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Notification & Updates

  • list icon Health Condition of trial participants is now coded as per ICD-10 classification and must be chosen from the drop down list.
  • list icon Health Condition of trial participants is now coded as per ICD-10 classification and must be chosen from the drop down list.
  • list icon Health Condition of trial participants is now coded as per ICD-10 classification and must be chosen from the drop down list.
  • list icon Health Condition of trial participants is now coded as per ICD-10 classification and must be chosen from the drop down list.
  • list icon Health Condition of trial participants is now coded as per ICD-10 classification and must be chosen from the drop down list.
  • list icon Health Condition of trial participants is now coded as per ICD-10 classification and must be chosen from the drop down list.

Keyword Search

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Nation-Wise Analytics

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Active Clinical Trials Across States

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Total Registered Trials (All Phases)

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Research Publications Linked to Registered Trials

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Institution-Wise Trial Contributions

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Participant Recruitment Status by Region

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Trial Categories & Therapeutic Area Distribution

India’s clinical research ecosystem is expanding rapidly, supported by diverse patient populations, advanced institutions, and a strong regulatory framework that ensures ethical and transparent trial practices. Each state across the country contributes uniquely to this landscape, reflecting regional healthcare needs, disease patterns, and institutional capabilities.

Resources & Policies

New Applicant Registration Tutorial
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New Applicant Registration Tutorial

11 minutes 22 seconds

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New Applicant Registration Tutorial
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New Applicant Registration Tutorial

11 minutes 22 seconds

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Clear Guidelines for Accurate and Compliant Trial Registration

Our Standard Operating Procedures provide step-by-step instructions to ensure all clinical trial submissions are consistent, complete, and aligned with national regulatory standards. These guidelines help researchers understand required documentation, data entry formats, ethical approvals, and update protocols. By following the SOPs, institutions can reduce errors, streamline the registration process.

Download the SOP Document Below

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    SOP Document

    20 Pages

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Declaration of Responsibility and
Compliance with Prospective CTRI
Registration

The information provided on the Clinical Trials Registry – India (CTRI) platform is submitted by researchers, sponsors, and authorized institutions conducting clinical trials across the country. While every effort is made to review and ensure the accuracy and completeness of submitted data.

Download the Disclaimer Document Below

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    Disclaimer Document

    20 Pages

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About Clinical Trial Registry India

Clinical trials hold enormous potential for benefiting patients, improving therapeutic regimens and ensuring advancement in medical practice that is evidence based. Unfortunately, the data and reports of various trials are often difficult to find and in some cases do not even exist as many trials abandoned or are not published due to "negative" or equivocal results. However, this tendency for availability of only selective information from the myriad clinical trials conducted is not commensurate with the practice of "evidence-based medicine". Today, world over, a need has been felt on the imperative for transparency, accountability and accessibility in order to re-establish public trust in clinical trial data.

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mission Mission

The mission of the Clinical Trials Registry-India (CTRI) is to ensure that all clinical trials conducted in India are prospectively registered, i.e. before the enrolment of the first participant. Additionally, post-marketing surveillance studies.

vision Vision

The vision of the CTRI is to ensure that every clinical trial conducted in the region is prospectively registered with full disclosure of the trial data set items. While this register is meant primarily for trials conducted in India, the CTRI will also accept registration of trials

How It Works

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Trial Registration by Researchers

Researchers begin by submitting key details of their clinical trial, including objectives, methodology, eligibility criteria

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Review, Verification & Quality Check

After submission, the CTRI team reviews the information for accuracy, completeness, and compliance with ethical guidelines.

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Public Disclosure on the CTRI Portal

Once verified, the trial is published on the CTRI platform, making essential information—such as purpose, design, recruitment needs, and contact details

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Continuous Updates Throughout the Study Lifecycle

Researchers must keep their trial records updated with progress reports, recruitment status, amendments, and final results.

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CTRI GALLERY

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CTRI GALLERY

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CTRI GALLERY

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CTRI GALLERY

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CTRI GALLERY

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CTRI GALLERY

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CTRI GALLERY

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CTRI GALLERY

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CTRI GALLERY

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FAQ’s

Yes. All trial submissions undergo a review process to ensure completeness, accuracy, and compliance with ethical standards. Researchers may be asked to revise details if any discrepancies are found.
Yes. All trial submissions undergo a review process to ensure completeness, accuracy, and compliance with ethical standards. Researchers may be asked to revise details if any discrepancies are found.
Yes. All trial submissions undergo a review process to ensure completeness, accuracy, and compliance with ethical standards. Researchers may be asked to revise details if any discrepancies are found.
Yes. All trial submissions undergo a review process to ensure completeness, accuracy, and compliance with ethical standards. Researchers may be asked to revise details if any discrepancies are found.
Declaration of Responsibility and Compliance with Prospective CTRI Registration

I/we (Student and Guide/Overall Trial Coordinator (PI)/Co-PI/Site-PI/Sponsor/Ethics Committee/CRO) hereby declare and affirm that:

  • No participant has been enrolled in the clinical trial prior to registration with the Clinical Trials Registry - India (CTRI).
  • The Ethics Committee approval submitted is valid, has been obtained within the last one year, and the entire duration of the proposed clinical trial is within the validity period of this approval.
  • We accept joint and full responsibility for ensuring prospective CTRI registration, and for the accuracy, authenticity, and completeness of all information and documentation submitted.

We fully understand that any instance of:

  • False or misleading declaration
  • Use of forged or expired Ethics Committee or DCGI regulatory documents
  • Retrospective registration of the trial
  • Misrepresentation of trial-related information

shall constitute a serious breach of CDSCO/DHR/ICMR/WHO guidelines and institutional policies.

In the event of such non-compliance, we acknowledge and accept that we may be held individually and collectively liable and may be subject to disciplinary action, academic sanctions, withdrawal of Ethics Committee clearance, or legal proceedings as deemed appropriate by the University, Ethics Committee, regulatory authorities, or any competent body.

CTRI relies solely on the information submitted by investigators, sponsors, and institutions. It assumes no responsibility for the verification of the authenticity of documents.

Any clinical trial found to be retrospectively registered, based on invalid or falsified documentation, or conducted beyond the approved duration will be flagged accordingly and may be reported to the appropriate authorities and will lead to freezing of registrants account in CTRI.