Monitoring of Safety and Tolerance of PICOPREP in Clinical Practice
NCT ID: NCT01748591
Last Updated: 2015-12-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
3324 participants
OBSERVATIONAL
2012-05-31
2015-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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PICOPREP treatment
PICOPREP powder for oral solution according to standard clinical practice
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Ferring Pharmaceuticals
INDUSTRY
Responsible Party
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Principal Investigators
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Clinical Development Support
Role: STUDY_DIRECTOR
Ferring Pharmaceuticals
Locations
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Nemocnice Rudolfa a Stefanie
Benešov, , Czechia
Nemocnice Blansko
Blansko, , Czechia
Nemocnice Břeclav
Břeclav, , Czechia
Soukrmá ambulance
Česká Lípa, , Czechia
Děčínská nemocnice
Děčín, , Czechia
Nemocnice Havlíčkův Brod
Havlíčkův Brod, , Czechia
Fakultní nemocnice Hradec Králové
Hradec Králové, , Czechia
Nemocnice Jablonec
Jablonec nad Nisou, , Czechia
Nemocnice Jihlava
Jihlava, , Czechia
Privátní GE
Jihlava, , Czechia
FN Olomouc
Olomouc, , Czechia
FN Bulovka
Prague, , Czechia
Privátní GE Praha 4
Prague, , Czechia
Sanatorium Sv.Anny
Prague, , Czechia
Thomayerova nemocnice
Prague, , Czechia
Všeobecná fakutlní nemocnice
Prague, , Czechia
Nemocnice Příbram
Příbram, , Czechia
Lužická nemocnice
Rumburk, , Czechia
Nemocnice Tábor
Tábor, , Czechia
Nemocnice Teplice
Teplice, , Czechia
Ústecká poliklinika
Ústí nad Labem, , Czechia
Nemocnice Znojmo
Znojmo, , Czechia
Countries
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Other Identifiers
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000062
Identifier Type: -
Identifier Source: org_study_id