ID

34478

Descripción

A Phase 1 Pilot Study of 99mTc-MIP-1404 SPECT/CT Imaging to Histology in Men With Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01615406

Link

https://clinicaltrials.gov/show/NCT01615406

Palabras clave

  1. 17/1/19 17/1/19 -
  2. 22/5/19 22/5/19 -
  3. 23/5/19 23/5/19 - Sarah Riepenhausen
Titular de derechos de autor

see on clinicaltrials.gov

Subido en

17 de enero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0

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Eligibility Prostate Cancer NCT01615406

Eligibility Prostate Cancer NCT01615406

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
male aged 21 years or older.
Descripción

ID.1

Tipo de datos

boolean

ability to provide signed informed consent and willingness to comply with protocol requirements.
Descripción

ID.2

Tipo de datos

boolean

past biopsy indicating the presence of adenocarcinoma of the prostate gland.
Descripción

ID.3

Tipo de datos

boolean

participant is deemed to have tissue suspicious of prostate cancer involvement that is amenable to biopsy/resection.
Descripción

ID.4

Tipo de datos

boolean

have had, or will undergo diagnostic ct or mri imaging prior to surgery.
Descripción

ID.5

Tipo de datos

boolean

participants must agree to use an acceptable form of birth control throughout the study period. participants must use condoms for a period of seven days after study drug administration, if engaged in sexual activity.
Descripción

ID.6

Tipo de datos

boolean

Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
participants for whom participating would significantly delay the scheduled standard of care therapy.
Descripción

ID.7

Tipo de datos

boolean

participants administered a radioisotope within 5 physical half lives prior to study enrollment.
Descripción

ID.8

Tipo de datos

boolean

participants with any medical condition or other circumstances that, in the opinion of the investigator, would significantly decrease obtaining reliable data, achieving study objectives or completing the study.
Descripción

ID.9

Tipo de datos

boolean

Similar models

Eligibility Prostate Cancer NCT01615406

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
male aged 21 years or older.
boolean
ID.2
Item
ability to provide signed informed consent and willingness to comply with protocol requirements.
boolean
ID.3
Item
past biopsy indicating the presence of adenocarcinoma of the prostate gland.
boolean
ID.4
Item
participant is deemed to have tissue suspicious of prostate cancer involvement that is amenable to biopsy/resection.
boolean
ID.5
Item
have had, or will undergo diagnostic ct or mri imaging prior to surgery.
boolean
ID.6
Item
participants must agree to use an acceptable form of birth control throughout the study period. participants must use condoms for a period of seven days after study drug administration, if engaged in sexual activity.
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
participants for whom participating would significantly delay the scheduled standard of care therapy.
boolean
ID.8
Item
participants administered a radioisotope within 5 physical half lives prior to study enrollment.
boolean
ID.9
Item
participants with any medical condition or other circumstances that, in the opinion of the investigator, would significantly decrease obtaining reliable data, achieving study objectives or completing the study.
boolean

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