MycetomaNCT04401969
Tissue Microenvironment Signatures of the Mycetoma Granuloma
An observational study of Mycetoma, run by University of Khartoum at 1 site in Sudan.
Trial summary
Mycetoma is the most neglected of the neglected tropical diseases. It is caused by certain fungi or bacteria. It is endemic in many tropical and subtropical regions and Sudan seems to be the mycetoma homeland. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Mycetoma
- How many people
- 28 participants
- Where
- 1 siteSudan
- Study dates
- 7 Mar 2019to 16 Apr 2019
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients are recruited from Soba University Hospital Mycetoma clinic 10 patients with eumycetoma lesions 12 patients with actinomycetoma lesions 6 patients with lesions of unknown causality
Who may be able to join
- Patients aged over 18 years with either small or advanced eumycetoma lesions with either small or advanced actinmycetoma lesions with lesions of unknown causality
Who cannot join
- <18 years of age Inability to provide informed consent Any other reason that in the opinion of the Investigator indicates the subject cannot comply with study protocol
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Studying the Tissue Microenvironment Signatures of the Mycetoma Granuloma
Mycetoma is the most neglected of the neglected tropical diseases. It is caused by certain fungi or bacteria. It is endemic in many tropical and subtropical regions and Sudan seems to be the mycetoma homeland. This chronic subcutaneous destructive and disabling inflammatory disease has many serious medical and socio-economic impacts on patients, community and health authorities. This work may suggest new therapeutic options for mycetoma that target the inflammatory pathogenic pathway and hence help in designing universal treatment options for mycetoma patients.
Two overlapping aims were investigated in this project to advance our overall goals:
- Profiling the immune/inflammatory signatures in the tissue microenvironment of fungus-induced mycetoma lesions
- Profiling the immune/inflammatory signatures in the tissue microenvironment of bacteria-induced mycetoma lesions.
Read the detailed description
Mycetoma is a chronic, specific, subcutaneous granulomatous, progressive and disfiguring inflammatory disease. It is caused by true fungi or by certain bacteria and hence it is usually classified into eumycetoma and actinomycetoma respectively. Madurella mycetomatis is the commonest eumycetoma causative agent, while Streptomyces somaliensis and Nocardia brasiliensis are the common causative organisms for actinomycetoma. The triad of a painless subcutaneous mass, sinuses formation and purulent or sero-purulent discharge that contains grains is pathognomonic of mycetoma. The inflammatory subcutaneous granuloma usually spreads to involve the skin and the deep structures, resulting in destruction, deformity and loss of function, occasionally it can be fatal. The foot and hand are the most frequently affected sites seen in 82% of cases. In endemic areas, other parts of the body may be involved such as the knee, arm, leg, head and neck, thigh and perineum. No age is exempted in mycetoma; however, it occurs more frequently in young adult men in the age range 20-40 years and almost 30% of reported patients were young students.
The true incidence and prevalence of mycetoma world-wide is not precisely known. It is interesting to note that most of the reported mycetoma data are related to hospital patients with advanced disease. This is attributed to the nature of mycetoma which is usually painless, slowly progressive and the late presentation of the majority of patients due to the poor health education, lack of health facilities and financial constraints.
The worldwide distribution of mycetoma varies widely. It is endemic in many tropical and subtropical regions and prevails in the mycetoma belt, which includes the countries of Sudan, Somalia, Senegal, India, Yemen, Mexico, Venezuela, Columbia, Argentina, and a few others. The African continent seems to have the highest burden and prevalence of the disease. It has also been extensively reported from India. However, mycetoma has been reported in many temperate regions as well. There are a few reports on mycetoma from the USA, Sri Lanka, Germany, Egypt, Turkey, Philippines, Japan, Lebanon, Thailand, Saudi Arabia, Tunisia and Iran.
The proper treatment of mycetoma depends mainly on accurate diagnosis. It is essential to identify the causative organism to the species level and the current tests for that are the classical grains culture, surgical biopsy histopathological examination and various molecular techniques such as PCR. Various imaging techniques such as conventional radiology, ultrasonography, CT scan and MRI are in use to determine the disease extend. Most of these tests and techniques are invasive, expensive and of low sensitivity and specificity. Furthermore, they are not available in the mycetoma endemic regions and hence there is a desperate need forth easy to use, field-friendly test to identify the causative agent.
The management of this distressing and devastating disease is disappointing. The treatment depends mainly on the aetiological agent, the site and extend of the disease. Until recently, the only available treatment for mycetoma was amputation or multiple mutilating disfiguring surgical excisions. Combined medical treatment in the form of antifungals for the eumycetoma and antibiotics and antimicrobial agents for actinomycetoma and various surgical excisions is the gold standard in mycetoma.
