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Table representation of search results timeline featuring number of search results per year.

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1997 1
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2005 2
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2009 1
2010 1
2012 2
2013 1
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2018 2
2019 2
2020 1
2021 1
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Showing results for blind frangou
Your search for Blend Frangu retrieved no results
An Investigation of Levetiracetam in Alzheimer's Disease (ILiAD): a double-blind, placebo-controlled, randomised crossover proof of concept study.
Sen A, Akinola M, Tai XY, Symmonds M, Davis Jones G, Mura S, Galloway J, Hallam A, Chan JYC, Koychev I, Butler C, Geddes J, Van Der Putt R, Thompson S, Manohar SG, Frangou E, Love S, McShane R, Husain M. Sen A, et al. Trials. 2021 Jul 31;22(1):508. doi: 10.1186/s13063-021-05404-4. Trials. 2021. PMID: 34332638 Free PMC article. Clinical Trial.
We plan to recruit thirty patients with mild to moderate Alzheimer's disease with no history of previous seizures or other significant co-morbidity. Participants will be allocated to a double-blind placebo-controlled crossover trial that tests levetiracetam against placebo …
We plan to recruit thirty patients with mild to moderate Alzheimer's disease with no history of previous seizures or other significant co-mo …
Evaluating the effects of the novel GLP-1 analogue liraglutide in Alzheimer's disease: study protocol for a randomised controlled trial (ELAD study).
Femminella GD, Frangou E, Love SB, Busza G, Holmes C, Ritchie C, Lawrence R, McFarlane B, Tadros G, Ridha BH, Bannister C, Walker Z, Archer H, Coulthard E, Underwood BR, Prasanna A, Koranteng P, Karim S, Junaid K, McGuinness B, Nilforooshan R, Macharouthu A, Donaldson A, Thacker S, Russell G, Malik N, Mate V, Knight L, Kshemendran S, Harrison J, Hölscher C, Brooks DJ, Passmore AP, Ballard C, Edison P. Femminella GD, et al. Trials. 2019 Apr 3;20(1):191. doi: 10.1186/s13063-019-3259-x. Trials. 2019. PMID: 30944040 Free PMC article. Clinical Trial.
METHODS/DESIGN: ELAD is a 12-month, multi-centre, randomised, double-blind, placebo-controlled, phase IIb trial of liraglutide in participants with mild Alzheimer's dementia. ...
METHODS/DESIGN: ELAD is a 12-month, multi-centre, randomised, double-blind, placebo-controlled, phase IIb trial of liraglutide in par …
A systematic review on the role of anticonvulsants in the treatment of acute bipolar depression.
Reinares M, Rosa AR, Franco C, Goikolea JM, Fountoulakis K, Siamouli M, Gonda X, Frangou S, Vieta E. Reinares M, et al. Int J Neuropsychopharmacol. 2013 Mar;16(2):485-96. doi: 10.1017/S1461145712000491. Epub 2012 May 10. Int J Neuropsychopharmacol. 2013. PMID: 22575611 Free article. Review.
All anticonvulsants were generally well tolerated. No double-blind RCTs were found for the use of other anticonvulsants such as oxcarbazepine, licarbazepine, zonisamide, retigabine, pregabalin, tiagabine, felbamate and vigabatrine in the acute treatment of bipolar depressi …
All anticonvulsants were generally well tolerated. No double-blind RCTs were found for the use of other anticonvulsants such as oxcar …
Mechanism of action for leflunomide in rheumatoid arthritis.
Fox RI, Herrmann ML, Frangou CG, Wahl GM, Morris RE, Strand V, Kirschbaum BJ. Fox RI, et al. Clin Immunol. 1999 Dec;93(3):198-208. doi: 10.1006/clim.1999.4777. Clin Immunol. 1999. PMID: 10600330 Review.
Leflunomide (Arava) has recently been approved by the Food and Drug Administration for the treatment of rheumatoid arthritis (RA). This approval was based on data from a double-blind, multicenter trials in the United States (leflunomide versus methotrexate versus placebo) …
Leflunomide (Arava) has recently been approved by the Food and Drug Administration for the treatment of rheumatoid arthritis (RA). This appr …
Efficacy of ethyl-eicosapentaenoic acid in bipolar depression: randomised double-blind placebo-controlled study.
Frangou S, Lewis M, McCrone P. Frangou S, et al. Br J Psychiatry. 2006 Jan;188:46-50. doi: 10.1192/bjp.188.1.46. Br J Psychiatry. 2006. PMID: 16388069 Clinical Trial.
