attached an example
Herbert,
thanks. Your example was not complete (it was not a longtable). But after changing this within the table in Lyx, it is running. I attached the file again for convenience/comparing.
But when I copy your ERT to my longtable, I get the following error message from Lyx:
"Extra alignment tab has been changed to \cr. &
You have given more \span or & marks than there were in the preamble to the \halign or \valign now in progress. So I'll assume that you meant to type \cr instead."
Do you have an idea, why my table is not processed?
Thanks
Michael
#LyX 1.3 created this file. For more info see http://www.lyx.org/ \lyxformat 221 \textclass article \language ngerman \inputencoding auto \fontscheme default \graphics default \paperfontsize default \papersize Default \paperpackage a4 \use_geometry 0 \use_amsmath 0 \use_natbib 0 \use_numerical_citations 0 \paperorientation portrait \secnumdepth 3 \tocdepth 3 \paragraph_separation indent \defskip medskip \quotes_language english \quotes_times 2 \papercolumns 1 \papersides 1 \paperpagestyle default
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CONSORT-Statement
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\begin_inset Tabular
<lyxtabular version="3" rows="29" columns="4">
<features islongtable="true">
<column alignment="left" valignment="top" leftline="true" width="40mm">
<column alignment="left" valignment="top" leftline="true" width="13mm">
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\begin_inset ERT
status Collapsed
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\backslash
caption{a caption for a longtable}%
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Publikationsabschnitt
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Beschreibung
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Erw�hnt auf Seite:
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1 Titel und Zusammenfassung
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1
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Zuordnung zu Therapiegruppen (z.B.
"randomisierte Verteilung", "randomisiert", oder "randomisierte Zuweisung").
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2 Einleitung
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<row>
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2.1 Hintergrund
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2
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Wissenschaftlicher Hintergrund und Begr�ndung der Studie.
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3 Methoden
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\end_inset
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\end_inset
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\layout Standard
\end_inset
</cell>
</row>
<row>
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3.1 Probanden/ Patienten
\end_inset
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3
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Einschlu�kriterien der Probanden/Patienten, Studienorganisation und Ort
der Studiendurchf�hrung (z.B.
im Krankenhaus oder nicht-station�r).
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\layout Standard
\end_inset
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<row>
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3.2 Intervention/ Behandlung
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4
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Pr�zise Angaben zu den geplanten Interventionen jeder Gruppe und zur Durchf�hrun
g.
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\begin_inset Text
\layout Standard
\end_inset
</cell>
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<row>
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3.3 Ziele
\end_inset
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5
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Genaue Ziele, Fragestellung und Hypothesen.
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3.4 Ergebnisse
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6
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Klar definierte prim�re und sekund�re Zielkriterien und, gegebenenfalls,
alle zur Optimierung der Ergebnisqualit�t verwendeten Methoden (z.B.
Mehrfachbeobachtungen, Training der Pr�fer)
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3.5 Fallzahlbestimmung
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7
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Wie wurden die Fallzahlen bestimmt und, falls notwendig, Beschreibung von
Zwischenanalysen und Kriterien f�r einen vorzeitigen Studienabbruch.
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3.6 Randomisierung
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\end_inset
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3.6.1 Erzeugung der Behandlungsfolge
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8
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Methode zur Generierung der zuf�lligen Zuteilung, einschlie�lich aller Einzelhei
ten (wie z.B.
Block-Randomisierung, Stratifizierung).
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3.6.2 Geheimhaltung der Behandlungsfolge (allocation concealment)
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9
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Durchf�hrung der Zuteilung (z.B.
numerierte Beh�lter; zentrale Randomisierung per Fax/Telefon).
Angabe, ob Geheimhaltung bis zur Zuteilung gew�hrleistet war.
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3.6.3 Durchf�hrung
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10
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Wer f�hrte die Zuteilung durch, wer nahm die Probanden/Patienten in die
Studie auf und wer teilte die Probanden/Patienten den Gruppen zu.
