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Active clinical trials for "Wound Infection"

Results 91-100 of 354

The Effect of Vitamin C on Wound Healing In Mandibular Fracture Patients

Vitamin C DeficiencySmoking14 more

The goal of this study is to perform a randomized clinical trial to assess the effects of vitamin C versus placebo on wound healing in mandibular fracture patients.

Completed8 enrollment criteria

Surgical Adhesive Drapes for Prevention and Healing of Wound Infections After Total Hip Arthroplasty...

Hip Replacement

The purpose of this study is to support the rational use of iodophor-impregnated surgical adhesive drapes for preventing wound infections after total hip arthroplasty.

Completed12 enrollment criteria

Local Application of Ozone Gas for Infected Ulcers

UlcerWound Infection

This study evaluates the efficacy of local application of ozone gas in healing of infected ulcers. Half the participants received conventional treatment with placebo generator and the other half received conventional treatment with ozone generator.

Completed9 enrollment criteria

Activated Carbon Interphase Effect on Biofilm and Total Bacterial Load

Wound Infection

The purpose of this randomized, prospective study is to evaluate how this activated carbon dressing affects the total bacterial load and biofilm in a wound bed in wounds of the lower extremity and foot. We anticipate that the use of Zorflex® Activated Carbon Cloth dressing will maintain the bacterial burden in the wound bed below the level of critical colonization, with potential secondary benefits of pain reduction, decrease in inflammation, and control of odor. Wound bed healing progression/acceleration also will be assessed.

Completed22 enrollment criteria

Local Wound Infiltration Versus Caudal Block on Wound Infection and Healing in Paediatrics Inguinal...

Healing Surgical Wounds

The aim of the present study is to assess effect of local wound infiltration in comparison with caudal block by bupivacaine 0.25% after inguinal herniotomy in pediatrics on: Wound infection and healing (primary outcome) and postoperative analgesia (secondary outcome).

Completed7 enrollment criteria

A Phase I/II Double-Blind, Randomized, Controlled Study to Evaluate the Safety and Efficacy of RUT058-60...

Postoperative Wound Infection-deepPost Operative Wound Infection

This is a double-blind, randomized, parallel-group, controlled, multi-center study to evaluate the safety and efficacy of RUT058-60 (Group A) as an intra-cavity lavage compared to sterile saline (Group B) in adult subjects undergoing abdominal surgery.

Terminated30 enrollment criteria

V.A.C. VeraFlo™ Instillation Therapy vs V.A.C. Ulta™ Therapy on Biofilm in Chronically Infected...

Lower Extremity Wound InfectedVenous Stasis Ulcers

This study would like to determine if using negative pressure wound therapy with an instillation of .125% Dakins is more effective than using negative pressure wound therapy alone on biofilm removal, disruption and elimination in chronically infected lower extremity wounds.

Completed16 enrollment criteria

Single Dose vs. Two Dose Regimen of Dalbavancin for the Treatment of Acute Bacterial Skin and Skin...

AbscessWound Infection2 more

To compare the efficacy of treatment with a single dose of dalbavancin 1500 mg to treatment with a two dose regimen of dalbavancin (1000 mg on Day 1 followed by 500 mg on Day 8) in participants with known or suspected Gram-positive acute bacterial skin and skin structure infections (ABSSSI) at 48 -72 hours after initiation of treatment.

Completed32 enrollment criteria

The Risk of Postoperative Wound Complications Following the Use of Negative Pressure Wound Therapy...

Breast CancerWound Complication3 more

To evaluate the risk of postoperative wound complications following the use of Avelle negative pressure wound therapy in patients undergoing mastectomy and flap fixation, which might serve as a basis for a randomized controlled trial

Completed7 enrollment criteria

Negative Pressure Dressing Therapy in Soft Tissue Sarcoma Surgery

SarcomaWound Infection

This randomised controlled trial aims to evaluate the difference in surgical site infection following excision of soft tissue sarcomas. The intervention is a negative wound pressure therapy dressing for 120 hours, the control is standard absorbent dressings

Terminated6 enrollment criteria
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