Advanced in Stevens-Johnson Syndrome

Dr. James Holmes

Family Medicine
Office
525 N Tryon St, 
Charlotte, NC 
Advanced in Stevens-Johnson Syndrome
Office
525 N Tryon St, 
Charlotte, NC 
OverviewInsuranceLocationsClinical ResearchSimilar Doctors

Overview

James Holmes is a primary care provider, practicing in Family Medicine in Charlotte, North Carolina. Dr. Holmes is rated as an Advanced provider by MediFind in the treatment of Stevens-Johnson Syndrome. His top areas of expertise are Erythema Multiforme, Stevens-Johnson Syndrome, Scalded Skin Syndrome, Sepsis, and Fasciotomy.

His clinical research consists of co-authoring 70 peer reviewed articles and participating in 7 clinical trials. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 4 articles in the study of Stevens-Johnson Syndrome.

Specialties
Family Medicine
Licenses
Family Medicine in SC
Languages Spoken
English
Gender
Male

Insurance

Accepted insurance can change. Please verify directly with the provider.

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Locations

Office
525 N Tryon St, Charlotte, NC 28202

Clinical Research

Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Providers who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.

7 Clinical Trials

CONTINUED ACCESS PROTOCOL: Demonstration of the Safety and Effectiveness of ReCell® Combined With Meshed Skin Graft for Reduction of Donor Area in the Treatment of Acute Burn Injuries
CONTINUED ACCESS PROTOCOL: Demonstration of the Safety and Effectiveness of ReCell® Combined With Meshed Skin Graft for Reduction of Donor Area in the Treatment of Acute Burn Injuries
Enrollment Status: Completed
Publish Date: July 30, 2024
Intervention Type: Device
Study Phase: Not Applicable
Continued Access Protocol: A Prospective, Multicenter, Single-Arm, Observational Study of the Safety and Clinical Performance of RES (Regenerative Epithelial Suspension) Prepared With the ReCell® Device Combined With Meshed Skin Graft in the Treatment of Acute Burn Injuries
Continued Access Protocol: A Prospective, Multicenter, Single-Arm, Observational Study of the Safety and Clinical Performance of RES (Regenerative Epithelial Suspension) Prepared With the ReCell® Device Combined With Meshed Skin Graft in the Treatment of Acute Burn Injuries
Enrollment Status: Completed
Publish Date: July 30, 2024
Intervention Type: Device
A Prospective Multicenter Randomized Controlled Clinical Study to Investigate the Safety and Effectiveness of RES® (Regenerative Epidermal Suspension) Prepared With the RECELL® Device Compared to Standard of Care Dressings for Treatment of Partial-thickness Burns in Infants, Children and Adolescents (Aged 1-16 Years)
A Prospective Multicenter Randomized Controlled Clinical Study to Investigate the Safety and Effectiveness of RES® (Regenerative Epidermal Suspension) Prepared With the RECELL® Device Compared to Standard of Care Dressings for Treatment of Partial-thickness Burns in Infants, Children and Adolescents (Aged 1-16 Years)
Enrollment Status: Terminated
Publish Date: July 30, 2024
Intervention Type: Device, Procedure, Combination product
Study Phase: Not Applicable
DeepView SnapShot Portable (DV-SSP): Device Training Study
DeepView SnapShot Portable (DV-SSP): Device Training Study
Enrollment Status: Completed
Publish Date: March 06, 2024
Intervention Type: Device
Effects of Enteral Glutamine Supplementation on Mortality and Infectious Morbidity in Severely Burned Patients: a Multi-center Pilot Trial
Effects of Enteral Glutamine Supplementation on Mortality and Infectious Morbidity in Severely Burned Patients: a Multi-center Pilot Trial
Enrollment Status: Unknown
Publish Date: December 30, 2021
Intervention Type: Dietary supplement
Study Phase: Phase 3
Open-label, Controlled, Randomized, Multicenter, Dose Escalation Study Evaluating the Safety, Tolerability, and Efficacy of Single or Multiple Applications of StrataGraft® Skin Tissue as an Alternative to Autografting Full-thickness Complex Skin Defects
Open-label, Controlled, Randomized, Multicenter, Dose Escalation Study Evaluating the Safety, Tolerability, and Efficacy of Single or Multiple Applications of StrataGraft® Skin Tissue as an Alternative to Autografting Full-thickness Complex Skin Defects
Enrollment Status: Terminated
Publish Date: August 03, 2021
Intervention Type: Biological, Procedure
Study Phase: Phase 2
A Phase III Open-label, Controlled, Randomized, Multicenter Study Evaluating the Efficacy and Safety of StrataGraft Skin Tissue in Promoting Autologous Skin Tissue Regeneration of Complex Skin Defects Due to Thermal Burns That Contain Intact Dermal Elements and for Which Excision and Autografts Are Clinically Indicated
A Phase III Open-label, Controlled, Randomized, Multicenter Study Evaluating the Efficacy and Safety of StrataGraft Skin Tissue in Promoting Autologous Skin Tissue Regeneration of Complex Skin Defects Due to Thermal Burns That Contain Intact Dermal Elements and for Which Excision and Autografts Are Clinically Indicated
Enrollment Status: Completed
Publish Date: July 14, 2021
Intervention Type: Biological, Procedure
Study Phase: Phase 3
View 6 Less Clinical Trials

70 Total Publications

Is Burn Center Admission Necessary After Home Oxygen Ignition Injury?
Is Burn Center Admission Necessary After Home Oxygen Ignition Injury?
Journal: Journal of burn care & research : official publication of the American Burn Association
Published: May 06, 2025
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Areas of Expertise

MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.

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