ProsBiT: Turkish Prostate Biopsy Study
NCT07919379, Active not recruiting, Istanbul Medeniyet University
Trial 8
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | ProsBiT: Turkish Prostate Biopsy Study | ClinicalTrials.gov |
| NCT number | NCT07919379 | ClinicalTrials.gov |
| Status | Active not recruiting | ClinicalTrials.gov |
| Enrollment | 8,310 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Istanbul Medeniyet University | ClinicalTrials.gov |
| Conditions | Prostate Cancer (Adenocarcinoma), Prostatic Neoplams, Prostate Specific Antigen | ClinicalTrials.gov |
| First posted | 2026-11-05 | ClinicalTrials.gov |
| Last updated | 2026-11-05 | ClinicalTrials.gov |
Registered outcomes 6
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Detection rate of clinically significant prostate cancer | At biopsy pathology report (within 4 weeks after biopsy) | Proportion of men with clinically significant prostate cancer (ISUP grade group ≥2) on biopsy pathology, compared between transperineal and transrectal biopsy. | ClinicalTrials.gov |
| Secondary | Detection rate of any and clinically insignificant prostate cancer | At biopsy pathology report (within 4 weeks after biopsy) | Proportion of men with any adenocarcinoma and with ISUP grade group 1 cancer on biopsy pathology. | ClinicalTrials.gov |
| Secondary | Procedural pain | During the biopsy procedure | Visual analog scale (VAS) pain score, 0 (no pain) to 10 (worst pain), recorded at digital rectal examination, probe insertion, local anesthetic injection, right-lobe sampling, left-lobe sampling, and the end of the procedure. | ClinicalTrials.gov |
| Secondary | Patient acceptability | Immediately after the biopsy procedure | Proportion of men who would choose the same biopsy method again. | ClinicalTrials.gov |
| Secondary | Infectious complications | [Within 30 days after biopsy - follow-up window] | Proportion of men with post-biopsy infection (including cystitis, urethritis, epididymitis/orchitis) and sepsis. | ClinicalTrials.gov |
| Secondary | Bleeding complications | [Within 30 days after biopsy - follow-up window] | Proportion of men with hematuria, urethrorrhagia, or perineal hematoma, overall and by antithrombotic use. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|---|---|
| 33089586 | BACKGROUND | PubMed |
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)