The Novel Electrolyzed Water Spray Treatment Discomfort, Redness and Swelling of the Skin Surrounding the Wound
NCT05792306 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2024-04-25
Summary
The purpose of this study is to test whether the reduction of the sense of discomfort and redness and swelling of the skin surrounding the wound of patients by use of the novel electrolyzed water spray will relieve the inflammation of the skin.
Conditions
- Skin Injury
Interventions
- DEVICE
-
The novel electrolyzed water spray
The researcher use electrolyzed water to treat the diseased area, two times a day, for 5 days. The trial consists of 5 study visits (day 1-day 5). The reduction in the disease area of discomfort, redness and swelling evaluation and adverse event assessments will be performed at each visit. Safety analysis will be assessed based on the reports of adverse events during the study.
- DEVICE
-
The saline spray
The researcher use saline to treat the diseased area, two times a day, for 5 days. The trial consists of 5 study visits (day 1-day 5). The reduction in the disease area of discomfort, redness and swelling evaluation and adverse event assessments will be performed at each visit. Safety analysis will be assessed based on the reports of adverse events during the study.
Sponsors & Collaborators
-
Dove Medical Press Ltd
lead NETWORK
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-01-29
- Primary Completion
- 2023-07-15
- Completion
- 2024-03-10
Countries
- China
Study Locations
More Related Trials
-
Clinical Evaluation of the SNaP Wound Care System
NCT01113658 ·Status: WITHDRAWN ·Phase: NA
-
Effect of Regulated Oxygen-Enriched Negative Pressure Therapy (RO-NPT) On Soft Tissue Wound Repair
NCT02357628 ·Status: UNKNOWN
-
A Prospective, Open Label, Multicenter Trial for Evaluating the Efficacy of Treating and Managing Wounds in Elderly Population in Specialized Nursing Facilities Using RD1
NCT04577183 ·Status: TERMINATED ·Phase: NA
-
Activated Carbon Interphase Effect on Surgical Incisions vs.Two Common Wound Dressings
NCT04038671 ·Status: WITHDRAWN ·Phase: NA
-
Effect of Combined Red and Near Infrared Light-emitting Diode (LED) Therapy on Tissue Regeneration Post Laser Treatment
NCT04834817 ·Status: COMPLETED ·Phase: NA
-
Tap Water Versus Normal Saline for Wound Irrigation
NCT01564342 ·Status: COMPLETED ·Phase: NA
-
CO2 Laser Revision for Burn Related Donor Site Scars
NCT04456127 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Therapeutic Effect of the Wireless Micro Current Stimulation in Pediatric Deep Dermal Burns and Scald Injuries
NCT02712580 ·Status: UNKNOWN ·Phase: NA
-
Observation of the Comfort and Efficacy of CO2 Laser Combined With Cryo 6 for Burn or Linear Scars.
NCT05555602 ·Status: UNKNOWN ·Phase: NA
-
Pulsed-dye Laser Treatment Prior to Surgical Excision
NCT02458976 ·Status: UNKNOWN ·Phase: NA
-
Surgical Scar Treatment With the Pulsed Dye Laser in Combination With a CO2 Laser
NCT02898350 ·Status: COMPLETED ·Phase: NA
-
Laser Treatment for the Improvement of Scars and Scleroderma
NCT04567537 ·Status: TERMINATED ·Phase: NA
-
In-vivo Analysis of a Fractional CO2 Laser System (eMatrixCO2) Intended for Treatment of Soft Tissue
NCT01026662 ·Status: UNKNOWN
-
Efficacy and Safety of High Absorption Pad in Split-thickness Skin Graft Donor Site Wound
NCT04299126 ·Status: UNKNOWN ·Phase: NA
-
Aloe Vera vs Paraffin Tulle Dressings for Pain Management in Split Thickness Skin Graft Donor Sites
NCT07057557 ·Status: RECRUITING ·Phase: NA
-
Patient Satisfaction and Recovery Outcomes Associated With Perioperative ELIXIR MD Use
NCT07311889 ·Status: ENROLLING_BY_INVITATION
-
Laser Treatment in Early Wound Healing to Promote Physiological Skin Remodeling
NCT03253484 ·Status: UNKNOWN ·Phase: NA
-
Effect of Lidocaine and Adrenaline Soaked Gauze Versus Normal Saline Soaked at Skin Graft Donor Site of Thigh
NCT04344483 ·Status: COMPLETED ·Phase: NA
-
Efficacy of Spray Silicone in Alteration of Burn Scar
NCT01075165 ·Status: WITHDRAWN ·Phase: NA
-
Feasibility Study: Enzymatic Debridement in Patients With Partial Thickness Burns
NCT00898521 ·Status: COMPLETED ·Phase: PHASE2
-
EO2 Oxygen Delivery To Study Success Rate of Surgically Closed Wounds
NCT03960463 ·Status: COMPLETED ·Phase: NA
-
A Postmarket Clinical Follow Up Study (PMCF) to Evaluate the Safety and Performance of VERIFORTE/Granudacyn® Med Wound Irrigation Solution.
NCT06083740 ·Status: COMPLETED
-
Comparison Between Drinking Water and Normal Saline in Irrigating Traumatic Wound
NCT06304272 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
A Study of a Novel Silicone Dressing to Minimize Scar Formation
NCT01399099 ·Status: COMPLETED ·Phase: NA
-
Stretch Marks on Abdomen
NCT03750422 ·Status: UNKNOWN ·Phase: NA