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A Pilot Study to Explore the Role of Gut Flora in Myasthenia Gravis

P

ProgenaBiome

Status

Withdrawn

Conditions

Myasthenia Gravis
Myasthenia Gravis, Generalized

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT04224506
PRG-039

Details and patient eligibility

About

This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records.

Full description

The goal of this Research Study is to better understand how the genetic information in subject's microbiome correlates to Myasthenia Gravis.

Sex

All

Volunteers

No Healthy Volunteers

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

Trial design

0 participants in 1 patient group

Myasthenia Gravis
Description:
Patients who have been diagnosed with Myasthenia Gravis.
Treatment:
Other: No intervention

Trial contacts and locations

1

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Central trial contact

Sabine Hazan, MD; Jordan Daniels, MS

Data sourced from clinicaltrials.gov

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