Clinical Trials Policy
IJMSCRR follows international best practices for the ethical conduct and transparent reporting of clinical research.
1. Registration Requirement
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All clinical trials must be registered in a publicly accessible database prior to the start of patient enrollment.
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Acceptable registries include:
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Other nationally or internationally recognized registries.
2. Mandatory Disclosure
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The registration number and name of the registry must be included in the manuscript (preferably in the Methods section).
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Manuscripts describing unregistered trials may be rejected without review.
3. Ethical Standards
- All studies involving human participants were conducted in accordance with the ethical principles of the Declaration of Helsinki. The study protocol was reviewed and approved by the relevant Institutional Review Board (IRB) or Ethics Committee where applicable. This journal adheres to the ethical guidelines for medical research involving human subjects as outlined in the Declaration of Helsinki. The full guideline is available at: https://www.wma.net/what-we-do/medical-ethics/declaration-of-helsinki/
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Informed consent must be obtained from all participants.