AIMS: To examine the efficacy of EPA in treating depression in bipolar disorder. METHOD: In a12-week, double-blind study individuals with bipolar depression were randomly assigned to adjunctive treatment with placebo (n=26) or with 1 g/day (n=24) or 2 g/day (n=25) of ethyl …
AIMS: To examine the efficacy of EPA in treating depression in bipolar disorder. METHOD: In a12-week, double-blind study individuals …
Is the prophylactic antidepressant efficacy of lithium in bipolar I disorder dependent on study design and lithium level?
Severus WE, Grunze H, Kleindienst N, Frangou S, Moeller HJ. Severus WE, et al. J Clin Psychopharmacol. 2005 Oct;25(5):457-62. doi: 10.1097/01.jcp.0000177550.13714.7a. J Clin Psychopharmacol. 2005. PMID: 16160621 Review.
To provide evidence-based guidelines on this issue, large prospective, randomized, double-blind, placebo-controlled trials are needed comparing the efficacy of lithium at different plasma levels against manic and depressive relapse/recurrence. ...
To provide evidence-based guidelines on this issue, large prospective, randomized, double-blind, placebo-controlled trials are needed …
Mirroring everyday clinical practice in clinical trial design: a new concept to improve the external validity of randomized double-blind placebo-controlled trials in the pharmacological treatment of major depression.
Severus E, Seemüller F, Berger M, Dittmann S, Obermeier M, Pfennig A, Riedel M, Frangou S, Möller HJ, Bauer M. Severus E, et al. BMC Med. 2012 Jul 2;10:67. doi: 10.1186/1741-7015-10-67. BMC Med. 2012. PMID: 22747667 Free PMC article.
BACKGROUND: Randomized, double-blind, placebo-controlled trials constitute the gold standard in clinical research when testing the efficacy of new psychopharmacological interventions in the treatment of major depression. However, the blinded use of placebo has been …
BACKGROUND: Randomized, double-blind, placebo-controlled trials constitute the gold standard in clinical research when testing the ef …
Neural correlates of liraglutide effects in persons at risk for Alzheimer's disease.
Watson KT, Wroolie TE, Tong G, Foland-Ross LC, Frangou S, Singh M, McIntyre RS, Roat-Shumway S, Myoraku A, Reiss AL, Rasgon NL. Watson KT, et al. Behav Brain Res. 2019 Jan 1;356:271-278. doi: 10.1016/j.bbr.2018.08.006. Epub 2018 Aug 9. Behav Brain Res. 2019. PMID: 30099030 Clinical Trial.
Liraglutide, a glucagon-like peptide-1 (GLP) agonist, is an insulin-sensitizing agent with neuroprotective properties, as shown in animal studies. The purpose of this double-blinded, placebo-controlled study was to examine the neural effects of administration of liraglutid …
Liraglutide, a glucagon-like peptide-1 (GLP) agonist, is an insulin-sensitizing agent with neuroprotective properties, as shown in animal st …
Effect of moderate to high intensity aerobic exercise on blood pressure in young adults: The TEPHRA open, two-arm, parallel superiority randomized clinical trial.
Williamson W, Lewandowski AJ, Huckstep OJ, Lapidaire W, Ooms A, Tan C, Mohamed A, Alsharqi M, Bertagnolli M, Woodward W, Dockerill C, McCourt A, Kenworthy Y, Burchert H, Doherty A, Newton J, Hanssen H, Cruickshank JK, McManus R, Holmes J, Ji C, Love S, Frangou E, Everett C, Hillsdon M, Dawes H, Foster C, Leeson P. Williamson W, et al. EClinicalMedicine. 2022 May 13;48:101445. doi: 10.1016/j.eclinm.2022.101445. eCollection 2022 Jun. EClinicalMedicine. 2022. PMID: 35706495 Free PMC article.
The control group were sign-posted to educational materials on hypertension and recommended lifestyle behaviours. Investigators performing statistical analyses were blinded to group allocation. The primary outcome was 24 h awake ambulatory blood pressure (systolic and dias …
The control group were sign-posted to educational materials on hypertension and recommended lifestyle behaviours. Investigators performing s …
Acute citalopram administration may disrupt contextual information processing in healthy males.
Almeida S, Glahn DC, Argyropoulos SV, Frangou S. Almeida S, et al. Eur Psychiatry. 2010 Mar;25(2):87-91. doi: 10.1016/j.eurpsy.2009.05.010. Epub 2009 Aug 19. Eur Psychiatry. 2010. PMID: 19695841 Clinical Trial.
Therefore, the purpose of this study was to identify the effect size of acute (within 24 hours) and chronic (28 days) administration of the highly selective SSRI, Citalopram, compared to placebo on response inhibition (measured by the Degraded Symbol Continuous Performance Task [ …
Therefore, the purpose of this study was to identify the effect size of acute (within 24 hours) and chronic (28 days) administration of the …
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