age at least 18 Years
Item
Alter mindestens 18 Jahre
boolean
C0001779 (UMLS CUI 2011AA)
397669002 (SNOMED CT 2011_0131)
Unilateral or bilateral primary open angle glaucoma, capsular glaucoma, pigmentary glaucoma or ocular hypertension.
Item
Unilateral or bilateral primary open angle glaucoma, capsular glaucoma, pigmentary glaucoma or ocular hypertension.
boolean
C0205092 (UMLS CUI 2011AA)
66459002 (SNOMED CT 2011_0131)
C0238767 (UMLS CUI 2011AA)
51440002 (SNOMED CT 2011_0131)
C0339573 (UMLS CUI 2011AA)
77075001 (SNOMED CT 2011_0131)
10036719 (MedDRA 14.1)
H40.11 (ICD-10-CM Version 2010)
365.11 (ICD-9-CM Version 2011)
C0011900 (UMLS CUI 2011AA)
439401001 (SNOMED CT 2011_0131)
MTHU008876 (LOINC Version 232)
C0206368 (UMLS CUI 2011AA)
111514006 (SNOMED CT 2011_0131)
10037118 (MedDRA 14.1)
365.52 (ICD-9-CM Version 2011)
C1411998 (UMLS CUI 2011AA)
46168003 (SNOMED CT 2011_0131)
365.13 (ICD-9-CM Version 2011)
C0028840 (UMLS CUI 2011AA)
4210003 (SNOMED CT 2011_0131)
10030043 (MedDRA 14.1)
H40.0 (ICD-10-CM Version 2010)
365.04 (ICD-9-CM Version 2011)
Patients currently on IOP reducing therapy: IOP >= 25mmHg (two IOP determinations at pre-study separated by at least one hour) OR Patients without IOP reducing therapy: IOP >= 30mmHg (two IOP determinations at pre-study separated by at least one hour).
Item
Patients currently on IOP reducing therapy: IOP >= 25mmHg (two IOP determinations at pre-study separated by at least one hour) OR Patients without IOP reducing therapy: IOP >= 30mmHg (two IOP determinations at pre-study separated by at least one hour).
boolean
C0150312 (UMLS CUI 2011AA)
52101004 (SNOMED CT 2011_0131)
C0332197 (UMLS CUI 2011AA)
2667000 (SNOMED CT 2011_0131)
C0021888 (UMLS CUI 2011AA)
41633001 (SNOMED CT 2011_0131)
MTHU034775 (LOINC Version 232)
C0442797 (UMLS CUI 2011AA)
260371004 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
History of acute angle closure or closed/barely open anterior chamber angle.
Item
History of acute angle closure or closed/barely open anterior chamber angle.
boolean
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C0205178 (UMLS CUI 2011AA)
272118002 (SNOMED CT 2011_0131)
C0429528 (UMLS CUI 2011AA)
251726002 (SNOMED CT 2011_0131)
C0429524 (UMLS CUI 2011AA)
251722000 (SNOMED CT 2011_0131)
Current use of contact lenses.
Item
Current use of contact lenses.
boolean
C0521116 (UMLS CUI 2011AA)
15240007 (SNOMED CT 2011_0131)
C1524063 (UMLS CUI 2011AA)
260676000 (SNOMED CT 2011_0131)
C0009836 (UMLS CUI 2011AA)
57368009 (SNOMED CT 2011_0131)
MTHU013784 (LOINC Version 232)
Ocular surgery or argon laser trabeculoplasty (ALT) within three months prior to pre-study visit.
Item
Ocular surgery or argon laser trabeculoplasty (ALT) within three months prior to pre-study visit.
boolean
C1705869 (UMLS CUI 2011AA)
422191005 (SNOMED CT 2011_0131)
C1319234 (UMLS CUI 2011AA)
404636007 (SNOMED CT 2011_0131)
Ocular inflammation/infection occurring within three months prior to pre-study visit.
Item
Ocular inflammation/infection occurring within three months prior to pre-study visit.
boolean
C0239429 (UMLS CUI 2011AA)
10015943 (MedDRA 14.1)
C0015403 (UMLS CUI 2011AA)
128351009 (SNOMED CT 2011_0131)
10015929 (MedDRA 14.1)
E11391 (CTCAE 1105E)
Hypersensitivity to benzalkonium chloride or to any other component of the study drug solutions.
Item
Hypersensitivity to benzalkonium chloride or to any other component of the study drug solutions.
boolean
C0020517 (UMLS CUI 2011AA)
418634005 (SNOMED CT 2011_0131)
T78.40 (ICD-10-CM Version 2010)
C0005026 (UMLS CUI 2011AA)
64686009 (SNOMED CT 2011_0131)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C1705248 (UMLS CUI 2011AA)
C0304229 (UMLS CUI 2011AA)
902003 (SNOMED CT 2011_0131)
Other abnormal ocular condition or symptom preventing the patient from entering the study, according to the investigator's judgement.
