Translation of "completed study program" to Swedish language:
Examples (External sources, not reviewed)
| Eighteen patients completed the study. | Arton patienter fullföljde studien. |
| 150 AVONEX treated patients completed one year on study and 85 completed two years on study. | 150 AVONEX behandlade patienter deltog under ett år i studien och åttiofem under två år. |
| Twenty five patients completed the first study and entered an extension study. | Tjugofem patienter fullföljde studien och ingick sedan i en utökad studie. |
| Eighteen patients completed the study to week 48. | Arton patienter fullföljde studien till vecka 48. |
| 259 subjects who completed the pivotal study entered a long term extension study. | 259 personer som fullföljde studien övergick i en långtidsuppföljningsstudie. |
| Sixty two patients completed the study to week 96. | Sextiotvå patienter fullföljde studien till vecka 96. |
| (to be completed after the first study group meeting) | (formuleras efter studiegruppens första möte) |
| Going to study to get into the nursing program? | Plugga för att komma in i sköterske programmet? |
| 8 ranibizumab treated patients completed 24 months of this study. | 8 injektioner eller simulerade injektioner en gång i månaden under 3 månader i följd, och därefter administrerades en dos var tredje månad. |
| (The Commission expects to have completed the study by June 2005). | (Kommissionen räknar med att studien skall vara klar i juni 2005.) |
| (To be completed after the first meeting of the Study Group. | (Kompletteras efter studiegruppens första sammanträde. |
| In a second study, fifteen patients with left ventricular hypertrophy completed a 6 month placebo controlled study and entered an extension study. | I en andra studie fullföljde femton patienter med vänsterkammarhypertrofi en placebokontrollerad studie under sex månader och ingick sedan i en utökad studie. |
| An additional study was completed with intravenous administration of midazolam and EMEND. | Ytterligare en studie med intravenös administrering av midazolam och Emend har avslutats. |
| In SHEPHERD study, 96 of the 97 enrolled patients completed the study (one patient died following a thrombotic event). | I SHEPHERD studien fullföljde 96 av 97 rekryterade patienter studien (en patient dog efter en tromboshändelse). |
| A fourth study was completed with intravenous administration of midazolam and oral aprepitant. | En fjärde studie med intravenös administrering av midazolam och oralt aprepitant har genomförts. |
| Sixty one patients completed the study (35 patients received the recommended 400 100 mg twice daily dose throughout the study). | Sextioen patienter fullföljde studien (35 patienter fick den rekommenderade dosen 400 100 två gånger dagligen genom hela studien). |
| Forty six patients were included in the first trial and 41 completed the study. | Fyrtiosex patienter ingick i den första prövningen och 41 fullföljde studien. |
| Completed | Färdigt |
| completed | färdiga |
| completed | färdig |
| Completed | Färdiga |
| Completed | Slutförd |
| Completed | Klar |
| Completed | FärdigtJob state |
| Completed | Klar |
| Completed | Färdig |
| Twenty eight patients with mild to moderate type 1 Gaucher disease were enrolled in this 12 month non comparative study, and 22 patients completed the study. | Tjugoåtta patienter med mild till måttlig Gauchers sjukdom typ 1 inkluderades i denna 12 månaders , icke jämförande studie varav 22 patienter fullföljde studien. |
| Adjuvant taxane therapy was allowed only if it was completed at least 12 months prior to study entry. | Adjuvant taxanbehandling var tillåtet endast om den hade avslutats minst 12 månader innan studieinklusion. |
| The Committee also noted that the last study performed in infants below one year was completed in 2001. | Kommittén noterade även att den senaste studien på barn under ett år avslutades 2001. |
| program | program |
| Program | Program |
| Program | Program |
| Program | Program |
| program | programTag Type |
| Multinational Etoricoxib and Diclofenac Arthritis Long term (MEDAL) Program The MEDAL Program was a prospectively designed Cardiovascular (CV) Safety Outcomes Program of pooled data from three randomized, double blind active comparator controlled trials, the MEDAL study, EDGE II and EDGE. | MEDAL (Multinational Etoricoxib and Diclofenac Arthritis Long term) programmet |
Related searches: Completed Study Program - Study Study Program - Program Has Been Completed - Study Was Completed - Study Is Almost Completed - A Successfully Completed Study - I Completed My Study - All Participants Completed The Study - I Have Completed My Study - Has Completed A Study -
