Clinical trial · Observational
A Pilot Study to Explore the Role of Gut Flora in Myasthenia Gravis
A Non-Interventional Pilot Study to Explore the Role of Gut Flora in Myasthenia Gravis
NCT04224506CI-TRIAL-00090595withdrawnClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Company shifted focus
Summary
Brief summary (as posted)
This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Myasthenia Gravis | — | UNRESOLVED | — |
| Myasthenia Gravis, Generalized | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| No intervention | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Myasthenia Gravis
- description
- Patients who have been diagnosed with Myasthenia Gravis.
- interventionNames
- Other: No intervention
Primary outcomes (1)
- measure
- Correlation of Microbiome to Disease via Relative Abundance Found in Microbiome Sequencing
- timeFrame
- Three years
- description
- Relative abundance of bacterial classes within taxonomic phyla and, more broadly, within their domain will be analyzed by sequencing the gut microbiome. These data will then be categorized with Myasthenia Gravis.
Eligibility
Eligibility (as posted)
- Sex
- All
Show eligibility criteria text
Inclusion Criteria: 1. Signed informed consent, demonstrating that the patient understands the procedures required for the study and the purpose of the study a. May be signed by parent or legal guardian in the case of minor or adult unable to provide consent 2. Male or female of all ages. 3. Diagnosis of Myasthenia Gravis by a physician Exclusion Criteria: 1. Refusal to sign informed consent form 2. History of bariatric surgery, total colectomy with ileorectal anastomosis or proctocolectomy. 3. Postoperative stoma, ostomy, or ileoanal pouch 4. Participation in any experimental drug protocol within the past 12 weeks 5. Treatment with total parenteral nutrition
References
Publications (0)
Data not yet available
No reference posted for this study.