Reports on medical treatment in eumycetoma are scarce and inadequate. Over the years and till now, the treatment of eumycetoma was based on personal clinical experience and on the results of sporadic case reports, rather than controlled clinical trials. In general, massive surgical excisions or amputation of affected part is the treatment of choice for eumycetoma. Various antifungal agents have been tried with little success. This is perhaps surprising, as the eumycetoma causative agents are low-grade infective organisms and their eradication should be readily achieved by the administration of antifungal drugs. Generally, actinomycetoma is amenable to medical treatment with antibiotics and other chemotherapeutic agents. Combined drug therapy is always preferred to a single drug to avoid drug resistance and for disease eradication.
Medical treatment for both types of mycetoma must continue until the patient is clinically, radiologically, ultrasonically and cytologically cured. Recurrence is more common after an incomplete or irregular course of medical treatment. With patient non-compliance, there is a good chance for the organism to develop drug resistance.
The study was conducted at the Mycetoma clinic at the Mycetoma Research Centre (MRC), Khartoum Sudan. Patients were enrolled into the study after written informed consent was obtained in line with the Declaration of Helsinki.
Patients were categorized into three groups;
- Patients with eumycetoma lesions (n=10)
- Patients with actinomycetoma lesions (n=12)
- Patients with lesions of unknown causality (n=6)
Formalin fixation and paraffin embedding was performed at the MRC according to standard procedures.
Fine needle aspirates (FNA) was collected for flow cytometry at the same time and at the same location of the lesion in the body.
Aspirates were frozen at -80C for future analysis. Concurrently, 15 ml of blood was taken from each patient for immunological function assays.
Peripheral blood mononuclear cells were prepared using standard protocols and stored in liquid nitrogen till required.
5 ml of blood was collected in Paxgene tubes for transcriptomics analysis.
Immunohistochemistry Immunohistochemistry was performed at University of York, UK. Formalin fixed paraffin embedded (FFPE) sections were analysed using the 700 gene Nanostring PanCancer Immune Cell profiling panel to obtain a high level view of the immune/inflammatory signature.
Serial sections were subjected to highly multiplexed antibody staining using the Nanostring Digital Spatial Profiling system to obtain a comprehensive and spatially resolved insights into lesion microenvironment.
Candidate pan-mycetoma targets identified by these approaches were confirmed using immunofluorescent antibodies and RNA-fluorescent in situ hybridisation.
All data was recorded as digitised whole slide images for publication and archiving.
Antigen specific T cell responses T cells responses analysis were performed at Institute for Endemic Diseases, University of Khartoum.
Peripheral blood mononuclear cells (PBMCs) from patients and age and sex matched healthy control from endemic area were stimulated for 7 days with fungus and bacterial lysates. IFN, IL-17, IL-4 and IL-10 responses were determined by ELISPOT assay.
Flow cytometry on FNBs were performed with panels of antibodies to evaluate T cell and myeloid cell phenotype.
Whole blood transcriptomics Blood were collected into Paxgene and stored at - 80c. RNA were extracted from stored samples Full whole blood transcriptomic data was obtained by RNA-Seq.
Cytokine measurements in mycetoma aspirates were undertaken using commercially available ELISA kits.
- Conditions
- Mycetoma
- Medical subject headings
- Mycetoma
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Patients with eumycetoma lesions | Patients with eumycetoma lesions | |
| Patients with actinomycetoma lesions | Patients with actinomycetoma lesions | |
| Patients with lesions of unknown causality | Patients with lesions of unknown causality |
What is being measured
The primary outcome is the main question the study is designed to answer.
immune cell phenotypes
detection of immune cell phenotypes in mycetoma lesions
Measured: 24 months
antigen-specific t-cell responses
detection of t cell and myeloid cell phenotype in peripheral blood
Measured: 24 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 May 2020
- Study start7 Mar 2019
- Primary completion16 Apr 2019
- Study completion16 Apr 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for MycetomaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case only
- Time perspective
- Cross-sectional
- Enrolment
- 28 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Khartoum
- Sponsor type
- University, hospital or other
- Collaborators
- University of York
- Responsible party
- Principal investigator, Dr Mohamed Osman, University of Khartoum
- Investigators
- Mohamed Osman, PhD, Principal investigator, University of Khartoum
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04401969
- Sponsor's protocol ID
- Mycetoma Study
- Status last verified
- May 2020
- First submitted
- 19 May 2020
- Last updated
- 26 May 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Osman M, Ashwin H, Calder G, O'Toole P, Bakhiet SM, Musa AM, Kaye PM, Fahal AH. A conserved grain-associated immunosuppressive niche in Sudanese patients with mycetoma. PLoS Negl Trop Dis. 2026 Aug 17;20(8):e0014230. doi: 10.1371/journal.pntd.0014230. Online ahead of print.
