Antifungal Agents and Infrared Thermotherapy Alone or in Combination in the Treatment of Sporotrichosis
NCT06300138 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150
Last updated 2025-08-13
Summary
Sporotrichosis is a chronic granulomatous mycosis caused by sporothrix complex. The course of sporotrichosis is always prolonged and even life-threatening, the treatment of this disease in an important scientific problem to be solved. The investigators previously found the predominance of subtype M2 macrophage which play an anti-inflammatory role in the lesions of sporotrichosis, the predominance of M2 macrophage may be responsible for the persistence of sporotrichosis; the investigators also found that local hyperthermia is effective in the treatment of sporotrichosis and hyperthermia treatment can activate the CRAC calcium channel in macrophages which triggers pro-inflammatory type M1 polarization and subsequent killing of sporothrix, however, the mechanism still calls for further investigation. The investigators hypothesize that hyperthermia leads to the activation of CRAC channels resulting in profound Ca2+ influx and Ca2+ upregulates NLRP3 inflammasome expression through inducing Nrf2 activation, then NLRP3 overexpression triggers M1 polarization and subsequent killing of sporothrix. Furthermore, the activation of Nrf2 upregulates STIM1 expression which forms a positive feedback for M1 type polarization of macrophages and further subsequent killing of sporothrix. The purpose of this project is to identify the hypothesis that hyperthermia could treat sporotrichosis by promoting pro-inflammatory type M1 polarization in macrophages, the mechanism by which hyperthermia could treat sporotrichosis is local hyperthermia could led to STIM1/CRAC calcium channel activation mediated calcium ions/Nrf2/NLRP3 induced M1 macrophages polarization and subsequent killing of sporothrix. The hypothesis will be identified at the cellular level, at the animal model level and at the clinical specimens level. The investigators believe that the project will guide the application of hyperthermia in the treatment of sporotrichosis and provide a new basis of theory and practice after the investigators achieving these goals.
Conditions
- Sporotrichosis
Interventions
- DRUG
-
Itraconazole
oral itraconazole (children less than 15 years old 6 mg/kg/d; adult patients: 200 mg/d) for a total course of 3-6 months
- DEVICE
-
Infrared thermotherapy apparatus
infrared hyperthermia device for 3 consecutive days (times / day), each treatment for 30 minutes After two weeks (14 days), the lesions of the same target were treated continuously for 2 days (times per day), and then once a week for 2 consecutive times, the method was the same as before. After 7 times of treatment, the study physician decided whether to continue treatment n times after 1-2 weeks (n ≥ 0) according to the recovery of the subjects.
- OTHER
-
Itraconazole and Infrared thermotherapy apparatus
oral itraconazole (children less than 15 years old 6 mg/kg/d; adult patients: 200 mg/d) for a total course of 3-6 months, while infrared hyperthermia device for 3 consecutive days (times / day), each treatment for 30 minutes After two weeks (14 days), the lesions of the same target were treated continuously for 2 days (times per day), and then once a week for 2 consecutive times, the method was the same as before. After 7 times of treatment, the study physician decided whether to continue treatment n times after 1-2 weeks (n ≥ 0) according to the recovery of the subjects.
Sponsors & Collaborators
-
First Hospital of China Medical University
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-03-15
- Primary Completion
- 2026-12-31
- Completion
- 2026-12-31
Countries
- China
Study Locations
More Related Trials
-
Use of Essential Oils as Natural Therapies
NCT05777525 ·Status: COMPLETED ·Phase: PHASE3
-
Drug-Drug Interaction Study of Itraconazole With GST-HG171/Ritonavir in Healthy Participants
NCT06087055 ·Status: COMPLETED ·Phase: PHASE1
-
A Clinical Trial to Evaluate the Effect of Itraconazole and Rifampicin on ABSK021
NCT06089733 ·Status: COMPLETED ·Phase: PHASE1
-
A Study in Healthy Men to Test Whether Itraconazole Influences the Amount of BI 1584862 in the Blood
NCT06041438 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Effect of 2 Drugs on the Pharmacokinetics of BMS-986205 in Healthy Subjects
NCT03346837 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy of Self Vs. Physician Application of Triamcinolone-Econazole in Otomycosis
NCT06431542 ·Status: COMPLETED ·Phase: PHASE4
-
Comparative Study Between Pulse Therapy With Oral Itraconazole Versus Continuous Oral Terbinafine Therapy for Treatment of Onychomycosis
NCT05578950 ·Status: COMPLETED ·Phase: PHASE1
-
Treatment of Mycosis Fungoides With Hypericin Ointment and Visible Light
NCT05872854 ·Status: COMPLETED ·Phase: PHASE2
-
Evaluation of Two Dermatophyte qPCR Kits on Skin and Keratinous Samples.
NCT07270471 ·Status: COMPLETED
-
Comparative Study Between Pulsed and Continuous Itraconazole for the Treatment of Onychomycosis
NCT05567484 ·Status: COMPLETED ·Phase: PHASE1
-
Effect of Administration of Itraconazole on the Pharmacokinetics of S-309309 in Healthy Participants
NCT06106334 ·Status: COMPLETED ·Phase: PHASE1
-
SVT-15652 Otic Solution for the Treatment of Otomycosis.
NCT03686397 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Investigate the Effect of CYP3A Inhibition on the Pharmacokinetics of RG1662 in Healthy Subjects
NCT02470832 ·Status: COMPLETED ·Phase: PHASE1
-
Comparison Between Continuous and Pulse Itraconazole in Tinea Capitis in Children
NCT07184203 ·Status: RECRUITING ·Phase: NA
-
Safety & Efficacy Study of HTU-520 in the Treatment of Distal Subungual Onychomycosis of the Toenail
NCT01400594 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of Product S2G6T-1in Patients With Symptomatic Inflammatory Interdigital Tinea Pedis
NCT02842021 ·Status: TERMINATED ·Phase: PHASE2
-
A Study to See if Low Level Laser Light Can Help to Treat Toenail Fungus
NCT03066336 ·Status: WITHDRAWN ·Phase: NA
-
Ketoconazole in Treating Participants With Ongoing EGFR Inhibitor-Induced Rash
NCT03471364 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
The Comparative Assessment of Mycological Efficacy, Safety, Recurrence, and Cost-effectiveness of Selenium Sulfide 1.8% Shampoo Versus Ketoconazole 2% Shampoo in Pityriasis Versicolor: a Double-blind Randomized Controlled Trial
NCT04007237 ·Status: COMPLETED ·Phase: PHASE4
-
Safety and Efficacy of Nitrogen Mustard in Treatment of Mycosis Fungoides
NCT00168064 ·Status: COMPLETED ·Phase: PHASE2
-
Isotretinoin In Preventing Recurrences In Chronic Recurrent Dermatophytosis
NCT03471455 ·Status: UNKNOWN ·Phase: PHASE2
-
Effect of Itraconazole on the Pharmacokinetics of SHR6390 in Healthy Subjects
NCT04423601 ·Status: COMPLETED ·Phase: PHASE1
-
A Itraconazole Effect Study of SHR2554 on Healthy Chinese Adult Subjects
NCT04627129 ·Status: COMPLETED ·Phase: PHASE1
-
Comparison of Efficacy of Single Oral Dose Fluconazole and Itraconazole in Patients With Pityriasis Versicolor
NCT05862714 ·Status: COMPLETED ·Phase: PHASE1
-
Antifungal Drugs in Treatment of Onychomycosis
NCT03171584 ·Status: UNKNOWN ·Phase: PHASE3