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CompletedNCT01551875Score-IndiaUpdated Jul 9, 2013

A Study to Derive Normative Distribution of CIMT and to Determine Its Correlation With Cardiovascular Risk Factors

An observational study in Carotid Intima- Media Thickness, sponsored by AstraZeneca. Completed at 24 sites in India. Open to participants aged 30 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-07-09.

Sponsored by AstraZeneca · Observational

Study type
Observational
Time perspective
Prospective
Enrollment
1,200
Ages
30 Years and older
Sex
All
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Study summary

This non-interventional, prospective, multi-centric, cross-sectional study is aimed to obtain the distribution of measurements of CIMT in Indian subjects and will involve approx. 30 investigative sites from all over the country. Each investigative site will be expected to enrol 50 subjects and Carotid intima-media thickness (CIMT) values will be taken for each individual as described in the protocol.

All the procedures could be completed in a single day, however due to any reason any study variable is not taken subject may be asked to come back for a second visit within 7 days of the first visit.

Read the detailed description

A Study to derive normative distribution of CIMT and to determine its cOrrelation with cardiovascular Risk factors in asymptomatic nationwidE Indian population. (SCORE India)

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Conditions studied

  • Carotid Intima- Media Thickness

Keywords

  • CIMT
  • cardiovascular disease
  • correlation with cardiovascular Risk factors
03

In context

Lead sponsor

AstraZeneca is the lead sponsor of 3,429 studies on the registry; 270 are open to participants now.

Of its 357 completed or terminated interventional studies of FDA-regulated products, 173 (48%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
30 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Asymptomatic subjects with or without risk factors but not suffering from any established cardiovascular event.

Inclusion criteria

  • Provision of subject informed consent
  • Female or male aged 30 years and over

Exclusion criteria

Exclusion Criteria:

  • Subjects with established cardiovascular event
  • Intake of lipid lowering drug in the past 3 month
  • Subjects with known hypersensitivity to carotid bulb
  • Pregnant or lactating women
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Study design

Time perspective
Prospective
Enrollment
1,200 participants (actual)

Groups and cohorts

  • subjects who are meeting the inclusion criteria
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What researchers measure

Primary outcomes

  1. CIMT values in centimeters (unit) of male and female subjects without established cardiovascular disease.

    Time frame: at visit 1

07

Study locations

24 sites
  • Research Site
    Ahmedabad, Gujarat, India
  • Research Site
    Vadodara, Gujarat, India
  • Research Site
    Gurgaon, Haryana, India
  • Research Site
    Keshwapur, Hubli, India
  • Research Site
    Nampally, Hyderabad, India
  • Research Site
    Punjab, Jalanhar, India
  • Research Site
    Bangalore, Karnataka, India
  • Research Site
    Mangalore, Karnataka, India
  • Research Site
    Mumbai, Maharashtra, India
  • Research Site
    Nerul, Navi Mumbai, India
  • Research Site
    Delhi, New Delhi, India
  • Research Site
    Dhanvantri Nagar, Pondicherry, India
  • Research Site
    Jipur, Rajasthan, India
  • Research Site
    Chennai, Tamil Nadu, India
  • Research Site
    Poonkunnam, Thrisur, India
  • Research Site
    Pattom, Trivandum, India
  • Research Site
    Noida, UP, India
  • Research Site
    Varanasi, UP, India
  • Research Site
    Ghaziabad, Uttar Pradesh, India
  • Research Site
    Kolkata, West Bengal, India
  • Research Site
    Chandigarh, India
  • Research Site
    Indore, India
  • Research Site
    Lucknow, India
  • Research Site
    Pune, India
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 9, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01551875
Lead sponsor
AstraZeneca
Responsible party
Sponsor
First posted
Mar 13, 2012
Start date
May 2012
Primary completion
Jul 2013
Completion
Jul 2013
Last update
Jul 9, 2013

Study contacts

Paurus M Irani, MD
study director · AstraZeneca Pharma India Ltd.
R R Kasliwal, DM
principal investigator · Medanta, The Medicity, Gurgaon

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2013. You cannot join it, but the record below documents what was studied.

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