International Journal of Clinical Trials and Medical Research
Peer Reviewed · Open Access · Bi-monthly
DOI: 10.61148/IJCTMR
Current: Volume 1- Issue 6 - 2026
About the Journal
The International Journal of Clinical Trials and Medical Research (IJCTMR) is an international, peer-reviewed, open-access journal dedicated to publishing high-quality scientific research, clinical trial findings, systematic reviews, clinical studies, and innovative developments in clinical research.
The journal provides a platform for researchers, physicians, clinical investigators, healthcare professionals, and academicians to share scientific knowledge and advancements in clinical trials, human research, therapeutic interventions, clinical study design, and evidence-based medical practice.
IJCTMR aims to promote transparency, scientific excellence, research integrity, and the advancement of clinical research methodologies to improve healthcare outcomes worldwide.
Aims and Scope
The journal welcomes original research articles, clinical trial reports, systematic reviews, meta-analyses, research protocols, and other scholarly contributions covering the following areas:
- Clinical Trials and Clinical Research
- Randomized Controlled Trials
- Phase I, II, III and IV Clinical Trials
- Clinical Trial Design and Methodology
- Clinical Trial Management and Monitoring
- Clinical Research Ethics and Regulations
- Drug Development and Clinical Evaluation
- Investigational Medicinal Products
- Therapeutic Interventions and Outcomes
- Clinical Pharmacology and Drug Evaluation
- Evidence-Based Medicine
- Clinical Data Management and Biostatistics
- Clinical Trial Safety and Adverse Event Reporting
- Patient Recruitment and Retention
- Informed Consent and Research Participant Protection
- Multicenter and International Clinical Studies
- Real-World Evidence and Clinical Research
- Clinical Research Quality Assurance
- Research Protocol Development
- Clinical Trial Registration and Reporting
- Medical Device Clinical Investigations
- Translational and Experimental Clinical Research
Journal Objectives
The primary objectives of IJCTMR are to:
- Promote high-quality clinical trial research and medical investigations.
- Encourage ethical and transparent clinical research practices.
- Support innovation in clinical trial design and methodology.
- Disseminate reliable scientific findings from clinical studies.
- Encourage international collaboration among clinical researchers.
- Improve the quality, safety, and effectiveness of medical interventions.
- Advance evidence-based healthcare through clinical research.
Article Types
The journal considers the following manuscript categories:
- Original Research Articles
- Clinical Trial Reports
- Randomized Controlled Trial Studies
- Systematic Reviews and Meta-Analyses
- Clinical Research Protocols
- Review Articles
- Clinical Case Reports and Case Series
- Short Communications
- Research Methodology Articles
- Editorials
- Perspectives and Commentaries
- Clinical Research Guidelines
Open Access Policy
IJCTMR follows an open-access publishing model, providing readers worldwide with access to published research without subscription barriers. The journal supports the broad dissemination and exchange of scientific knowledge.
Peer Review Process
All submitted manuscripts undergo an initial editorial assessment to determine their suitability for the journal. Suitable manuscripts are considered for independent peer review by qualified experts in the relevant research fields.
Editorial decisions are based on originality, scientific quality, methodological rigor, ethical compliance, relevance, and research integrity.
Publication Ethics
Scholix Publishing is committed to maintaining high standards of publication ethics and research integrity.
Authors must comply with applicable clinical research regulations and ethical standards, including:
- Institutional Ethics Committee or IRB approval, where applicable.
- Informed consent from research participants.
- Clinical trial registration in an appropriate public registry before participant enrollment, where required.
- Transparent reporting of trial protocols and results.
- Disclosure of conflicts of interest and funding sources.
- Accurate reporting of adverse events and study limitations.
- Protection of participant privacy and confidentiality.
- Compliance with applicable research integrity and publication ethics guidelines.
Key Words
Clinical Trials, Clinical Research, Medical Research, Randomized Controlled Trials, Clinical Trial Design, Clinical Trial Management, Phase I Clinical Trials, Phase II Clinical Trials, Phase III Clinical Trials, Phase IV Clinical Trials, Clinical Study Protocols, Drug Development, Clinical Pharmacology, Therapeutic Interventions, Evidence-Based Medicine, Clinical Data Management, Biostatistics, Clinical Trial Monitoring, Research Ethics, Informed Consent, Patient Recruitment, Patient Safety, Adverse Event Reporting, Clinical Research Methodology, Multicenter Clinical Studies, Medical Device Trials, Real-World Evidence, Clinical Outcomes, Translational Research, Clinical Research Quality Assurance.
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