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Cytotron® Delivered Rotational Field Quantum Nuclear Magnetic Resonance Therapy for Multiple Sclerosis

Phase 2
Conditions
Multiple Sclerosis
Interventions
Device: Cytotron
Registration Number
NCT01220830
Lead Sponsor
The Centre for Advanced Research & Development, India
Brief Summary

The purpose of the study is to evaluate the efficacy of RFQMR therapy in remyelination in cases of Multiple sclerosis.

The evaluation will be done based on MRI findings, by clinical/ neurological examination and by assessment of quality of life before and after completion of therapy.

Detailed Description

Transmembrane Potential (TMP) is one of the known cellular signalling pathways regulating synthesis of various proteins like those responsible for programmed cell death (e.g., p53 group) at the appropriate time in living cells. Many illnesses like cancer and degenerative diseases are linked to disturbances in transmembrane potential and protein transcription process.(Cone CD, 1970)

The protein responsible for production of myelin by the oligodendrocytes is Connexin 32. It has been established that in cases of Multiple Sclerosis (MS) this protein is not synthesized by the oligodendrocytes thus leading to non-repair of the demyelination process in the Central Nervous System (CNS) (Scherer SS et al., 1995; Sargiannidou I et al., 2009; Bondurand N et al., 2001). This causes the fibrotic damage and plaque formation and consequent signs and symptoms of MS. RFQMR therapy addresses this process of stimulation of Oligodendrocytes to synthesize Connexin 32 thus causing remyelination.

RFQMR therapy is delivered with CYTOTRON®. This device is a long body, wide bore machine with 864 guns, with near field antennae and parabolic reflector delivery system. The device is capable of producing a wide range of dosimetry, involving multiple modulations in both fixed and variable proton density dosimetry. Appropriately modulated multi-harmonic Radio Frequency (RF) signals in the lower end of the electromagnetic spectrum can be used in altering the cell signaling process using the TMP pathways, thus able to tackle systemic disorders. Generically known as Rotational Field Quantum Nuclear Magnetic Resonance (RFQMR), it is a technology that is made to deliver highly complex quantum instantaneous Nuclear Magnetic Resonance beams in the RF bands and its harmonics ranging from 3KHz to 300 MHz with a near field delivery using specialized antenna in the presence of high instantaneous magnetic field.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Male and female patients with clinically definite MS according to Polman
  • Age 18 to 60 yrs.
  • EDSS 0 to 7.
  • Relapse-free > 30 days prior to inclusion.
  • Stable immunomodulatory or immunosuppressive. therapy or treatment for > 3 months prior to inclusion.
  • In case of treatment with antidepressants:

stable therapy > 3 months prior to inclusion.

  • Highly effective methods of birth control for females.
Exclusion Criteria
  • Pregnancy
  • Cardiac pacemakers, biostimulators, neurostimulators, cochlear implants, hearing aids.
  • MRI incompatible implants like intramedullary nails, intracranial aneurysm clips, intra-orbital metal fragments, stents, implanted medication pumps etc near target area.
  • Critically ill patients needing life support system.
  • Mentally challenged patients who cannot give informed consent.
  • Severely ill patients who cannot lie in supine position for 1 hour.
  • H/o brain injury and/ or any malignant disorder
  • Personal or family history of epilepsy / brain tumor.
  • Relapse of MS < 30 days prior to inclusion
  • Change of immunomodulatory therapy < 30 days prior to inclusion
  • Bipolar disorder
  • History of stroke or other brain lesions

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
RFQMR on Multiple Sclerosis lesionsCytotron-
Primary Outcome Measures
NameTimeMethod
Effect of RFQMR therapy on MS lesion confirmed by Magnetic Resonance Imaging (MRI)Change from baseline to 90 days post therapy

1. Change in number of T1 gadolinium- enhancing lesions on MRI from baseline to 90 days post therapy.

2. Change in number of lesions on FLAIR MRI images from baseline to 90 days post therapy.

3. Change in volume of five larger lesions of brain and spine from baseline to 90 days post therapy

Secondary Outcome Measures
NameTimeMethod
Effect of RFQMR therapy on disability status and quality of life of MS patients.Change from baseline to 90 days post therapy

1. Change in Extended Disability Status Score (EDSS) from baseline to 90 days post therapy.

2. Change in Functional Assessment for Multiple sclerosis (FAMS) score from baseline to 90 days post therapy.

Trial Locations

Locations (1)

Centre for Advanced Research and Development

🇮🇳

Bangalore, Karnataka, India

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