ID
34419
Beschreibung
Study ID: 101998 Clinical Study ID: 101998 Study Title: A randomized, double-blind, parallel group, placebo-controlled, single-attack evaluation of the efficacy and tolerability of TREXIMA™ (sumatriptan 85mg/naproxen sodium 500mg)* tablets vs placebo when administered during the mild pain phase of a migraine Patient Level Data Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier Sponsor GlaxoSmithKline Collaborators N/A Phase Phase 3 Study Recruitment Status Completed Generic Name sumatriptan Trade Name Imitrex ,Imiject ,Imigran Study Indication Migraine Disorders This document asks if the subject is of child-bearing potential and which birth control methods the subject is using to prevent pregnancy during the study. This form should be filled out for female subjects at the screening visit.
Stichworte
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Rechteinhaber
GlaxoSmithKline
Hochgeladen am
17. Januar 2019
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Efficacy and Tolerability of TREXIMA Tablets vs. Placebo During Mild Migraine Study ID 101998
Child Bearing Potential and Birth Control
- StudyEvent: ODM
Beschreibung
Child-Bearing Potential
Alias
- UMLS CUI-1
- C3831118
Beschreibung
Complete for female subjects only - Pre-menarcheal: Females who have not begun to menstruate. - Post-menopausal: Women who have completed menopause at least one year ago. - Sterile: Pre-menopausal women who cannot conceive children. (This category includes women who have become sterile through surgical procedures such as tubal ligation. Do not include post-menopausal women in this category.) - Potentially able to bear children: Women of child-bearing age who are not sterile. Note: If the subject is sterile and is not of child-bearing age, then ‘post-menopausal’ will be the best choice and should be ticked. If the subject is sterile and does not know if she is post-menopausal and is less than 62 years of age, then she is of child-bearing age and ‘sterile’ should be ticked.
Datentyp
integer
Alias
- UMLS CUI [1]
- C3831118
Beschreibung
Birth Control Methods
Alias
- UMLS CUI-1
- C0700589
Beschreibung
Oral contraceptive
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0009905
Beschreibung
Intrauterine contraceptive device
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0021900
Beschreibung
Depot contraceptive (implants, injectables)
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0700589
- UMLS CUI [1,2]
- C0086129
Beschreibung
Spermicide plus physical barrier
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0037862
- UMLS CUI [1,2]
- C0004764
Beschreibung
Barrier method only if used in combination with any of the other acceptable contraception methods.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0004764
- UMLS CUI [2]
- C0042241
- UMLS CUI [3]
- C3873750
Beschreibung
Abstinence
Datentyp
boolean
Alias
- UMLS CUI [1]
- C3843422
Beschreibung
Sterilization of male partner
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0024559
Beschreibung
Other
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0205394
Beschreibung
Other Specification
Datentyp
text
Alias
- UMLS CUI [1,1]
- C0205394
- UMLS CUI [1,2]
- C2348235
Ähnliche Modelle
Child Bearing Potential and Birth Control
- StudyEvent: ODM
C0086129 (UMLS CUI [1,2])
C0004764 (UMLS CUI [1,2])
C0042241 (UMLS CUI [2])
C3873750 (UMLS CUI [3])
C2348235 (UMLS CUI [1,2])
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