Comparison of therapeutic efficacy and safety of radiofrequency ablation of hepatocellular carcinomas between internally cooled 15-G and 17-G single electrodes 1 2H J PARK MD 1M W LEE 1K D SONG MD 1D I CHA 1H RHIM 1T W KANG MD 1S LIM MD and 1H K LIM MD Evaluation of safety and efficacy of hydroxychloroquine plus favipiravir drug regimen in comparison with hydroxychloroquine plus kaletra in hospitalized patients with COVID-19 Public title Efficacy of hydroxychloroquine plus favipiravir drug regimen in comparison with hydroxychloroquine plus kaletra in hospitalized patients with COVID-19

IRCT

Evaluation of safety and efficacy of hydroxychloroquine plus favipiravir drug regimen in comparison with hydroxychloroquine plus kaletra on the need for intensive care unit treatment in patients with COVID-19 a randomized multicenter parallel groups open label study Public title

Combination therapy with Glucagon-like peptide-1 receptor agonist (GLP-1RA) and basal insulin represents a new therapeutic option for diabetes mellitus We hypothesized that GLP-1RA plus basal insulin is more efficacious safer and tolerable than GLP-1RA for patients with type 2 diabetes mellitus (T2DM) Randomized controlled trials (RCTs) comparing GLP-1RA plus basal insulin vs GLP-1RA

Efficacy and safety of a novel dual modulator of adenosine triphosphate‐citrate lyase and adenosine monophosphate‐activated protein kinase in patients with hypercholesterolemia: results of a multicenter randomized double‐blind placebo‐controlled parallel‐group trial J Am Coll Cardiol 2013 62:1154–1162 Medline Google Scholar

Combination therapy with Glucagon-like peptide-1 receptor agonist (GLP-1RA) and basal insulin represents a new therapeutic option for diabetes mellitus We hypothesized that GLP-1RA plus basal insulin is more efficacious safer and tolerable than GLP-1RA for patients with type 2 diabetes mellitus (T2DM) Randomized controlled trials (RCTs) comparing GLP-1RA plus basal insulin vs GLP-1RA

Combination therapy with Glucagon-like peptide-1 receptor agonist (GLP-1RA) and basal insulin represents a new therapeutic option for diabetes mellitus We hypothesized that GLP-1RA plus basal insulin is more efficacious safer and tolerable than GLP-1RA for patients with type 2 diabetes mellitus (T2DM) Randomized controlled trials (RCTs) comparing GLP-1RA plus basal insulin vs GLP-1RA

Comparison of efficacy and safety with obinutuzumab plus

May 30 2020Comparison of efficacy and safety with obinutuzumab plus chemotherapy versus rituximab plus chemotherapy in patients with previously untreated follicular lymphoma: Updated results from the phase III Gallium Study Abstract No : 8023 Abstract Type : Poster Discussion Session Indication : Follicular Lymphoma Intervention : Obinutuzumab

population") To assess efficacy in a more homogenous patient popu-lation the Phase 2 study NCT01059864 and the Phase 3 ORAL Start study were excluded as patients did not have a prior inadequate response to DMARDs To allow comparison between randomized dose groups including a placebo control efficacy analyses did not in-clude LTE data

for safety and/or efficacy 6 The term 'hypoglycemia' was also used as a measure of comparative safety 7 Only standard regular original or immediate release tablet/capsule formulations were reviewed for pharmacokinetic safety or efficacy modified or extended release or other formulations were excluded from the review 8

Objective To compare the efficacy and safety of calcipotriol ointment versus betamethasone ointment versus calcipotriol plus betamethasone ointment in patients of vitiligo Methods Patients with vitiligo (n=159) were randomized in three equal groups A B and C Group A (n=53) applied topical calcipotriol ointment group B (n=53) applied topical

Oct 21 2005Efficacy and Safety of Symbicort Turbuhaler 160/4 5 g/Inhalation Two Inhalations Twice Daily Plus As-needed Compared With Seretide™ Diskus™ 50/500 g/Inhalation One Inhalation Twice Daily Plus Terbutaline Turbuhaler 0 4 mg/Inhalation As-needed - a 6-month Randomised Double-blind Parallel-group Active Controlled Multinational

The restricted expression pattern of B-cell maturation antigen (BCMA) makes it an ideal tumor-associated antigen (TAA) for the treatment of myeloma BCMA has been targeted by both CD3 bispecific antibody and antibody–drug conjugate (ADC) modalities but a true comparison of modalities has yet to be performed Here we utilized a single BCMA antibody to develop and characterize both a CD3

