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Clinical Research

    Sailing ship from the 18th century to depict the type of vessel for randomized clinical trial history
    Life-Science EventsPatient Recruitment and Retention

    Celebrating Clinical Trials Day: From a Shipboard Study Site to Today

    by William McEwen May 20, 2026
    written by William McEwen

    Quick Summary

    James Lind’s 18th-century shipboard experiment is a landmark moment in the history of clinical research, demonstrating how controlled comparisons can reveal effective treatments. We reimagined his study with a modern protocol title and criteria, then connected his work to the professionals who advance research today.

    ______________________________________________________

    The Surprising Origin of Randomized Controlled Clinical Trials

    Clinical trials reach back much further than many people expect. On May 20, 1747, a Scottish surgeon named James Lind began a monumental experiment aboard a British Royal Navy ship. Lind’s work is a key moment in the history of clinical research, and his experiment is widely considered the first controlled randomized clinical trial in modern times.

    In the 18th century, scurvy was a serious health threat for sailors at sea. Lind divided 12 sailors suffering from scurvy into six pairs. He provided each pair with a different dietary supplement to observe which ones improved their symptoms.

    Lind carefully controlled the conditions so that all participants remained in similar circumstances. He chose men with similar symptoms, kept them in the same place, and gave them a common diet. Lind observed that the pair who received oranges and lemons improved far more than the others.

    Image of citrus fruit used to prevent scurvy in clinical trial historyLind’s experiment demonstrated that citrus fruits were the most effective treatment among the options he tested for preventing scurvy. And while his experiment is significant in the history of clinical research and his conclusions proved correct, his findings were not implemented for more than 40 years. Once citrus became a required part of sailors’ diets, serious cases of scurvy largely disappeared.

    It’s interesting to note that there were clues that citrus was the answer to scurvy long before Lind got involved. But it took Lind, his experiment, and another 40 years before the benefits were put to use.

    History of Clinical Research Reimagined

    Just for fun, I wrote a modern-day protocol title for Lind’s experiment:

    A Prospective, Randomized, Controlled, Parallel Group Study Evaluating the Effect of Citrus and Other Dietary Interventions on Scurvy Symptoms in Royal Navy Sailors

     And I didn’t stop there. Here is a modern version of Lind’s inclusion-exclusion criteria:

    Inclusion Criteria

    • Active-duty Royal Navy sailor
    • Current signs and symptoms consistent with scurvy
    • Similar severity of illness at enrollment
    • Residing aboard the same ship during the study period
    • Willing and able to follow the assigned dietary intervention

     Exclusion Criteria

    • No clear signs of scurvy
    • Advanced illness requiring care outside the study conditions
    • Inability to remain on the common shipboard diet
    • Inability to complete the observation period
    • Any condition that would make the response to the dietary intervention difficult to assess
    • An immediate family member, such as a spouse, parent, sibling, or child of Dr. Lind or a member of Dr. Lind’s study team

    Celebrating Clinical Trials Today

    Lind’s trial helped lay the foundation for modern clinical research and evidence-based practice. International Clinical Trials Day was launched on May 20, 2005, to commemorate Lind’s pioneering contribution and to honor clinical research professionals each year.

    Imperial sends a special thank you to our research partners and to research professionals everywhere. We celebrate your work in discovering safe and effective treatments and in developing better ways to detect, diagnose, and reduce the risk of disease.

    Thank you!

