Post Market Clinical Follow Up Investigation of Skanmobile and Skanmobile DR
Phase 4
Completed
- Conditions
- Health Condition 1: M955- Acquired deformity of pelvisHealth Condition 2: N219- Calculus of lower urinary tract, unspecifiedHealth Condition 3: M259- Joint disorder, unspecifiedHealth Condition 4: J709- Respiratory conditions due to unspecified external agent
- Registration Number
- CTRI/2020/09/028059
- Lead Sponsor
- Skanray Technologies Pvt Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Male and non pregnant female subjects of all age groups.
Subjects or legally authorised representatives or guardians on behalf of the subject who are able and willing to provide written informed consent to participate in this clinical investigation.
Exclusion Criteria
Pregnant or suspected to be pregnant based on the opinion of a physician.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Collection of feedback which includes investigator�s assessment of the overall safety and performance of the Skanmobile and Skanmobile DR found to be appropriate to meet the predefined objectives.Timepoint: Within 14 days after capturing the radiographic image
- Secondary Outcome Measures
Name Time Method Collection of feedback from the investigator on the radiographic images collected during the study and usability. This shall meet the predefined objectives to prove the claimed performance of Skanmobile and Skanmobile DR.Timepoint: Within 20 days after capturing the radiographic image.