Study Trial design No. of patients Randomisation Outcomes assessed

Slides:



Advertisements
Similar presentations
FRISC II: Fragmin and fast Revascularization during InStability in Coronary artery disease - LONG-TERM HEPARIN - Purpose To assess efficacy of long-term.
Advertisements

Update on Anti-platelets Gabriel A. Vidal, MD Vascular Neurology Ochsner Medical Center October 14 th, 2009.
CAPRIE: Clopidogrel versus Aspirin in Patients at risk of Ischemic Events Purpose To assess the relative efficacy of the antiplatelet drugs clopidogrel.
Clostridium difficile Prevention and Treatment Katrina Beining & Christina Gardner Introduction Clostridium difficile (C. diff) is a gram-positive, spore-forming.
BEAUTI f UL: morBidity-mortality EvAlUaTion of the I f inhibitor ivabradine in patients with coronary disease and left ventricULar dysfunction Purpose.
I n t r o d u c t i o n Arthropathy is commonly observed in patients with IBD. In daily practice, peripheral arthritis, axial arthritis or a combination.
ISIS-4: Fourth International Study of Infarct Survival Purpose To assess the separate and combined effects on all-cause mortality of adding early captopril,
COPERNICUS: Carvedilol Prospective Randomized Cumulative Survival trial Purpose To assess the effect of carvedilol, a β 1 -, β 2 - and α 1 -receptor blocker,
Amoxicillin for Acute Rhinosinusitis A Randomized Controlled Trial Garbutt JM, Banister C, Spitznagel E, Piccirillo JF. JAMA 2012;307(7): Prof.
Table 1 | Fibre in diverticulosis and symptomatic diverticular disease
1 Stone RM et al. Proc ASH 2015;Abstract 6.
Clinical outcomes among patients with chronic low back pain treated with pregabaline monotherapy in fort portal regional referral hospital, “case series”
EVOLUZIONE DEL RAPPORTO COSTO/EFFICACIA DELLA
FM Journal Club February, 2011.
Study Trial design No. of patients Randomisation Outcomes assessed
Study Trial design No. of patients Randomisation Outcomes assessed
Research where it is most needed National Respiratory Strategy
Pharmacological and Behavioral
Alcohol, Other Drugs, and Health: Current Evidence
Introduction Methods Results Conclusions
HOPE: Heart Outcomes Prevention Evaluation study
Copyright © 2003 American Medical Association. All rights reserved.
Neal B, et al. Diabetes Care 2015;38:403–411
One-Year rTMS Treatment for Refractory Trigeminal Neuralgia
Table 1 | Fibre in diverticulosis and symptomatic diverticular disease
CANTOS: The Canakinumab Anti-Inflammatory Thrombosis Outcomes Study
FATS- Familial Atherosclerosis Treatment Study
(p < for group 1 or 2 vs. group 3)
Effect of Chlorhexidine Gluconate and Benzydamine Hydrochloride Mouth Spray on Clinical Signs and Quality of Life of Patients with Streptococcal Tonsillopharyngitis:
Alcohol, Other Drugs, and Health: Current Evidence May-June, 2018
SAVE Trial design: Patients with moderate to severe obstructive sleep apnea (OSA) and known CV disease were randomized in a 1:1 fashion to either CPAP.
Volume 120, Issue 3, Pages (February 2001)
EUCLID Trial design: Patients with peripheral arterial disease (PAD) were randomized to ticagrelor 90 mg twice daily (n = 6,930) vs. clopidogrel 75 mg.
Cooperative North Scandinavian Enalapril Survival Study (CONSENSUS I)
EVITA Trial design: Smokers admitted with an acute coronary syndrome were randomized to varenicline 1 mg twice daily (n = 151) vs. placebo (n = 151). Study.
Volume 147, Issue 4, Pages (October 2014)
Efficacy and Safety of a Once-Daily Morphine Formulation in Chronic, Moderate-to- Severe Osteoarthritis Pain  Jacques R. Caldwell, MD, Ronald J. Rapoport,
CANOA Trial design: Patients undergoing percutaneous closure of an ASD with the Amplatzer Septal Occluder were randomized to aspirin 80 mg plus clopidogrel.
SIGNIFY Trial design: Participants with stable coronary artery disease without clinical heart failure and resting heart rate >70 bpm were randomized to.
Modified Rankin score 0-2
ATMOSPHERE Trial design: Patients with symptomatic heart failure were randomized in a 1:1:1 fashion to either aliskiren 300 mg once daily, enalapril 5.
CIBIS II: Cardiac Insufficiency Bisoprolol Study II
Mean ADHD-RS-IV Scores at End Point
NMDA-Receptor Antagonists in Neuropathic Pain
Efficacy of transdermal nitroglycerin combined with etodolac for the treatment of chronic post-thoracotomy pain: An open-label prospective clinical trial 
Montelukast for postinfectious cough in adults: a double-blind randomised placebo- controlled trial  Dr Kay Wang, DPhil, Surinder S Birring, MD, Kathryn.
Advances in Rheumatology
One-Year rTMS Treatment for Refractory Trigeminal Neuralgia
Efficacy and safety of niacin/laropiprant
HARMONIZE Trial design: Patients with hyperkalemia (K ≥5.1 mEq/L) were randomized in a 1:1:1:1.7 fashion to receive sodium zirconium cyclosilicate (ZS)
Adalimumab Induces Deep Remission in Patients With Crohn's Disease
Occurrence of morning symptoms
POPE-2 Trial design: Patients with moderate to large pericardial effusion after cardiac surgery were randomized to colchicine 2 mg loading dose, then 1.
Study design (A) and subject disposition (B).
Original Article Testosterone for Low Libido in Postmenopausal Women Not Taking Estrogen Susan R. Davis, M.D., Ph.D., Michele Moreau, M.D., Robin Kroll,
Indications: Complicated DD after 6/52
SOLID-TIMI 52 Trial design: Participants within 30 days of an acute coronary syndrome (ACS) were randomized to darapladib 160 mg daily (n = 6,504) versus.
The Research Question Lateral epicondylosis (tennis elbow) is common, debilitating and often refractory to routine care. Prolotherapy, an injection-based.
Independent baseline predictors of non-remission at 24 months of follow-up in the SWEFOT trial population. Independent baseline predictors of non-remission.
Least squares mean (LSM) changes from baseline in (A) Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue) Total score and (B) Ankylosing.
Change in APOC3 level in response to treatment with APOC3 antisense oligonucleotide ISIS Phase 2, randomised, double-blind, placebo-controlled study.
Daily percentages of probiotic oligotype reads found in the dolphin rectum samples. Daily percentages of probiotic oligotype reads found in the dolphin.
Illustration of a trial design to help evaluate the clinical accuracy of a test of ischaemia. Illustration of a trial design to help evaluate the clinical.
The correlation between allergic rhinitis and sleep disturbance
Section C: Clinical trial update: Oral antiplatelet therapy
Medical Scientific Experts
Christensen P, et al. Gastroenterology 2006;131:738–747
Days without gluten challenge
Spasticity as measured by mean combined scores on the modified Ashworth scale, before and after treatment, on each day of each phase of the trial. Spasticity.
Study design. Study design. Patients who completed the 8-week induction study and achieved clinical response-100 (decrease in Crohn's disease activity.
Presentation transcript:

