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CTRI Number  CTRI/2025/11/097678 [Registered on: 18/11/2025] Trial Registered Prospectively
Last Modified On: 18/11/2025
Post Graduate Thesis  No 
Type of Trial  Interventional 
Type of Study   Medical Device 
Study Design  Randomized, Parallel Group Trial 
Public Title of Study   A Multicenter Study Comparing Devices for Treating Severe Calcium Buildup in Heart Arteries 
Scientific Title of Study   A Prospective, Multicenter, Randomized Study Comparing Orbital Atherectomy to Other Calcium Modification Strategies in Patients with Severely Calcified Coronary Lesions 
Trial Acronym  ORBIT-CALM Study 
Secondary IDs if Any  
Secondary ID  Identifier 
ORBIT-CALM Study/2025  Protocol Number 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  Dr Prathap Kumar N 
Designation  Chief Interventional Cardiologist 
Affiliation  Meditrina Hospitals Pvt Ltd 
Address  Ayathil, Kottamkara, Kollam, Kerala

Kollam
KERALA
691021
India 
Phone  7025222244  
Fax    
Email  prathapndr@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  Dr Prathap Kumar N 
Designation  Chief Interventional Cardiologist 
Affiliation  Meditrina Hospitals Pvt Ltd 
Address  Ayathil, Kottamkara, Kollam, Kerala


KERALA
691021
India 
Phone  7025222244  
Fax    
Email  prathapndr@gmail.com  
 
Details of Contact Person
Public Query
 
Name  Dr Prathap Kumar N 
Designation  Chief Interventional Cardiologist 
Affiliation  Meditrina Hospitals Pvt Ltd 
Address  Ayathil, Kottamkara, Kollam, Kerala


KERALA
691021
India 
Phone  7025222244  
Fax    
Email  prathapndr@gmail.com  
 
Source of Monetary or Material Support  
ABBOTT HEALTHCARE PVT LTD. Office Floor, The Suryaa Hotel. New Friends Colony. New Delhi 110 025 India 
 
Primary Sponsor  
Name  Interventional Cardiology Research and Training Foundation 
Address  31/2487/86, Near Meditrina Hospital, Ayathil P.O, Ayathil, Kollam, Kerala, India, 691021 
Type of Sponsor  Other [Research & Training Foundation] 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 7  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Tom Devasia  Kasturba Medical College and Hospital  Department of Cardiology, OPD Block, Kasturba Medical College and Hospital, MAHE, Manipal - 576104, Karnataka, India
Uttara Kannada
KARNATAKA 
9448158508

tom.devasia@manipal.edu 
Dr Girish Godbole  KIMS Hospital  Survey No. 37 & 38, PES University EC Campus, Hosur Rd, Konappana Agrahara, Electronic City, Bengaluru, Karnataka 560100
Bangalore
KARNATAKA 
9845866395

drgirish1@gmail.com 
Dr Dilip Kumar  Manipal Hospital  E.M. Bypass, 127, Mukundapur, E.M. Bypass, Kolkata 700099, West Bengal, India
Kolkata
WEST BENGAL 
9748487563

dilipcardio@gmail.com 
Dr Prathap Kumar N  Meditrina Hospital  Department of Cardiology, Ayathil, Kottamkara, Kollam, Kerala 691021
Kollam
KERALA 
70252 22244

prathapndr@gmail.com 
Dr Arun Gopi  Metromed International Cardiac Centre  Department of Cardiology, Metromed International Cardiac Centre, Thondayad, Bypass Road, opposite Mahindra Trucks And Bus, Palazhi, Kozhikode, Kerala 673014
Kozhikode
KERALA 
8157047371

arungopi@gmail.com 
Dr Asish kumar Mandalay  myHart Hospital  myHart Hospital, Thondayad, Kozhikode, Kerala 673017
Kozhikode
KERALA 
9895443390

asishmandalay@gmail.com 
Dr Ramesh Gadepalli  Yashodha Hospital  Departnent of Cardiology IId Floor, OP No: ll, Yashoda Hospitals Yashoda Healthcare Services Pvt. Ltd SP Road, Secunderabad, Telangana - 500003
Hyderabad
TELANGANA 
9394699297

rgadepalli@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 7  
Name of Committee  Approval Status 
Clinical Research Ethics Committee  Submittted/Under Review 
CLINICOM  Submittted/Under Review 
Diabcare India  Submittted/Under Review 
Instituitional Ethics Committee Metromed International Cardiac Centre  Submittted/Under Review 
KMC and KH Institutional Ethics Committee  Submittted/Under Review 
Meditrina Ethics Committee  Approved 
Yashoda Academy of Medical Education And Research  Submittted/Under Review 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: I25||Chronic ischemic heart disease, (2) ICD-10 Condition: I214||Non-ST elevation (NSTEMI) myocardial infarction, (3) ICD-10 Condition: I200||Unstable angina,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Intervention  Orbital Atherectomy  Orbital Atherectomy is a calcium-modifying device routinely used prior to Percutaneous Coronary Intervention (PCI) to modify calcified plaques and facilitate stent deployment. Duration - The device is used only once during the procedure. 
Comparator Agent  Rotational atherectomy, Intravascular Lithotripsy, cutting and scoring ballon  Rotational Atherectomy, Intravascular Lithotripsy (IVL), and cutting and scoring balloons are calcium-modifying devices routinely used prior to Percutaneous Coronary Intervention (PCI) to modify calcified plaques and facilitate successful stent deployment. Duration: These devices either alone or in combination will be used only once during the procedure. 
 
