Clinical trial · Interventional
CamPROBE: Developing a Safer and Simple Device for Local Anaesthetic Transperineal Prostate Biopsies
NCT03609528CI-TRIAL-00042120CamPROBEcompletedN/AClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The CamPROBE study investigates the rate of infective complications using the Cambridge Prostate Biopsy Device method of local anaesthetic transperineal prostate biopsies.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Prostate Cancer | Malignant Prostate Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| CamPROBE | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- CamPROBE biopsy method
- description
- To be completed
- interventionNames
- Device: CamPROBE
Primary outcomes (1)
- measure
- Incidence of Infection
- timeFrame
- 30 days post biopsy
- description
- Changes in incidence of infection as measured using patient self-reported Follow-Up Questionnaires and telephone assessments.
Secondary outcomes (3)
- measure
- Patient reported pain score
- timeFrame
- 30 days post biopsy
- description
Eligibility
Eligibility (as posted)
- Sex
- Male
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: To be included in the clinical investigation the participant must: * Have given written informed consent to participate * Be aged 18 years and over * Be suitable for a prostate biopsy and clinically due to have a biopsy for diagnostic or surveillance purposes * Be willing and able to comply with scheduled visits and completion of study questionnaires Exclusion Criteria: The presence of any of the following will preclude participant inclusion: * Contraindication to a prostate biopsy * Previous perineal or anal surgery * Unable to lie down with legs in a stirrup for at least 45 minutes, as assessed by a clinician
References
Publications (0)
Data not yet available
No reference posted for this study.