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Ultrasound Studyâ?? Reliance Diagnostic

Philips Ultrasound Study Protocol â?? Reliance Diagnostic

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/11/047315
Enrollment
200
Registered
2022-11-15
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

None listed

Sponsors

Philips Ultrasound, Inc.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subject (or legal representative where appropriate) is willing and capable of providing informed consent and physically capable of performing study related activities. 2. Subject is indicated for a routine ultrasound exam at the site, including with or without examination with contrast.

Exclusion criteria

Exclusion criteria: 1. Subjects with any known contraindications for ultrasound scanning. 2. Philips employees and their family members. 3. Subjects under 18 years of age

Design outcomes

Primary

MeasureTime frame
The feedback obtained during the study will be used to guide product optimization and development. No statistical analysis will be conducted, as the study evaluates user preference. Data may be collected to validate user needs for final product designs.Timepoint: 1 day

Secondary

MeasureTime frame
Not ApplicableTimepoint: Not Applicable

Countries

India

Contacts

Public ContactMr Hasan Ali Ahmed

Reliance Diagnostic

tanuj1967@gmail.com9837072571

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026