ClinicalTrials.gg
Enrolling by invitationNCT07439913Updated Apr 27, 2026

Predictive Factors for 10-year Biochemical Recurrence and Urinary Continence Following Robot-assisted Radical Prostatectomy for Prostate Cancer

An observational study in Prostate Cancer (Adenocarcinoma), sponsored by F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica. Enrolling by invitation at 1 site in Slovakia. Open to male participants. Per ClinicalTrials.gov, last updated 2026-04-27.

Sponsored by F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
120
Sex
Male
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Study summary

The aim of the present project is to evaluate long-term oncological and functional treatment outcomes, as well as patient satisfaction, ten years after radical prostatectomy in patients initially enrolled in CPRRP study. This research builds on a previous five-year follow-up evaluation (approved by the ethics committee) and focuses on the durability of therapeutic effects, quality of life, and long-term complications. Data will be collected via telephone interviews assessing key parameters (PSA levels, information on subsequent radiotherapy and androgen-deprivation therapy, the ICIQ-SF and IIEF-5 questionnaires, and patient-reported quality-of-life and satisfaction measures), followed by statistical analysis.

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Conditions studied

  • Prostate Cancer (Adenocarcinoma)
03

In context

Prostatic Neoplasms

7,046 studies on the registry are indexed under Prostatic Neoplasms; 1,580 are open to participants now.

This study's planned enrollment of 120 is below the median of 200 across 1,310 observational studies indexed under Prostatic Neoplasms.

Browse Prostatic Neoplasms studies →

Lead sponsor

F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica is the lead sponsor of 9 studies on the registry; 3 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
Sampling method
Non-probability sample

Study population

All participats of the initial CPRRS study

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Robot assisted radical prostatectomy performed in CPRRP study

Exclusion criteria

Exclusion Criteria:

-

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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
120 participants (estimated)
Target follow-up
12 Months
Patient registry
Yes

Interventions

  • ProcedureRadical prostatectomy

    Robot assisted radical prostatectomy

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What researchers measure

Primary outcomes

  1. Biochemical recurrence

    Prostate cancer biochemical recurrence rate

    Time frame: From treatment to 10 years.

Secondary outcomes

  1. Incontinence rate

    Postprostatectomy incontinence

    Time frame: From surgery until 10 years.

  2. Erectile dysfunction rate

    Postprostatectomy erectile dysfunction rate

    Time frame: From surgery until 10 years.

07

Study locations

1 site
  • F.D. Roosvelt university hospital
    Banská Bystrica, Slovakia
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Started Feb 2026 (actual). Primary completion is estimated for Feb 2027, 12 months after the start.

Of 541 non-industry observational studies under Prostatic Neoplasms, half reached primary completion within 67 months of starting (the median), counting those still running; a quarter within 29 and three quarters within 162. This study's planned 12 months is below that.

Counting every sponsor, half of 650 studies reached it within 60 months; a quarter within 29 and three quarters within 141.

How these figures are worked out, and which studies are left out of them.

Registered
Feb 23, 2026
First posted
Feb 27, 2026
StartActual
Feb 1, 2026
Primary completionEst.
Feb 18, 2027
CompletionEst.
Feb 18, 2027
Last update
Apr 27, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 27, 2026, 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
NCT07439913
Lead sponsor
F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica
Responsible party
Viktor Kováčik (Doctor, F.D. Roosevelt Teaching Hospital with Policlinic Banska Bystrica) — Principal investigator
First posted
Feb 27, 2026
Start date
Feb 1, 2026
Primary completion
Feb 18, 2027 (estimated)
Completion
Feb 18, 2027 (estimated)
Last update
Apr 27, 2026

Oversight

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

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