PubMed 42607090
Study at a glance
From the registry record, last updated by the sponsor on 26 May 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Studying the Tissue Microenvironment Signatures of the Mycetoma Granuloma
- ClinicalTrials.gov ID
- NCT04401969
- Acronym / sponsor ID
- Mycetoma Study
- Conditions
- Mycetoma
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 28 participants (actual)
- Lead sponsor
- University of KhartoumUniversity, hospital or other
- Collaborators
- University of York
- Study start
- 7 Mar 2019 (actual)
- Primary completion
- 16 Apr 2019 (actual)
- Study completion
- 16 Apr 2019 (actual)
- First posted
- 26 May 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Mycetoma is the most neglected of the neglected tropical diseases. It is caused by certain fungi or bacteria. It is endemic in many tropical and subtropical regions and Sudan seems to be the mycetoma homeland. This chronic subcutaneous destructive and disabling inflammatory disease has many serious medical and socio-economic impacts on patients, community and health authorities. This work may suggest new therapeutic options for mycetoma that target the inflammatory pathogenic pathway and hence help in designing universal treatment options for mycetoma patients.
Two overlapping aims were investigated in this project to advance our overall goals:
- Profiling the immune/inflammatory signatures in the tissue microenvironment of fungus-induced mycetoma lesions
- Profiling the immune/inflammatory signatures in the tissue microenvironment of bacteria-induced mycetoma lesions.
Detailed description
Mycetoma is a chronic, specific, subcutaneous granulomatous, progressive and disfiguring inflammatory disease. It is caused by true fungi or by certain bacteria and hence it is usually classified into eumycetoma and actinomycetoma respectively. Madurella mycetomatis is the commonest eumycetoma causative agent, while Streptomyces somaliensis and Nocardia brasiliensis are the common causative organisms for actinomycetoma. The triad of a painless subcutaneous mass, sinuses formation and purulent or sero-purulent discharge that contains grains is pathognomonic of mycetoma. The inflammatory subcutaneous granuloma usually spreads to involve the skin and the deep structures, resulting in destruction, deformity and loss of function, occasionally it can be fatal. The foot and hand are the most frequently affected sites seen in 82% of cases. In endemic areas, other parts of the body may be involved such as the knee, arm, leg, head and neck, thigh and perineum. No age is exempted in mycetoma; however, it occurs more frequently in young adult men in the age range 20-40 years and almost 30% of reported patients were young students.
The true incidence and prevalence of mycetoma world-wide is not precisely known. It is interesting to note that most of the reported mycetoma data are related to hospital patients with advanced disease. This is attributed to the nature of mycetoma which is usually painless, slowly progressive and the late presentation of the majority of patients due to the poor health education, lack of health facilities and financial constraints.
The worldwide distribution of mycetoma varies widely. It is endemic in many tropical and subtropical regions and prevails in the mycetoma belt, which includes the countries of Sudan, Somalia, Senegal, India, Yemen, Mexico, Venezuela, Columbia, Argentina, and a few others. The African continent seems to have the highest burden and prevalence of the disease. It has also been extensively reported from India. However, mycetoma has been reported in many temperate regions as well. There are a few reports on mycetoma from the USA, Sri Lanka, Germany, Egypt, Turkey, Philippines, Japan, Lebanon, Thailand, Saudi Arabia, Tunisia and Iran.
The proper treatment of mycetoma depends mainly on accurate diagnosis. It is essential to identify the causative organism to the species level and the current tests for that are the classical grains culture, surgical biopsy histopathological examination and various molecular techniques such as PCR. Various imaging techniques such as conventional radiology, ultrasonography, CT scan and MRI are in use to determine the disease extend. Most of these tests and techniques are invasive, expensive and of low sensitivity and specificity. Furthermore, they are not available in the mycetoma endemic regions and hence there is a desperate need forth easy to use, field-friendly test to identify the causative agent.
The management of this distressing and devastating disease is disappointing. The treatment depends mainly on the aetiological agent, the site and extend of the disease. Until recently, the only available treatment for mycetoma was amputation or multiple mutilating disfiguring surgical excisions. Combined medical treatment in the form of antifungals for the eumycetoma and antibiotics and antimicrobial agents for actinomycetoma and various surgical excisions is the gold standard in mycetoma.
Reports on medical treatment in eumycetoma are scarce and inadequate. Over the years and till now, the treatment of eumycetoma was based on personal clinical experience and on the results of sporadic case reports, rather than controlled clinical trials. In general, massive surgical excisions or amputation of affected part is the treatment of choice for eumycetoma. Various antifungal agents have been tried with little success. This is perhaps surprising, as the eumycetoma causative agents are low-grade infective organisms and their eradication should be readily achieved by the administration of antifungal drugs. Generally, actinomycetoma is amenable to medical treatment with antibiotics and other chemotherapeutic agents. Combined drug therapy is always preferred to a single drug to avoid drug resistance and for disease eradication.
