Resin Salve Versus Honey Treatment in Wound Care

Status Completed

Clinical Trial Summary

In recent years, salve prepared from Norway spruce (Picea abies) resin and refined honey from manuka myrtle (Leptospermum scoparium), has successfully been used in medical context to treat both acute and chronic surgical wounds. The objective of this prospective, randomized and controlled clinical trial is to investigate healing rate and healing time of surgical wounds in patients, who have undergone peripheral vascular surgery, and whose complicated wounds are candidate for topical treatment with the resin or honey. In addition, factors contributing with delayed wound healing, antimicrobial properties, safety and cost-effectiveness of the resin salve and medical honey will be analyzed.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01868412
Study type	Interventional
Source	Kuopio University Hospital
Contact
Status	Completed
Phase	N/A
Start date	May 2013
Completion date	January 2016

View Details

See also
Status	Clinical Trial	Phase
Recruiting	`NCT02905955` - Vacuumtherapy After Venous Hybrid Procedures	Phase 4
Not yet recruiting	`NCT02868372` - Swabbing of Subcutaneous Tissues of Cesarean Section Wounds With Povidone Iodine	N/A
Enrolling by invitation	`NCT02559453` - Outcomes for 2 Operations Versus ≥ 3 Operations in Infected Wounds	N/A
Completed	`NCT02744144` - Wound Bacterial Microbiota and Their Antibiotic Resistance	N/A
Active, not recruiting	`NCT01939145` - Comparing Outcomes for Prontosan Versus Normal Saline for Negative Pressure Wound Therapy With Instillation	Phase 4
Completed	`NCT00998907` - PDS*Plus and Wound Infections After Laparotomy	N/A
Completed	`NCT01141335` - Polypropylene Mesh Versus Polytetrafluoroethylene (PTFE) Mesh in Inguinal Hernia Repair	Phase 4
Terminated	`NCT00654641` - Prevention of Wound Complications After Cesarean Delivery in Obese Women Utilizing Negative Pressure Wound Therapy	N/A
Completed	`NCT00576745` - A Comparison Of The 3M TM S Surgical Skin Closure System To The Standard Vicryl Suture Closure of Sternotomy Incisions During Cardiac Surgery	Phase 1
Completed	`NCT00402727` - Comparison of Sequential IV/PO Moxifloxacin With IV Piperacillin/Tazobactam Followed by PO Amoxicillin/Clavulanic Acid in Patients With a Complicated Skin and Skin Structure Infection	Phase 3
Recruiting	`NCT00150852` - Prevention of Gastrostomy-Related Wound Infection by Vancomycin in Carriers of Methicillin-Resistant Staphylococcus Aureus.	Phase 2
Not yet recruiting	`NCT03872544` - Short Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds
Recruiting	`NCT04596124` - Effectiveness and Tolerability of Fitostimoline Plus Cream and Gauze vs Connettivina Bio Plus Cream and Gauze	N/A
Active, not recruiting	`NCT04584957` - Prophylactic Negative Pressure Wound Therapy (VAC) in Gynecologic Oncology (G.O.)	N/A
Recruiting	`NCT03960970` - Two-drug Antibiotic Prophylaxis in Scheduled Cesarean Deliveries	Phase 2
Enrolling by invitation	`NCT03880188` - Long Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds
Completed	`NCT02018094` - The Amputation Surgical Site Infection Trial (ASSIT)	Phase 4
Terminated	`NCT03269968` - Use of Negative Pressure Wound Therapy in Morbidly Obese Women After Cesarean Delivery	N/A
Enrolling by invitation	`NCT02945761` - High Concentration of Sugar Solution Irrigation Promotes the Healing of Infected Wound	N/A
Not yet recruiting	`NCT02882360` - Kerlix for Pregnant Women With Elevated BMI to Prevent Wound Infection by 6 Weeks Post Partum	Phase 4