MRI scanning for design and development activities

Not Applicable

• Registration Number: CTRI/2018/07/014750
• Lead Sponsor: Philips India Limited

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Closed to Recruitment of Participants
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Participant is willing and able to give informed consent for participation in the study.

2. Participant is Healthy Male or Female, aged 18 years or above.

3. Participant has clinically acceptable laboratory

ECG

Chest X-ray

physical health (in the Investigators opinion) and willing to comply with all study requirements.

4. Volunteersâ?? Participant shall not have any condition that are contra-indicated for undergoing MRI Scanning.

5. Participant is willing to allow his or her general practitioner and consultant, if appropriate, to be notified of participation in the study.

Exclusion Criteria

The participant may not enter the study if ANY of the following apply:

1. Participant with any non-MR compatible implants or metallic foreign bodies, (Example: piercings, metal clips, surgical implants, pacemakers etc.)

2. Female participants who are pregnant, lactating or planning pregnancy during the course of the study.

3. Participants with significant renal, cardiac or hepatic impairment.

4. Participants with scheduled elective surgery or other procedures requiring general anesthesia during the study.

5. Participant who is terminally ill.

6. Participants who have participated in another research study involving an investigational product in the past 12 weeks.

7. Participants with Tattoos, permanent make up, Claustrophobia, anxiety or panic disorders, Epilepsy, and Meniereâ??s disease.

8. Participants with any other significant disease or disorder, which, in the opinion of the Investigator, may put the participants at risk because of participation in the study, or may influence the result of the study, or the participantâ??s ability to participate in the study.

9. Participants with any other condition as deemed unsuitable by the Medical Advisor.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
MRI System related adjustmentsTimepoint: 6 months

Secondary Outcome Measures

Name	Time	Method
Optimization of image quality and their preset settingsTimepoint: 6 months