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    May 20, 2026 0 comment
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  • Ancillary Trial Supplies and EquipmentLife-Science Events

    Why Ancillary Supplies Are Becoming a Critical Part of Clinical Trial Planning

    by Dan McDonald May 19, 2026
    by Dan McDonald May 19, 2026

    Quick Summary Ancillary supplies have always been part of clinical trial planning, but they haven’t always received the level of attention they deserve. Increasingly, sponsors, CROs, and clinical supply teams are recognizing how much non‑drug materials, everything from equipment to kitted supplies, can influence timelines,…

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  • Clinical Trial Writing and Design

    Writing Clinical Study Materials: Why Starting Early Can Be an Option

    by Liz Wegner May 6, 2026
    by Liz Wegner May 6, 2026

    Clinical studies follow established timelines, and the work of preparing site and participant materials typically begins at a predictable point in that process. Most study teams assume writing begins only after the protocol is approved, and often don’t consider alternatives. Naturally, the best time to…

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  • Clinical Trial Writing and DesignPatient EngagementPatient Recruitment and Retention

    The Reader Experience: Making Clinical Research Participant Materials Easy to Use

    by William McEwen April 22, 2026
    by William McEwen April 22, 2026

    Much of life is rooted in communication, and this is certainly true in clinical research. Every study interaction, whether in person or through participant clinical trial materials, depends on clear and reliable information. When we communicate with participants, we convey essential details and set expectations.…

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  • Business Insights

    Risk Management in Clinical Trials Through Effective CAPA Practice

    by Frances Bentley April 8, 2026
    by Frances Bentley April 8, 2026

    Risk management in clinical trials depends on systems that detect issues, correct them, and prevent them from returning. Corrective and Preventive Actions (CAPAs) are the structured process used to investigate deviations, address root causes, and strengthen controls. When CAPAs work, they protect study integrity and…

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  • Business Insights

    Sustainability in Action: ESG and Clinical Research

    by Dan McDonald March 16, 2026
    by Dan McDonald March 16, 2026

    Sustainability has become a top priority for businesses and now shapes how they are evaluated and trusted. Companies in every industry are judged not only on their results and profits, but also on how they operate. In life sciences, using sustainable practices in clinical trials…

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  • Life-Science EventsPatient EngagementStudy Site Management

    Harnessing Collective Intelligence in Clinical Trials

    by Hope Cullen March 10, 2026
    by Hope Cullen March 10, 2026

    Clinical studies are complex, and they work better when the people involved share what they know. That may sound obvious, but sponsors, CROs, sites, technology partners, and patients often end up working in separate corners. This makes it harder for important information to move where…

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  • Clinical Trial Writing and DesignPatient EngagementPatient Recruitment and RetentionSite Materials & Logistics

    White Space is Not a Missed Opportunity in Clinical Study Materials

    by William McEwen March 3, 2026
    by William McEwen March 3, 2026

    Discover how print and digital clinical study materials, developed with clarity, white space, and purpose, improve participant understanding and engagement. White space refers to the empty area around print and design text and graphic elements. Long ago, in a different industry, I was part of…

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  • Ancillary Trial Supplies and EquipmentBusiness InsightsPatient Engagement

    Wearables & AI in Clinical Trials: Balancing Innovation & Integrity

    by Ted Corrigan February 17, 2026
    by Ted Corrigan February 17, 2026

    AI-driven analysis enabled by wearable devices has become an influential tool shaping modern clinical research. The technology embedded in today’s clinical trial wearables has evolved into a meaningful scientific and operational capability that can influence how studies are designed, conducted, and interpreted. While the use of…

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  • Ancillary Trial Supplies and EquipmentBusiness InsightsLife-Science Events

    From Operations to Strategy: What SCOPE 2026 Revealed About the Future of Clinical Supply and RTSM

    by Dan McDonald February 5, 2026
    by Dan McDonald February 5, 2026

    The center of gravity in clinical trials is shifting. Conversations that once lived in separate silos, such as vendor onboarding, randomization, and trial supply management (RTSM), are now deeply interconnected. That reality was on full display while chairing the IRT/RTSM: Navigating the Digital Neighborhood component of…

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Imperial Clinical Research Services Blog

Imperial is a global leader in clinical trial solutions and support, specializing in study and site print materials, ancillary trial supplies and equipment, clinical trial translation management, and clinical trial patient engagement.

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