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Wound Healing clinical trials

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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.

NCT ID: NCT01008111 Withdrawn - Wound Healing Clinical Trials

Wound Healing of Incisional Wounds for Bilateral Hernia Repair

Start date: October 2009
Phase: Phase 1
Study type: Interventional

The purpose of this research study is to test the safety of an oxygen producing gel (produced by combining baking soda and hydrogen peroxide) and see what effects (good and bad) it has on skin incisions in children. Baking soda and hydrogen peroxide have been approved by the US Food and Drug Administration (FDA), but have not been approved for use in this manner. It is hypothesized that a combination of sodium bicarbonate and hydrogen peroxide may enhance wound healing of incisional wounds for bilateral hernia repair.

NCT ID: NCT01004055 Completed - Wound Infection Clinical Trials

Efficacy Study of a Bioelectric Dressing to Treat Wounds Caused by Curettage and Electrodesiccation

Start date: July 2008
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether a bioelectric wound dressing, a silver-coated dressing, or a silver-foam dressing are effective in the treatment of wounds resulting from curettage and electrodesiccation of skin lesions.

NCT ID: NCT00996463 Completed - Wound Healing Clinical Trials

Rationales for Wound Care Management in Old World Cutaneous Leishmaniasis Patients

LEICO
Start date: January 2010
Phase: Phase 2
Study type: Interventional

The rationales of a clinical trial comparing intralesional antimonial therapy versus wound care management in patients with old world cutaneous leishmaniasis (OWCL) are the following: 1. The effectiveness of the current mainstay treatment with intralesional antimonials for CL is subject to discussion, especially in L. major lesions which are predominant in Northern Afghanistan 2. The importance of wound care management in patients with OWCL has been emphasized by Gonzalez et al. (2008) and its efficacy is confirmed in the Kabul trial with L. tropica patients. Parallel to the clinical efficacy the trial investigates the cost-effectiveness and -utility of the treatment options under study.

NCT ID: NCT00984646 Completed - Wound Healing Clinical Trials

Investigation Into the Scar Reduction Potential of Prevascar (Interleukin-10)

Start date: April 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study was to investigate the scar-reducing properties of eight doses of intradermal Prevascar (IL-10).

NCT ID: NCT00984581 Completed - Wound Healing Clinical Trials

Safety and Efficacy Study of Avotermin (Juvista) in Female Subjects

Start date: April 2003
Phase: Phase 1/Phase 2
Study type: Interventional

To assess safety and toleration, systemic exposure and anti-scarring potential of intradermal avotermin (Juvista) in young females.