Clinical Trials Programme
Iswarya Hospital conducts clinical trials in collaboration with leading research institutions and pharmaceutical companies, offering patients access to cutting-edge treatments and contributing to the advancement of medical science.
What Are Clinical Trials?
Clinical trials are carefully designed research studies that test new treatments, medications, or medical devices in human volunteers. They are the primary pathway through which new therapies move from the laboratory to the patient.
By participating in a clinical trial, you may gain early access to promising new treatments while contributing to medical knowledge that benefits future patients worldwide.
Phase I
Tests safety and dosage in a small group of 20-80 volunteers
Phase II
Evaluates effectiveness and side effects in 100-300 patients
Phase III
Confirms benefits in large groups of 1,000-3,000 patients
Phase IV
Post-market surveillance for long-term safety monitoring
Active Trial Areas
Specialties conducting clinical research at Iswarya Hospital
Oncology
Immunotherapy, targeted therapy, CAR T-Cell therapy, and novel chemotherapy combinations for solid tumours and blood cancers.
Cardiology
New anticoagulants, heart failure medications, cardiac device trials, and interventional cardiology techniques.
Nephrology
Novel dialysis modalities, transplant immunosuppression optimisation, and chronic kidney disease management.
Neurology
Stroke prevention medications, epilepsy treatment innovations, and neurodegenerative disease therapies.
Patient Safety & Your Rights
Your wellbeing is our top priority
Informed Consent
You will receive a detailed explanation of the trial, its risks, benefits, and alternatives before agreeing to participate.
Ethics Committee Oversight
Every trial is reviewed and approved by our Institutional Ethics Committee (IEC) before any patient is enrolled.
Data Privacy
Your personal and medical data is kept strictly confidential, de-identified, and stored securely.
Right to Withdraw
You can withdraw from any trial at any time, for any reason, without affecting your ongoing medical care.
GCP Compliance
All trials follow Good Clinical Practice (GCP) guidelines set by CDSCO and international regulatory bodies.
Medical Monitoring
Regular health check-ups and monitoring throughout the trial to ensure your safety at every stage.
How to Participate
5 steps from enquiry to enrolment
Enquiry
Contact us or ask your treating doctor about available trials for your condition.
Eligibility Screening
Our research team reviews your medical history to determine if you qualify.
Informed Consent
You receive detailed information and sign consent only if you wish to proceed.
Treatment & Monitoring
You receive the trial treatment with regular health monitoring and follow-ups.
Follow-Up
Continued monitoring after the trial to track long-term outcomes and safety.
Regulatory Compliance
All clinical trials at Iswarya Hospital comply with regulations set by the Central Drugs Standard Control Organisation (CDSCO), Indian Council of Medical Research (ICMR), and international Good Clinical Practice (ICH-GCP) guidelines. Trials are registered with the Clinical Trials Registry of India (CTRI).
Frequently Asked Questions
Are clinical trials safe?▼
Yes. Every trial undergoes rigorous review by our Ethics Committee and follows international safety standards. Your health is monitored throughout the trial.
Will I receive a placebo instead of real treatment?▼
Some trials use placebos, but this is always disclosed during the informed consent process. Many trials compare a new treatment against the current best treatment, not a placebo.
Is there any cost to participate?▼
In most clinical trials, the study medication, related tests, and monitoring are provided free of charge. You will be informed of any costs during the consent process.
Can I withdraw from a clinical trial?▼
Absolutely. You can withdraw at any time without giving a reason. Your regular medical care at Iswarya Hospital will not be affected in any way.
How is my personal data protected?▼
Your data is de-identified (coded), stored securely, and shared only with authorised researchers. We comply with Indian IT Act provisions and ICMR data protection guidelines.
Who approves clinical trials at Iswarya Hospital?▼
Our Institutional Ethics Committee (IEC), comprising medical experts, legal advisors, and community representatives, reviews and approves every trial before it begins.
Interested in Participating?
Whether you are a patient interested in trial participation or a pharmaceutical company seeking a clinical trial partner, contact our Research Department.