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Clinical Trials/DRKS00022361
DRKS00022361
Recruiting
未知

Prospective randomized analysis of psychological distress in men before, during, and after MR-fusion prostate biopsy depending on preoperative guidance

niversitätsklinikum Bonn Klinik und Kinderklinik für Urologie0 sites180 target enrollmentOctober 28, 2020
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ConditionsC61F41.3Malignant neoplasm of prostateOther mixed anxiety disorders

Overview

Phase
未知
Intervention
Not specified
Conditions
C61
Sponsor
niversitätsklinikum Bonn Klinik und Kinderklinik für Urologie
Enrollment
180
Status
Recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 28, 2020
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
Male

Investigators

Sponsor
niversitätsklinikum Bonn Klinik und Kinderklinik für Urologie

Eligibility Criteria

Inclusion Criteria

  • •Subjects will only be included in the study if they meet all of the following criteria:
  • •General inclusion criteria:
  • •Subjects: male, aged 45\-85
  • •Clinical suspicion of prostate cancer and MR\-fusion biopsy recommended to subject.
  • •Subject is able to follow the study instructions and likely to comply with all necessary study visits (compliance).
  • •Subject has given written consent to participate in the study.
  • •Indication\-specific inclusion criteria: none

Exclusion Criteria

  • •Subjects will not be included in the study if any of the following criteria applies:
  • •General Exclusion Criteria:
  • •Subject without legal capacity who is unable to understand the nature, scope, significance and consequences of this clinical trial
  • •Subjects with a physical or psychiatric condition which at the investigator’s discretion may put the subject at risk, may confound the trial results, or may interfere with the subject’s participation in this clinical trial
  • •Known or persistent abuse of medication, drugs or alcohol
  • •Contraindications for magnetic resonance imaging

Outcomes

Primary Outcomes

Not specified

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