Medical treatment for both types of mycetoma must continue until the patient is clinically, radiologically, ultrasonically and cytologically cured. Recurrence is more common after an incomplete or irregular course of medical treatment. With patient non-compliance, there is a good chance for the organism to develop drug resistance.
The study was conducted at the Mycetoma clinic at the Mycetoma Research Centre (MRC), Khartoum Sudan. Patients were enrolled into the study after written informed consent was obtained in line with the Declaration of Helsinki.
Patients were categorized into three groups;
- Patients with eumycetoma lesions (n=10)
- Patients with actinomycetoma lesions (n=12)
- Patients with lesions of unknown causality (n=6)
Formalin fixation and paraffin embedding was performed at the MRC according to standard procedures.
Fine needle aspirates (FNA) was collected for flow cytometry at the same time and at the same location of the lesion in the body.
Aspirates were frozen at -80C for future analysis. Concurrently, 15 ml of blood was taken from each patient for immunological function assays.
Peripheral blood mononuclear cells were prepared using standard protocols and stored in liquid nitrogen till required.
5 ml of blood was collected in Paxgene tubes for transcriptomics analysis.
Immunohistochemistry Immunohistochemistry was performed at University of York, UK. Formalin fixed paraffin embedded (FFPE) sections were analysed using the 700 gene Nanostring PanCancer Immune Cell profiling panel to obtain a high level view of the immune/inflammatory signature.
Serial sections were subjected to highly multiplexed antibody staining using the Nanostring Digital Spatial Profiling system to obtain a comprehensive and spatially resolved insights into lesion microenvironment.
Candidate pan-mycetoma targets identified by these approaches were confirmed using immunofluorescent antibodies and RNA-fluorescent in situ hybridisation.
All data was recorded as digitised whole slide images for publication and archiving.
Antigen specific T cell responses T cells responses analysis were performed at Institute for Endemic Diseases, University of Khartoum.
Peripheral blood mononuclear cells (PBMCs) from patients and age and sex matched healthy control from endemic area were stimulated for 7 days with fungus and bacterial lysates. IFN, IL-17, IL-4 and IL-10 responses were determined by ELISPOT assay.
Flow cytometry on FNBs were performed with panels of antibodies to evaluate T cell and myeloid cell phenotype.
Whole blood transcriptomics Blood were collected into Paxgene and stored at - 80c. RNA were extracted from stored samples Full whole blood transcriptomic data was obtained by RNA-Seq.
Cytokine measurements in mycetoma aspirates were undertaken using commercially available ELISA kits.
Study design
- Observational model
- Case only
- Time perspective
- Cross-sectional
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Patients with eumycetoma lesions | – | –Patients with eumycetoma lesions |
| Patients with actinomycetoma lesions | – | –Patients with actinomycetoma lesions |
| Patients with lesions of unknown causality | – | –Patients with lesions of unknown causality |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients are recruited from Soba University Hospital Mycetoma clinic 10 patients with eumycetoma lesions 12 patients with actinomycetoma lesions 6 patients with lesions of unknown causality
Key inclusion criteria (1 listed)
- Patients aged over 18 years with either small or advanced eumycetoma lesions with either small or advanced actinmycetoma lesions with lesions of unknown causality
Key exclusion criteria (1 listed)
- <18 years of age Inability to provide informed consent Any other reason that in the opinion of the Investigator indicates the subject cannot comply with study protocol
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
immune cell phenotypes
Time frame: 24 months
detection of immune cell phenotypes in mycetoma lesions
antigen-specific t-cell responses
Time frame: 24 months
detection of t cell and myeloid cell phenotype in peripheral blood
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 26 May 2020.
- Derived from this study: PubMed 42607090Osman M, Ashwin H, Calder G, O'Toole P, Bakhiet SM, Musa AM, Kaye PM, Fahal AH. A conserved grain-associated immunosuppressive niche in Sudanese patients with mycetoma. PLoS Negl Trop Dis. 2026 Aug 17;20(8):e0014230. doi: 10.1371/journal.pntd.0014230. Online ahead of print.
- Individual participant dataSharing planned: No
Related trials for Mycetoma
Not yet recruiting
Early Detection and AI-Based Management of Skin-Related Neglected Tropical Diseases in Sub-Saharan Africa by Frontline Health Workers
Skin and Connective Tissue Diseases, Neglected Tropical Diseases
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Mohamed Osman, PhD principal investigator
University of Khartoum
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Mycetoma, run by University of Khartoum at 1 site in Sudan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 26 May 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Sudan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
immune cell phenotypes (time frame: 24 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04401969, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 26 May 2020; AzTrials last refreshed its copy on 7 Nov 2026.