A prospective, non-randomized, clinical study evaluating MR with volunteers

Not Applicable

Registration Number: CTRI/2020/06/025595

Lead Sponsor: Philips India Limited

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Open to Recruitment

Sex: Not specified

Target Recruitment: 0

Inclusion Criteria

1) Volunteeris willing and capable of providing informed consent and physically capable of performing study related activities.

2) Volunteer age between 18 -65 years old including either sex.

3) Volunteer has passed a general medical health check which involves laboratory investigations like CBC, ESR,RBS, Serum Creatinine, HIV, HbsAg, HCV, Urine analysis, ECG and UPT( for child bearing potential female subjects only).

Exclusion Criteria

1) Volunteers with any known contraindications for MR scanning

2) Volunteers with Pacemakers or other implanted electronic devices which are Non MR Compatible

3) Volunteers with metal implants which are not MR conditional or MR safe

4) Volunteers with small metal components in the body (vascular clips, metal splinters, stents, etc.) which are not MR conditional or MR safe

5) Volunteers with epilepsy

6) Volunteer with known severe cardiac disorders, Cerebrovascular, Respiratory, Hepatic, Renal, or Congenital anomaly or any other conditions as per the Physician opinion

7) Volunteers with uncontrolled hyper tension and diabetic Mellitus

8) Volunteers with dermal medicinal patches

9) Volunteers with mental illness or diseases, known claustrophobia, anxiety or panic disorders

10) Volunteers with Meniere’s disease or any previous history of tinnitis

11) Pregnant women

12) Volunteers with significant chronic illness

Study & Design

Study Type: Observational

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
There is no formal endpoint, as the study is not being conducted to test for safety and efficacy.Timepoint: There is no formal endpoint, as the study is not being conducted to test for safety and efficacy.

Secondary Outcome Measures

Name	Time	Method
There is no formal endpoint, as the study is not being conducted to test for safety and efficacy.Timepoint: There is no formal endpoint, as the study is not being conducted to test for safety and efficacy.