Item
Other abnormal ocular condition or symptom preventing the patient from entering the study, according to the investigator's judgement.
boolean
C0205161 (UMLS CUI 2011AA)
263654008 (SNOMED CT 2011_0131)
C1299003 (UMLS CUI 2011AA)
C0348080 (UMLS CUI 2011AA)
260905004 (SNOMED CT 2011_0131)
COND (HL7 V3 2006_05)
CL411789 (UMLS CUI 2011AA)
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
Cardiac failure, sinus bradycardia, second and third degree of atrioventricular block. (The routines for prescribing topical B-blocking agents will be followed.
Item
Cardiac failure, sinus bradycardia, second and third degree of atrioventricular block. (The routines for prescribing topical B-blocking agents will be followed.
boolean
C0018801 (UMLS CUI 2011AA)
155374007 (SNOMED CT 2011_0131)
10019279 (MedDRA 14.1)
428 (ICD-9-CM Version 2011)
E10124 (CTCAE 1105E)
C0085610 (UMLS CUI 2011AA)
49710005 (SNOMED CT 2011_0131)
10040741 (MedDRA 14.1)
R00.1 (ICD-10-CM Version 2010)
E10208 (CTCAE 1105E)
C0264906 (UMLS CUI 2011AA)
195042002 (SNOMED CT 2011_0131)
10003677 (MedDRA 14.1)
I44.1 (ICD-10-CM Version 2010)
C0151517 (UMLS CUI 2011AA)
27885002 (SNOMED CT 2011_0131)
10003673 (MedDRA 14.1)
I44.2 (ICD-10-CM Version 2010)
426.0 (ICD-9-CM Version 2011)
E10093 (CTCAE 1105E)
Bronchial asthma, history of bronchial asthma or chronic obstructive pulmonary disease. (The routines for prescribing topical B-blocking agents will be followed).
Item
Bronchial asthma, history of bronchial asthma or chronic obstructive pulmonary disease. (The routines for prescribing topical B-blocking agents will be followed).
boolean
CL421546 (UMLS CUI 2011AA)
392521001 (SNOMED CT 2011_0131)
C0004096 (UMLS CUI 2011AA)
195967001 (SNOMED CT 2011_0131)
10003553 (MedDRA 14.1)
MTHU020815 (LOINC Version 232)
J45 (ICD-10-CM Version 2010)
493 (ICD-9-CM Version 2011)
C0024117 (UMLS CUI 2011AA)
13645005 (SNOMED CT 2011_0131)
10009033 (MedDRA 14.1)
J44.9 (ICD-10-CM Version 2010)
496 (ICD-9-CM Version 2011)
Pregnancy
Item
Schwangerschaft
boolean
C0549206 (UMLS CUI 2011AA)
289908002 (SNOMED CT 2011_0131)
10036556 (MedDRA 14.1)
MTHU035048 (LOINC Version 232)
Women of childbearing potential who has not used adequate contraceptive methods during the last three months.
Item
Women of childbearing potential who has not used adequate contraceptive methods during the last three months.
boolean
C0043210 (UMLS CUI 2011AA)
224526002 (SNOMED CT 2011_0131)
C1148523 (UMLS CUI 2011AA)
C0237399 (UMLS CUI 2011AA)
C0420844 (UMLS CUI 2011AA)
169450001 (SNOMED CT 2011_0131)
Inability to adhere to treatment/visit plan.
Item
Inability to adhere to treatment/visit plan.
boolean
C1299582 (UMLS CUI 2011AA)
371151008 (SNOMED CT 2011_0131)
C1321605 (UMLS CUI 2011AA)
405078008 (SNOMED CT 2011_0131)
C0039798 (UMLS CUI 2011AA)
C1512346 (UMLS CUI 2011AA)
ENC (HL7 V3 2006_05)
C1301732 (UMLS CUI 2011AA)
397943006 (SNOMED CT 2011_0131)
Have participated in any other clinical study within one month prior to pre-study visit.
Item
Have participated in any other clinical study within one month prior to pre-study visit.
boolean
C0679823 (UMLS CUI 2011AA)
PART (HL7 V3 2006_05)
C0205394 (UMLS CUI 2011AA)
74964007 (SNOMED CT 2011_0131)
C0008976 (UMLS CUI 2011AA)
110465008 (SNOMED CT 2011_0131)
C0332152 (UMLS CUI 2011AA)
288556008 (SNOMED CT 2011_0131)
C2348558 (UMLS CUI 2011AA)