Clinical trials in Delhi ncr
Manipal Hospitals, Delhi, conducts and participates in a broad spectrum of clinical research activities aligned with international standards of safety and oversight. The centre’s involvement in clinical trials in Delhi allows patients access to novel therapies under regulated conditions. This includes locally-led and global-collaboration studies within a hospital setting, offering robust ethical, regulatory, and monitoring frameworks. By engaging in such trials, the institution contributes to advances in medical knowledge, supports therapeutic innovation, and provides informed options for willing participants.
Hospital Locations
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Dwarka - Delhi NCR
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Gurugram - Delhi NCR
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Ghaziabad - Delhi NCR
How It Works
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Initial Screening: The process begins with preliminary eligibility screening based on inclusion and exclusion criteria to identify suitable participants for ongoing clinical trials.
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Informed Consent: Eligible patients are provided with detailed information about the study’s purpose, procedures, potential risks, and benefits before giving written informed consent.
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Eligibility Verification: Research clinicians conduct thorough evaluations, including medical history review, physical examination, and baseline laboratory or imaging investigations to confirm suitability for participation.
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Enrollment and Randomisation: Once qualified, participants are officially enrolled and, where applicable, randomly assigned to treatment or control groups according to the study protocol.
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Trial Intervention: Participants receive the designated investigational drug, medical device, or therapy under close clinical supervision to ensure safety and proper adherence.
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Ongoing Assessments: Regular follow-ups include safety checks, efficacy evaluations, and documentation of any side effects or adverse events by the research team.
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Regulatory Compliance: All trials are registered with the Clinical Trials Registry India (CTRI) and follow national and international ethical and regulatory standards.
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Data Management and Monitoring: The hospital’s research pharmacy, ethics committee, and monitoring systems ensure accurate data collection, patient protection, and transparent reporting of results.
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Request a CallbackBenefits
Choosing Manipal Hospitals for clinical trials ensures:
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Enables access to new treatments under well-controlled protocols for individuals in Delhi and surrounding regions.
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Aligns with ethical research practice, rigorous monitoring and regulatory registration for credible outcomes.
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Integrates multi-disciplinary teams, clinical investigators, research coordinators, and monitoring staff to manage the full trial lifecycle.
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Enhances knowledge of regional health needs and contributes to global medical evidence through locally conducted research.
What to Expect
Before Participation
The process begins with a comprehensive eligibility assessment, including review of medical history, diagnostic tests, and detailed discussions about the study’s goals and requirements. Once deemed suitable, participants go through an informed consent process where potential benefits, risks, and responsibilities are clearly explained. You are encouraged to ask questions and make an informed decision before enrollment.
During the Trial
After joining the study, participants undergo regular visits, clinical evaluations, and laboratory testing to monitor treatment safety, efficacy, and adherence to the research protocol. The research team maintains continuous supervision, addressing any side effects or concerns promptly. Collaborative communication between the treating physician, research coordinators, and support services ensures that your overall health and well-being remain the priority throughout the trial.
After the Trial
Upon study completion, participants may enter a follow-up or observation phase to assess long-term effects and ensure continued safety. Results and findings are documented transparently, and participants retain the right to withdraw or seek clarification at any stage. Manipal Hospitals ensures ethical oversight and patient care continuity before, during, and after the research process.
Why Manipal?
Manipal Hospitals offers a trusted and advanced platform for Delhi clinical trials, supported by robust hospital infrastructure and comprehensive research governance systems. The facility features dedicated research units, a fully functional institutional ethics committee, trained clinical research coordinators, and experienced monitoring teams that ensure protocol adherence and participant safety. Patients enrolling in clinical trials benefit from a hospital-based environment where patient safety, data accuracy, and regulatory compliance are of the highest priority.
The hospital’s multidisciplinary setup provides seamless access to specialist medical, diagnostic, and emergency services, ensuring complete care throughout all trial phases from recruitment and informed consent to follow-up. Each study conducted at Manipal Hospitals adheres strictly to national and international research standards, including registration with the Clinical Trials Registry – India (CTRI). The experienced research team ensures that every aspect of the study is guided by scientific integrity, transparency, and participant welfare.
Centre of Excellence
The Clinical Research Unit at Manipal Hospitals, Delhi, manages both investigator-initiated and industry-sponsored clinical studies with high standards of scientific and ethical compliance. Working closely with departments such as Medicine, Surgery, Oncology, and Paediatrics, the unit conducts clinical trials across diverse therapeutic areas, ensuring meticulous participant screening, monitoring, data documentation, and timely regulatory submissions.
Services Offered
The Clinical Research Unit at Manipal Hospitals, Delhi, provides end-to-end trial management through ethical, precise, and coordinated processes.
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Participant screening and enrolment
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Monitoring of study protocols and safety
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Research pharmacy and data management
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Ethics and regulatory oversight
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Post-trial follow-up and clinician coordination
Facilities & Services
Manipal Hospitals, Delhi, offers advanced infrastructure and support systems for safe, efficient Delhi clinical trials.
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Dedicated research suites and secure data systems
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Temperature-controlled pharmacy and storage
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On-site monitoring facilities
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Integrated specialist and diagnostic access
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Accredited labs and trained nursing staff
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Streamlined documentation and oversight processes
Frequently Asked Questions
A clinical trial is a structured study of an intervention in human participants to evaluate safety or effectiveness. At Manipal Hospitals, it involves screening, consent, intervention, monitoring and follow-up under regulated conditions.
Eligibility is determined by specific trial criteria. Patients meeting the required medical, demographic, and diagnostic parameters may be invited to participate in suitable clinical trials in Delhi at Manipal Hospitals.
Joining a trial may provide access to newer therapies, but it also carries uncertainties. The research team explains possible benefits, risks and how they are managed under the trial protocol.
Patient safety is prioritised through strict ethical reviews, CTRI registration, and continuous oversight by trained research staff. Regular safety assessments, adverse event reporting, and the right to withdraw at any stage ensure full protection and transparency.
After participation in clinical trials, you may enter follow-up care, transition to standard treatment or return to the treating clinician. The research unit provides closure details and recommendations.
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