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3.6.4 Verblindung
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11
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Waren
\layout Standard
a) die Probanden/Patienten und/oder
\layout Standard
b) diejenigen, die die Intervention/Behandlung durchf�hrten und/oder
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c) diejenigen, die die Zielgr��en beurteilten verblindet oder nicht verblindet.
Wie wurde der Erfolg der Verblindung evaluiert?
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\end_inset
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3.7 Statistische Methoden
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12
\end_inset
</cell>
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Statistische Methoden zur Bewertung des prim�ren Zielkrieriums; weitere
Analysen, wie z.B.
Subgruppenanalysen und adjustierte Analysen.
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\emph on
4 Ergebnisse
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\end_inset
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\end_inset
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\end_inset
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4.1 Ein- und Ausschl�sse
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13
\end_inset
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Anzahl der Studienteilnehmer f�r jede Behandlungsgruppe, die
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a) gem�� Randomisierung gebildet wurde,
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b) tats�chlich die geplante Behandlung/Intervention erhalten haben,
\layout Standard
c) die Studie protokollgem�� beendeten,
\layout Standard
d) in der Analyse des prim�ren Zielkriteriums ber�cksichtigt wurden (Darstellung
in Flu�diagramm empfohlen).
Beschreibung von Protokollabweichungen mit Angabe von Gr�nden.
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4.2 Aufnahme/ Rekrutierung
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14
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N�here Angaben �ber den Zeitraum der Studienaufnahme der Probanden/Patienten
und der Nachbeobachtung.
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\end_inset
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<row>
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4.3 Patientencharakteristika zu Studienbeginn (baseline data)
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15
\end_inset
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Demografische und klinische Charakteristika aller Gruppen.
\end_inset
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\end_inset
</cell>
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<row>
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4.4 Anzahl der ausgewerteten Probanden/ Patienten
\end_inset
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\begin_inset Text
\layout Standard
16
\end_inset
</cell>
<cell alignment="center" valignment="top" topline="true" leftline="true" usebox="none">
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Anzahl der Probanden/Patienten (Nenner) in jeder Gruppe, die in die entsprechend
e Analyse eingeschlossen wurden und Angabe, ob es sich dabei um eine "Intention-
to-Treat" Analyse handelt.
Wenn m�glich, Angabe der Ergebnisse in absoluten Zahlen (z.B.
10 von 20, nicht 50%).
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\end_inset
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<row>
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4.5 Ergebnisse und Sch�tzmethoden
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\layout Standard
17
\end_inset
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Zusammenfassung der Ergebnisse aller prim�ren und sekund�ren Zielkriterien
f�r jede Gruppe und die gesch�tzte Effektgr��e sowie ihre Pr�zision (z.B.
95%-Konfidenzintervall).
\end_inset
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\end_inset
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4.6 Zus�tzliche Analysen
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18
\end_inset
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Angabe von weiteren Tests, insbesondere von Subgruppenanalysen und adjustierte
Analysen (mit Erkl�rung, ob sie vorher geplant waren oder nachtr�glich
durchgef�hrt wurden).
\end_inset
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\end_inset
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4.7 Unerw�nschte Wirkungen
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19
\end_inset
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Angabe aller wichtigen unerw�nschten Wirkungen oder Nebenwirkungen innerhalb
jeder Behandlungsgruppe.
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\emph on
5 Diskussion
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\end_inset
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5.1 Interpretation
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Interpretation der Ergebnisse unter Ber�cksichtigung der Studienhypothesen,
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Testen und multiple Zielkriterien.
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5.2 Generalisierbarkeit
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Generalisierbarkeit der Studienergebnisse (externe Validit�t).
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5.3 Bewertung der Evidenz
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Allgemeine Interpretation der Ergebnisse unter Ber�cksichtigung des aktuellen
Forschungsstandes und anderer Publikationen zur untersuchten Fragestellung.
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