Genetics Study of In-stent Restenosis

NCT ID: NCT01670396

Last Updated: 2012-08-22

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-03-31

Study Completion Date

2012-09-30

Brief Summary

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The investigators hypothesized that genetic variants of G protein influence the development of restenosis and clinical outcome of patients receiving drug-eluting stents (DES).

Detailed Description

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Although drug-eluting stents (DES) have reduced restenosis rates compared with bare-metal stents, the restenosis rate is still high in the high-risk group. G protein plays important roles in the signal transduction leading to vascular smooth muscle proliferation. The initial and subsequent studies suggest that the T allele of C825T polymorphism is associated with enhanced transmembrane signaling via Gi proteins.

Conditions

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Coronary Artery Disease

Keywords

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coronary stent implant polymorphism G protein drug-eluting stent restenosis

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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in-stent restenosis

No interventions assigned to this group

non-in-stent restenosis

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Patients who underwent follow-up angiography. All the patients must had been implanted with DES during the last two years.

Exclusion Criteria

* For the non-ISR group, the patients underwent follow-up angiography less than 6 months away from stent implanting.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Shanghai Zhongshan Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Zhongshan Hospital

Shanghai, , China

Site Status RECRUITING

Countries

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China

Central Contacts

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Yamei Xu

Role: CONTACT

Phone: 8613917133371

Email: [email protected]

Facility Contacts

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Yamei Xu

Role: primary

Other Identifiers

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ZS-XN-ISR

Identifier Type: -

Identifier Source: org_study_id