ID

37739

Beskrivning

Study ID: 104864/517 Clinical Study ID: 104864/517 Study Title: A Phase I Study of Oral Topotecan as a Radiosensitizing Agent in Patients With Rectal Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00158886 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Topotecan + Radiation therapy Trade Name: N/A Study Indication: Rectal Cancer, Carcinoma, Renal Cell

Nyckelord

Versioner (1)
  1. 2019-08-21 2019-08-21 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

21 augusti 2019

DOI

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Licens

Creative Commons BY-NC 3.0
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Oral Topotecan as Radiosensitizing Agent in Patients with Rectal Cancer; NCT00158886

Engelsk

Laboratory Reference Ranges

1 Formulär  
Administrative Data
Beskrivning

Administrative Data

Alias
UMLS CUI-1
C1320722
Center number
Beskrivning

Study Coordinating Center, Identification number

Datatyp

integer

Alias
UMLS CUI [1,1]
C2825181
UMLS CUI [1,2]
C1300638
Laboratory Reference Ranges
Beskrivning

Laboratory Reference Ranges

Alias
UMLS CUI-1
C0883335
Investigator
Beskrivning

Reference lab test reference range, Investigator Name

Datatyp

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C2826892
Test
Beskrivning

Reference lab test reference range, Laboratory procedures

Datatyp

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C0022885
Unit
Beskrivning

Reference lab test reference range, Laboratory Procedures, Unit of Measure

Datatyp

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C0022885
UMLS CUI [1,3]
C1519795
Low Reference Value
Beskrivning

Reference lab test reference range, Lower limit of reference range

Datatyp

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C1272773
High Reference Value
Beskrivning

Reference lab test reference range, Higher limit of reference range

Datatyp

text

Alias
UMLS CUI [1,1]
C0883335
UMLS CUI [1,2]
C1272773
Tillbaka till toppen

Similar models

Laboratory Reference Ranges

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Study Coordinating Center, Identification number
Item
Center number
integer
C2825181 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Item Group
Laboratory Reference Ranges
C0883335 (UMLS CUI-1)
Reference lab test reference range, Investigator Name
Item
Investigator
text
C0883335 (UMLS CUI [1,1])
C2826892 (UMLS CUI [1,2])
Item
Test
text
C0883335 (UMLS CUI [1,1])
C0022885 (UMLS CUI [1,2])
Reference lab test reference range, Laboratory procedures
Code List
Test
CL Item
Sodium (1)
CL Item
Potassium (2)
CL Item
Chloride (3)
CL Item
Bicarbonate (4)
CL Item
Calcium (5)
CL Item
BUN (6)
CL Item
Creatinine (7)
CL Item
Alkaline Phosphatase (8)
CL Item
SGOT/AST (9)
CL Item
SGPT/ALT (10)
CL Item
Total Bilirubin (11)
CL Item
Total Protein (12)
CL Item
Albumin (13)
CL Item
Creatinine Clearance (14)
CL Item
CEA (15)
CL Item
Protein (Urinalysis) (16)
CL Item
Glucose (Urinalysis) (17)
CL Item
Blood (Urinalysis) (18)
CL Item
RBC/HPF (19)
CL Item
WBC/HPF (20)
CL Item
Casts/LPF (21)
CL Item
Crystals/LPF (22)
Reference lab test reference range, Laboratory Procedures, Unit of Measure
Item
Unit
text
C0883335 (UMLS CUI [1,1])
C0022885 (UMLS CUI [1,2])
C1519795 (UMLS CUI [1,3])
Reference lab test reference range, Lower limit of reference range
Item
Low Reference Value
text
C0883335 (UMLS CUI [1,1])
C1272773 (UMLS CUI [1,2])
Reference lab test reference range, Higher limit of reference range
Item
High Reference Value
text
C0883335 (UMLS CUI [1,1])
C1272773 (UMLS CUI [1,2])
Tillbaka till toppen 

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