To look for any improvement or decline of a patients status after undergoing surgical removal of thymus by the use of instruments designed to be used through small incisions made on chest.
Not Applicable
- Conditions
- Health Condition 1: G700- Myasthenia gravis
- Registration Number
- CTRI/2020/06/025612
- Lead Sponsor
- All India Institute of Medical Sciences New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with Non-Thymomatous Myasthenia Gravis
Patients whose disease is well controlled on medications
Exclusion Criteria
Patients with Non-Thymomatous Myasthenia Gravis not willing to give consent to participate in this study
Patients with Non-Thymomatous Myasthenia Gravis not fit for General Anesthesia.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary:To assess the mid and long term neurological outcomes in non thymomatous myasthenia gravis following minimally invasive surgery.Timepoint: At 6 monthly intervals post surgery till completion of thesis
- Secondary Outcome Measures
Name Time Method To assess the quality of life of patients after thymectomy by the use of MG-QOL15r and MG-ADL asssessment scales.Timepoint: At 6 monthly intervals post surgery till completion of thesis