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PET-MRI for Functional Imaging of the Testis: A Feasibility Study

NYU Langone Health logo

NYU Langone Health

Status

Withdrawn

Conditions

Vasectomy
Infertility
Non-obstructive Azoospermia

Treatments

Device: PET/ MRI of the Testis

Study type

Interventional

Funder types

Other

Identifiers

NCT02669108
14-01636

Details and patient eligibility

About

The primary objective of this study is to explore feasibility of testis functionality assessment and testis imaging obtained from Positron Emissions Tomography (PET) /Magnetic Resonance Imagine (MRI). Using advanced MRI metrics, investigators will study the three-dimensional structure of normal testis, the levels of specific elements and compounds in the tissues (which can only be found via these imaging techniques), and the directionality (and alterations in directionality) of tissue structure. Investigators hope to develop hypothesis that will in turn suggest bio-markers to be explored in subsequent clinical trials.

Sex

Male

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Men with proven paternity desiring vasectomy who are over 18 years of age.

Exclusion criteria

  • Bilaterally absent testes, unilaterally or bilaterally undescended testes
  • Patients who have proven azoospermia or no proven paternity
  • Inability to tolerate MRI including conditions such as claustrophobia or inability to lay flat for > 45 minutes.
  • Presence of pacemaker/IImplantable Cardioverter Defibrillator (ICD) or perfusion pumps
  • Ferromagnetic implants such as aneurysm clips, surgical clips, prostheses, artificial heart, valves with steel parts, metal fragments, shrapnel, bullets, tattoos near the eye, or steel implants.
  • Substance abuse, medical, psychological, or social conditions that may interfere with the patient's participation in the study
  • All women are excluded as such patients do not have the relevant anatomy being considered in this study
  • Anyone from a vulnerable population will be excluded from the study

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

PET/MRI of the Testis
Other group
Description:
PET/MRI of the testis will be performed upon the patient achieving azoospermia (following the vasectomy), or 25 ejaculations and following proven azoospermia (via standard of care semen analysis).
Treatment:
Device: PET/ MRI of the Testis

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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