CClinicalTrials.gg
Status unknownNCT05427864Updated Jun 28, 2022

Comparison of Multiparametric Prostate MRI and Ga-68 PSMA PET Imaging in Prostate Cancer Staging

An interventional study of Multiparametric Prostate MRI in Prostate Cancer and Prostate Cancer Stage, sponsored by Gulhane Training and Research Hospital. Status unknown at 1 site in Turkey. Open to male participants. Per ClinicalTrials.gov, last updated 2022-06-28.

Sponsored by Gulhane Training and Research Hospital · Not applicable, Interventional, and Diagnostic

The sponsor has not verified this record recently (last verified Jun 2022), so the status shown — last known as Recruiting — may be out of date.

From the registry’s dates

  • Registered 2 years 5 months after the study started (first participant enrolled Jan 2020, registered Jun 2022).
Phase
Not applicable
Study type
Interventional
Enrollment
47
Allocation
Not applicable
Sex
Male
01

Study summary

In this study, it is aimed to compare the lesion location, lesion size, local and distant metastases detection rates of Ga68 PSMA PET and Multiparametric Prostate MR imaging tests used in staging in patients diagnosed with prostate cancer.

The pathologies of the patients who were decided to undergo radical prostatectomy as a treatment will also be compared with the staging tests.

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Conditions studied

  • Prostate Cancer
  • Prostate Cancer Stage

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03

In context

Prostatic Neoplasms

6,370 studies on the registry are indexed under Prostatic Neoplasms; 1,400 are open to participants now.

This study's planned enrollment of 47 is below the median of 58 across 4,822 interventional studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

Gulhane Training and Research Hospital is the lead sponsor of 44 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Male
Accepts healthy volunteers
No

Inclusion criteria

  • diagnosed with prostate cancer
  • Gleason score 7 or above / 6 with high risk
  • No other treatment

Exclusion criteria

Exclusion Criteria:

  • treated with radiotherapy
  • treated with ADT
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
47 participants (estimated)

Interventions

  • Diagnostic testMultiparametric Prostate MRI

    Comparison of Ga68 PSMA PET and Multiparametric Prostate MR imaging tests used in staging in patients diagnosed with prostate cancer

    Also known as: Ga-68 PSMA PET

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What researchers measure

Primary outcomes

  1. Lesion location

    Both MRI and PET results will be compared. Lesion location will be defined as "left", "right", "apical", "basal", "midline".

    Time frame: Between prostate biopsy and curative treatment decision , usually 2 month

  2. Lesion Size

    Both MRI and PET results will be compared, Lesion size will be stated in milimeters.

    Time frame: Between prostate biopsy and curative treatment decision , usually 2 month

  3. Lymph node involvement

    Both MRI and PET results will be compared. Involvement will be stated as "exist", "non-exist".

    Time frame: Between prostate biopsy and curative treatment decision , usually 2 month

  4. Extraprostatic involvement

    Both MRI and PET results will be compared. Involvement will be stated as "exist" , "non-exist".

    Time frame: Between prostate biopsy and curative treatment decision , usually 2 month

  5. Local and distant metastasis

    Both MRI and PET results will be compared. Metastasis will be stated as "exist" , "non-exist".

    Time frame: Between prostate biopsy and curative treatment decision , usually 2 month

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Study locations

1 of 1 sites recruiting
  • Gulhane Research and Training Hospital
    Ankara, Etlik 06010, Turkey
    • Can Sicimli, M.D. · Contact · cansicimli@gmail.com · +905077287879
    • Can Sicimli, M.D. · Principal investigator
    • Selahattin Bedir, Prof. · Sub investigator
    • Kemal Niyazi Arda, Prof. · Sub investigator
    • Hatice Tuba Sanal, Prof. · Sub investigator
    • Alev Çınar, M.D. · Sub investigator
    Recruiting
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References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 28, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05427864
Lead sponsor
Gulhane Training and Research Hospital
Responsible party
Can Sicimli (Principal Investigator, Gulhane Training and Research Hospital) — Principal investigator
First posted
Jun 22, 2022
Start date
Jan 1, 2020
Primary completion
Jan 5, 2023 (estimated)
Completion
Mar 5, 2023 (estimated)
Last update
Jun 28, 2022

Study contacts

Can Sicimli, M.D.
Contact
cansicimli@gmail.com
+905077287879

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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