Inclusion Criteria  
Age From  18.00 Year(s)
Age To  90.00 Year(s)
Gender  Both 
Details  1. Patients of either gender, aged 18 years and above
2. Patients presenting with any one of the following conditions (a) stable ischemic heart disease, (b) acute coronary syndrome (NSTEMI or unstable angina)
3. Patients willing to sign written informed consent

Imaging Inclusion Criteria
1. Use of OCT guidance is mandatory for all enrolled patients
2. Patients presenting with balloon crossable lesion
3. The target lesion(s) is a de novo coronary lesion with stenosis more than equal to 50% and less than 100%, the reference diameter of each target vessel is more than equal to 2.5 mm and less than 4.0 mm at the lesion site.
4. The target lesion has OCT evidence of severe calcium at the lesion site. 
 
ExclusionCriteria 
Details  1. Patients presenting with non-balloon crossable lesion
2. Patients with a history of coronary artery bypass grafting
3. Patients with hemodynamic instability or cardiogenic shock
4. Patients with chronic total occlusion and In-stent restenosis lesions
5. Patients with contraindication for dual antiplatelet therapy (DAPT)
6. Patients with recent STEMI
7. Patients unwilling to sign the informed consent

Angiographic Exclusion criteria
1. The target lesion is located within a bypass graft
2. Angiographic evidence of thrombus
3. Angiographic evidence of significant dissection at the treatment site 
 
Method of Generating Random Sequence   Stratified block randomization 
Method of Concealment   An Open list of random numbers 
Blinding/Masking   Not Applicable 
Primary Outcome  
Outcome  TimePoints 
Rate of technical success between the two treatment arms   Baseline (Post-Procedure) 
 
Secondary Outcome  
Outcome  TimePoints 
1. MACE
2. Optimal Stent expansion
3. Cost Effectiveness
4. Clinical Success 
1. In-hospital & 30 days
2. Post-Procedure
3. 30 days
4. Post-Procedure 
 
Target Sample Size   Total Sample Size="164"
Sample Size from India="164" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   N/A 
Date of First Enrollment (India)   30/11/2025 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="1"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)   Not Applicable 
Recruitment Status of Trial (India)  Not Yet Recruiting 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

Coronary artery disease (CAD), also known as ischemic heart disease, is the leading cause of mortality worldwide, contributing to 108 deaths per 100,000 people and 2,275.9 disability-adjusted life years (DALYs) per 100,000. The World Health Organization reports that cardiovascular diseases account for 17.9 million deaths annually.  In India, the prevalence of CAD is approximately 10.5%, higher than the global average of 8.8%. The increasing burden of CAD, driven by risk factors such as diabetes, hypertension, dyslipidemia, and smoking, has led to a growing need for revascularization procedures, particularly percutaneous coronary intervention (PCI).

Percutaneous coronary intervention (PCI) has significantly advanced the management of CAD by restoring coronary blood flow. However, the higher prevalence of coronary artery calcification (CAC) in PCI patients complicates this procedure. Severe CAC, present in 5.9% to 20% of PCI patients, obstructs stent delivery and deployment, hindering optimal stent expansion and increasing the risks of early complications such as vessel closure, slow flow, dissection, perforation, stent dislodgement, and embolization, as well as late complications like stent thrombosis, in-stent restenosis, and aneurysm formation. To address these challenges, advanced plaque-modification strategies, such as orbital atherectomy (OA), rotational atherectomy (RA), intravascular lithotripsy (IVL), and cutting or scoring balloons, are employed based on lesion characteristics, the patient’s clinical condition, and the operator’s expertise.

The Diamondback 360® Coronary Orbital Atherectomy System (OAS) by Cardiovascular Systems Inc., approved by the US Food and Drug Administration (FDA) in late 2013, represents a significant advancement in the treatment of severely calcified coronary artery lesions. Specifically indicated for de novo, severe CAC, OA is the only FDA-approved device designed to improve stent delivery by addressing heavily calcified lesions. This innovative technology utilizes a bi-directional burr passage and elliptical propagation, which reduces the risk of burr entrapment, making it an essential tool for interventional cardiologists. Recognized for its efficacy in preparing coronary lesions for PCI, OA has become critical in managing complex CAD with severe calcifications. The 2021 ACC/AHA/SCAI guidelines further endorse the use of OA to improve procedural success and optimize patient outcomes in these challenging cases.

Despite its growing use, the comparative effectiveness of OA versus other calcium modification techniques has not been sufficiently evaluated in large-scale studies. This prospective, multicenter, randomized study aims to compare the clinical, technical, and economic outcomes of OA with other calcium-modifying devices in patients with severely calcified coronary lesions. The study will address the need for evidence-based guidelines for managing these high-risk lesions and provide insights into the cost-effectiveness of OA compared to other strategies.

 
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