
Designing the Future: Trials in Motion
New to this year’s Congress, Designing the Future: Trials in Motion is a dynamic session where SIU 2025 invites investigators to share clinical trials that are actively shaping the future of urologic care. This session will highlight trials that are about to launch, currently enrolling, or in follow-up, but yet to report out — spotlighting innovative designs and compelling scientific rationales. These presentations will offer a global platform to engage with peers and spark collaboration. Submissions should focus on trial design, objectives, and eligibility criteria, emphasizing the potential impact these trials may have on tomorrow’s practice.
Important Dates*
Submission Deadline
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Wednesday, August 6, 2025
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Notifications Sent to Presenting Author
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Wednesday, August 27, 2025
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Deadline for the presenting author to respond to the invitation and register
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Wednesday, September 17, 2025
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Session Date
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Saturday, November 1, 2025
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*subject to change
Registration
- The presenting author of each accepted submission must attend the SIU 2025 Congress in person in Edinburgh.
- Presenters must confirm their participation and complete their registration for SIU 2025 by Wednesday, September 17, 2025.
- Failure to register by the deadline will result in removal from the programme. Presenting authors may be changed up until the deadline, but any replacement must also be registered to attend. After this date, unavailability to present onsite will lead to automatic withdrawal.
Submission Guidelines
Eligible Studies & Acceptable Trial Types:
- ✅ Trials in progress from phase 1, 2, and 3 are eligible.
- ✅ Industry-sponsored and investigator-initiated trials are both accepted.
- 🧪 Trials may be:
- About to launch
- Actively recruiting
- In follow-up
- 📄 Submissions should outline:
- The trial’s purpose, design, and eligibility criteria
- No preliminary data or results should be included.
Requirements:
- ✅ Trials must be registered and currently open to patient enrolment.
- ❌ No interim data or results may be included.
- ❌ Proprietary drug names and manufacturer names are not allowed.
- ❌ No references to pricing, fees, or reimbursement information are permitted.
Publication
- This session is intended solely for informational and educational purposes regarding active clinical trials. Please note that any submissions or abstracts presented will not be published in the SIUJ.
Submissions Field Requirements
- All fields are mandatory.
- Ensure the accuracy of all submitted information, as post-submission modifications will not be permitted.
Category
- Adrenals
- Basic Science - Benign Diseases
- Bladder Cancer - Basic Science
- Bladder Cancer - Clinical
- BPO/LUTS
- Female Urology
- History of Medicine
- Infections and Inflammatory Diseases
- Infertility
- Kidney and Ureter, Benign Diseases
- Kidney and Ureteral Cancer - Basic Science
- Kidney and Ureteral Cancer - Clinical
- Minimally Invasive Surgery/Robotics
- Pediatric Urology
- Penis/Testis/Urethra: Cancer - Basic Science
- Penis/Testis/Urethra: Cancer - Clinical
- Penis/Testis: Benign Disease
- Prostate Cancer - Basic Science
- Prostate Cancer - Detection
- Prostate Cancer - Clinical Localized
- Prostate Cancer - Clinical Advanced
- Reconstruction
- Renal Transplantation
- Sexual Dysfunction
- Stones
- Evaluation & Medical Management
- Surgical Treatment
- Training and Education
- Trauma
- Voiding Dysfunction
- Other
Submission Title
- Limited to 100 characters (approximately 15 words).
Background
- Limited to 1200 characters (approximately 200 words).
- Should include:
- Scientific rationale
- Overview of interventions
- Description of any related correlative studies
Methods
- Limited to 2600 characters (approximately 350 words).
- Should include:
- Trial design and statistical approach, highlighting innovative elements.
- Planned treatments or interventions.
- Key eligibility criteria, especially any novel aspects.
- Current enrolment status (without reporting outcomes or endpoints).
- Phase 2/3 trials: indicate the number of patients enrolled to date.
- Phase 3 trials: may include recent data monitoring committee review updates
Trial Phase - Phase 1, 2 or 3.
Trial Sponsor
Clinical Trial Identifier Number
Presenting Author – (NOTE: All communication will be with the presenting author.)
- First name
- Last name
- Institution/Affiliation
- Email Address
- Ensure this email address is valid as all communication will be sent to the presenting author by email.)
- Cell Phone #
Co-Authors
- Include First Name, Last Name, Email, and Affiliation
Who Can Present
- ✅ Only trial investigators may present on behalf of a study.
- 🚫 Industry representatives are not permitted to present.
Review Criteria
- Scientific Merit – Does the study explore a significant and novel clinical question?
- Study Design – Are methodology and endpoints clearly articulated and appropriate?
- Collaboration Potential – Is there evidence of multicentre or multidisciplinary collaboration?
- Relevance – Is the topic of interest to the SIU 2025 community?
Presentation Details
- Presenters will be allocated approximately 10 minutes to share their study and engage with the audience – 4-minute presentation, 6-minute discussion/Q&A.
- Presentations will be made in English.
Communication
- All communication will be sent by email to the presenting author. Ensure the email address is valid.

Questions?