Table 4 | Controlled trials in using probiotics for symptomatic diverticular disease Study Trial design No. of patients Randomisation Outcomes assessed Length of follow-up Results Annibal et al. Prospective, randomised, open- label 50 Group A, high-fibre diet alone; Group B, twice daily 1 sachet of probiotic Lactobacillus paracasei sub. paracasei F19 for 14c days/month + high- fibre diet); Group C twice daily 2 sachets of probiotic Lactobacillus paracasei sub. Paracasei F19 for 4 days/month+ high-fibre diet Decrease in VAS score after treatment in SUDD 6 months Bloating decreased significantly in Groups B and C (groupB: 4.6 + 2.6 vs. 2.3 + 2.0, P < 0.05, group C: 3.9 + 2.9 vs. 1.8 + 2.1, P < 0.05). Dughera et al. 83 Polybacterial lysate suspension of Escherichia coli + Proteus Vulgaris for 2 weeks every month plus fibre 15 g/day vs. fibre 15 g/day alone Prevention of diverticulitis recurrence 3 months Polybacterial lysate plus fibre had significant superiority to fibre alone at 1 and 3 months in controlling symptoms and preventing diverticulitis recurrence (P < 0.05 and P < 0.01 respectively) Lahner et al. 30 Methylcellulose 2 tablets/day vs. placebo 2 tablets/day Symptom score decreased significantly in the methylcellulose group (from 19 + 6 to 13 + 4, P < 0.01) but not in the placebo group (from 21 + 7 to 17 + 9, P = n.s.) Tursi et al. Double-blind, randomised, placebo-controlled 210 Mesalazine 800 mg twice a day and Mesalazine 800 mg twice a day + Lactobacillus casei 750 mg a day vs. Lactobacillus casei 750 mg a day vs. Placebo 12 months Remission was maintained in 93.33% in combined treatment group, 85.45% in probiotic group and 54% of placebo group (P = 0.0001)Acute diverticulitis occurred in 0% in combined treatment group, 1.82% in probiotic group and 12% in the placebo group (P = 0.003) Balsalazide 2.25 g daily for 10 days every month plus probiotic mixture VSL#3 450 billions/day for 15 days every month (Group A) vs. VSL#3 alone 450 billions/day for 15 days every month (Group B) 6.66% of group A and 13.33% of group B pts had recurrence of the disease (P = n.s.) VAS, Visual Analogic Scale; DD, diverticular disease; SUDD, symptomatic uncomplicated diverticular disease.