All Versions

Contents

Index

Standard

HL7 - Version 2.3

2.1

2.2

2.3

2.3.1

2.4

2.5

2.6

2.7

2.8

2.9

2.3

2.3 DE

Events

Segments

Msg. Types

Msg. Structs

Data Elements

Tables

Data Structs

Segment CSP: Clinical Study Phase (Informationen zur Phase einer klinischen Studie)

Seq	Description	German Interpretation	Length	C.LEN	Table	r/o/c	Rep#	Item	Data Structure	Section
1	Study Phase Identifier	ID der Studienphase	..60			C		01051	CE	7.7.2.1
2	Date/time Study Phase Began	Zeitpunkt des Anfangs der Studienphase	..26			R		01052	TS	7.7.2.2
3	Date/time Study Phase Ended	Zeitpunkt des Endes der Studienphase	..26			O		01053	TS	7.7.2.3
4	Study Phase Evaluability	Auswertbarkeit der Studienphase	..60			O		01054	CE	7.7.2.4

Used within the following Events:

C01 SRM - Register a patient on a clinical trial (7.6.1)

C02 SRM - Cancel a patient registration on clin.trial (for clerical mistakes only) (7.6.1)

C03 SRM - Correct/update registration information (7.6.1)

C04 SRM - Patient has gone off a clinical trial (7.6.1)

C05 SRM - Patient enters phase of clinical trial (7.6.1)

C06 SRM - Cancel patient entering a phase (clerical mistake) (7.6.1)

C07 SRM - Correct/update phase information (7.6.1)

C08 SRM - Patient has gone off phase of clinical trial (7.6.1)

C09 CSU - Automated time intervals for reporting, like monthly (7.6.2)

C10 CSU - Patient completes the clinical trial (7.6.2)

C11 CSU - Patient completes a phase of the clinical trial (7.6.2)

C12 CSU - Update/correction of patient order/result information (7.6.2)

P07 PEX - Unsolicited initial individual product experience report (7.10.1)

P08 PEX - Unsolicited update individual product experience report (7.10.1)

Links to Other/Further HL7 Information

generated: Nov 24, 2020 (FO)

Health Level Seven, Int. (HQ)

HL7 Germany
HL7 Europe

Frank Oemig's HL7 Site
(Infos about the database)

HL7-Experts Network