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Study to see effectiveness of alternative cheaper solution used in patients undergoing a calcium removing procedure(rotational atherectomy) during angioplasty.

Not Applicable
Completed
Registration Number
CTRI/2021/01/030597
Lead Sponsor
il
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
48
Inclusion Criteria

1. Patients of either sex aged >18 years

2. Patients underwent percutaneous coronary intervention (PCI) with rotational atherectomy performed by operating physicians at Department of cardiology, KGMU Lucknow.

Exclusion Criteria

1. Patient with saphenous vein graft lesions

2. Patients with angiographic evidence of thrombus

3. Angiographic evidence of significant dissection at the treatment site

4. Patient with occlusions through which a guidewire could not be passed.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine the efficacy of alternative heparin based rota-flush solution without vasodilator, as compared to rota-flush solution containing vesodilator .Timepoint: At Baseline, at Discharge, and after 4 weeks.
Secondary Outcome Measures
NameTimeMethod
To determine the safety of alternative heparin based rota-flush solution without vasodilator, as compared to rota-flush solution containing vesodilator .Timepoint: 1 month
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