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

Primary Purpose

Multiple Sclerosis

Status
Unknown status
Phase
Phase 2
Locations
India
Study Type
Interventional
Intervention
Cytotron
Sponsored by
The Centre for Advanced Research & Development, India
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring Multiple sclerosis, RFQMR, Cytotron, EDSS, QOL assessment with FAMS

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Centre for Advanced Research and Development

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

RFQMR on Multiple Sclerosis lesions

Arm Description

Outcomes

Primary Outcome Measures

Effect of RFQMR therapy on MS lesion confirmed by Magnetic Resonance Imaging (MRI)
Change in number of T1 gadolinium- enhancing lesions on MRI from baseline to 90 days post therapy. Change in number of lesions on FLAIR MRI images from baseline to 90 days post therapy. Change in volume of five larger lesions of brain and spine from baseline to 90 days post therapy

Secondary Outcome Measures

Effect of RFQMR therapy on disability status and quality of life of MS patients.
Change in Extended Disability Status Score (EDSS) from baseline to 90 days post therapy. Change in Functional Assessment for Multiple sclerosis (FAMS) score from baseline to 90 days post therapy.

Full Information

First Posted
October 9, 2010
Last Updated
September 16, 2011
Sponsor
The Centre for Advanced Research & Development, India
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1. Study Identification

Unique Protocol Identification Number
NCT01220830
Brief Title
Cytotron® Delivered Rotational Field Quantum Nuclear Magnetic Resonance Therapy for Multiple Sclerosis
Acronym
RFQMR
Official Title
Efficacy of Rotational Field Quantum Nuclear Magnetic Resonance (RFQMR) Based Tissue Engineering in the Treatment of Multiple Sclerosis
Study Type
Interventional

2. Study Status

Record Verification Date
September 2011
Overall Recruitment Status
Unknown status
Study Start Date
September 2010 (undefined)
Primary Completion Date
December 2011 (Anticipated)
Study Completion Date
December 2011 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Centre for Advanced Research & Development, India

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Multiple sclerosis, RFQMR, Cytotron, EDSS, QOL assessment with FAMS

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
RFQMR on Multiple Sclerosis lesions
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Cytotron
Other Intervention Name(s)
CYTOTRON-RTE-6040-844GEN
Intervention Description
Exposure to RFQMR with Cytotron for 28 consecutive days for one hour daily.
Primary Outcome Measure Information:
Title
Effect of RFQMR therapy on MS lesion confirmed by Magnetic Resonance Imaging (MRI)
Description
Change in number of T1 gadolinium- enhancing lesions on MRI from baseline to 90 days post therapy. Change in number of lesions on FLAIR MRI images from baseline to 90 days post therapy. Change in volume of five larger lesions of brain and spine from baseline to 90 days post therapy
Time Frame
Change from baseline to 90 days post therapy
Secondary Outcome Measure Information:
Title
Effect of RFQMR therapy on disability status and quality of life of MS patients.
Description
Change in Extended Disability Status Score (EDSS) from baseline to 90 days post therapy. Change in Functional Assessment for Multiple sclerosis (FAMS) score from baseline to 90 days post therapy.
Time Frame
Change from baseline to 90 days post therapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ranjit Kumar, MD
Organizational Affiliation
SCALENE CYBERNETICS LIMITED
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre for Advanced Research and Development
City
Bangalore
State/Province
Karnataka
ZIP/Postal Code
560 049
Country
India

12. IPD Sharing Statement

Citations:
PubMed Identifier
5495918
Citation
Cone CD Jr. Variation of the transmembrane potential level as a basic mechanism of mitosis control. Oncology. 1970;24(6):438-70. doi: 10.1159/000224545. No abstract available.
Results Reference
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Cytotron® Delivered Rotational Field Quantum Nuclear Magnetic Resonance Therapy for Multiple Sclerosis

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