| 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
|
|
|
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
|
|
|
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. |