Clinical trial Recruiting at 1 site Observational Ages 15 to 90 Men only

MRI-DTI look at the urethral sphincter ring and prostate base shape

Official title: An Observational Study of the Relationship Between the Urethral Internal Sphincter Ring and Prostate Base Morphology Using MRI-DTI Fiber Tracking

Run by Jiangsu Taizhou People's Hospital · NCT07694752 · Data updated 2026-11-12

This imaging study tests how the male urethral internal sphincter ring appears on MRI-DTI and how it relates to prostate base morphology in men undergoing clinically indicated MRI.

Quick facts

Study typeObservational
Ages15 Years to 90 Years
SexMen only
Enrollment80 (estimated)
SponsorJiangsu Taizhou People's Hospital
Academic / other
Locations1 site (Taizhou, Jiangsu)
StatusRecruiting
StartedJuly 15, 2026
Main results expectedAugust 1, 2027
Study endsJune 1, 2028
Registry record updatedJuly 20, 2026
Trial IDNCT07694752 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Male patients undergoing clinically indicated pelvic, seminal vesicle, or prostate MRI-DTI, including those with suspected benign prostatic enlargement, cryptorchidism-associated imaging, suspected seminal vesiculitis, or planned ADT for prostate cancer.

Probably not a fit

Patients with markedly atypical anatomy or poor-quality MRI-DTI data may not gain direct benefit from the study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a single-center, observational imaging study using diffusion tensor imaging to visualize the ring-like structure of the male urethral internal sphincter and to explore its relationship with prostate base morphology. Participants include men undergoing pelvic, seminal vesicle, or prostate-related MRI-DTI for clinical reasons, with subgroups for those with benign prostatic enlargement or prostate cancer planned for androgen deprivation therapy. The study combines DTI with T2-weighted imaging, using fiber tracking and 3D reconstruction to characterize spatial relationships in the bladder neck, prostate base, and proximal urethra. It aims to provide in vivo descriptions of sphincter morphology under varying prostate conditions and during ADT follow-up where applicable.

Why it matters

Potential benefit: If successful, the findings could improve understanding of urethral sphincter anatomy in relation to the prostate and potentially inform surgical or treatment planning.

How similar studies have gone: Previous work in MRI-DTI has shown feasibility in visualizing pelvic floor structures, supporting the potential value of this approach in mapping the urethral sphincter.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Male participants undergoing clinically indicated pelvic, seminal vesicle, or prostate-related MRI-DTI examination.
2. Participants with adequate T2-weighted MRI and DTI data for post-processing and quantitative assessment of the bladder neck, prostate base, and proximal urethral region.
3. Participants in the cross-sectional imaging cohort may include men undergoing MRI for suspected cryptorchidism, suspected seminal vesiculitis, benign prostatic enlargement, or other clinically indicated pelvic or prostate-related evaluations.
4. Participants in the ADT paired follow-up cohort must have prostate cancer and be scheduled to receive androgen deprivation therapy, with MRI-DTI planned before treatment and during follow-up after ADT.
5. Participants must be able to comply with MRI examination procedures.
6. Written informed consent will be obtained when required by the approved study protocol.

Exclusion Criteria:

1. Contraindications to MRI, including but not limited to incompatible metallic implants, severe claustrophobia, or other conditions preventing MRI examination.
2. Known neurogenic bladder dysfunction, including spinal cord injury, multiple sclerosis, Parkinson disease, or other neurological disorders that may significantly affect lower urinary tract function.
3. History of pelvic radiotherapy.
4. History of urethral reconstruction, sphincter surgery, or other prior surgery that substantially alters the bladder neck, proximal urethra, or prostate base anatomy.
5. Severe cardiopulmonary dysfunction, cognitive impairment, psychiatric disorder, or other conditions preventing cooperation with MRI examination or study procedures.
6. Use of medications or treatments within the previous 3 months that may substantially affect neuromuscular function of the lower urinary tract, as judged by the investigators.
7. Poor image quality or failed post-processing that prevents reliable visualization or measurement of the urethral internal sphincter ring.

Where it's running

  • JiangsuTaizhouPH
    Taizhou, Jiangsu, China
    Recruiting

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.