Furthermore as the first systematic review to the best of our knowledge to compare the efficacy and safety of sitagliptin and sulfonylurea therapies in the treatment of patients with type 2 diabetes mellitus experiencing inadequate glycemic control with metformin monotherapy this

Comparison Chart: Flea Tick Products - With so many flea and tick products available it can be difficult to determine which one is best for your pet This guide will help you navigate the world of flea and tick products to find the perfect option to keep your pet parasite free

Comparison of Single Intra

Background: Viscosupplementation has been widely used for the treatment of knee osteoarthritis Because we found no well-controlled trial comparing single-injection regimens of hyaluronan for knee osteoarthritis we compared the efficacy and safety of a single intra-articular injection of a novel cross-linked hyaluronan (HYA-JOINT Plus) with a single injection of Synvisc-One in patients with

Aug 29 2020Background Many sedative regimens have been studied with controversial efficiencies This study tried to assess the desirable and adverse effects of sodium thiopental–fentanyl (TF) with ketamine–propofol (KP) for procedural sedation and analgesia in the emergency department Methods After signing written consent patients were enrolled in this randomised double-blind trial to receive

REVOLUTION PLUS is a simple-to-apply quick-drying small-volume monthly topical solution that protects against fleas (Ctenocephalides felis) ticks (black-legged or deer tick (Ixodes scapularis) Gulf Coast tick (Amblyomma maculatum) and American dog tick (Dermacentor variabilis)) ear mites (Otodectes cynotis) roundworms (Toxocara cati) hookworms (Ancylostoma tubaeforme) and

Comparison of efficacy and safety of capecitabine and oxaliplatin (CAPOX) with epirubicin oxaliplatin plus capecitabine (EOX) as first line treatment for advanced gastric cancer (AGC) a randomized clinical study Smita Kayal x Smita Kayal Search for articles by this author

Comparison of the immunogenicity efficacy and safety of 10 ug and 20 ug of a hepatitis B vaccine: a prospective randomized trial BY E K YEOH * C L LAI t W K CHANGt AND H Y LO* * Queen Elizabeth Hospital Hong Kong t University Department of Medicine Queen Mary Hospital Hong Kong I Virus Unit Medical and Health Department Hong Kong

Therefore to say that there is equivalent efficacy and safety may be an oversimplification For the albuterol only treatment the doses compared were the standard label dose of 0 083% (2 5 mg in 3 mL of normal saline) with the standard continuous SVN and the 0 5% solution (2 5 mg in 0 5 mL) with the addition of 0 5 mL normal saline for a 1 mL

Objective To compare the efficacy and safety of calcipotriol ointment versus betamethasone ointment versus calcipotriol plus betamethasone ointment in patients of vitiligo Methods Patients with vitiligo (n=159) were randomized in three equal groups A B and C Group A (n=53) applied topical calcipotriol ointment group B (n=53) applied topical betamethasone dipropionate ointment and group C

A Phase 3 Open-Label Randomized Study to Compare the Efficacy and Safety of Rituximab Plus Lenalidomide (CC-5013) Versus Rituximab Plus Chemotherapy Followed by Rituximab in Subjects with Previously Untreated Follicular Lymphoma MD Anderson Study Status Not Accepting Treatment Agent

Comparison of the immunogenicity efficacy and safety of 10 ug and 20 ug of a hepatitis B vaccine: a prospective randomized trial BY E K YEOH * C L LAI t W K CHANGt AND H Y LO* * Queen Elizabeth Hospital Hong Kong t University Department of Medicine Queen Mary Hospital Hong Kong I Virus Unit Medical and Health Department Hong Kong

Aug 29 2020Background Many sedative regimens have been studied with controversial efficiencies This study tried to assess the desirable and adverse effects of sodium thiopental–fentanyl (TF) with ketamine–propofol (KP) for procedural sedation and analgesia in the emergency department Methods After signing written consent patients were enrolled in this randomised double-blind trial to receive

population") To assess efficacy in a more homogenous patient popu-lation the Phase 2 study NCT01059864 and the Phase 3 ORAL Start study were excluded as patients did not have a prior inadequate response to DMARDs To allow comparison between randomized dose groups including a placebo control efficacy analyses did not in-clude LTE data