative Pressure Wound Therapy (NPWT), is effective in the treatment of diabetic and pressure ulcers of the foot.