[PDF] Top 20 Efficacy and safety of Shenyankangfu tablets for primary glomerulonephritis: study protocol for a randomized controlled trial

... Frequency tables, percentages, or constituent ratios will be used to describe the categorical data. Mean and standard deviation or median, first quartile, and third quartile will be used to describe continuous data. Cat- ... See full document

... We have performed sample size calculations for chronic dizziness according to other studies on the same disease using the same primary outcome measure because no such acupuncture research has been reported ... See full document

... patients. Efficacy analyses will be per- formed for both the intent-to-treat (ITT) population and the per-protocol (PP) ...all randomized subjects who have been administered at least one ...clinical ... See full document

... side effects [7]. Moreover, overuse of these medicines has been found to result in drug-resistant strains [8]. Up to 2003, M2-resistant variants had even spread to countries where these drugs are used infrequently [9]. ... See full document

... (FFDS) tablets ( Radix Salviae miltiorrhizae formula tablets) are a traditional Chinese medicine that has been reported to improve ...FFDS tablets in clinical practice derives from methodologically ... See full document

... multicenter, randomized, open, assessor-blinded, parallel-group clinical ...The primary outcome measure is change in pain on a numerical rating scale (NRS) from week 1 to week ...L). Safety will be ... See full document

... ongoing study is a single-blind, single-center, parallel group, randomized controlled ...and randomized into either the EA group or the sham EA ...The primary outcome is Hamilton Rating ... See full document

... have been achieved when the subject feels localized tin- gling pain; the vaccaria seeds will then be fixed to pre- vent them from coming loose. We use small adhesive tape with spherical vaccaria seeds to adhere to the ... See full document

... this study will be performed by an independent professional statistician using PEMS ...per- protocol analysis will be restricted to participants who strictly follow the protocol and complete the ... See full document

... Neurocognitive deficits are common in patients with severe TBI. Patients who fail to fully recover conscious- ness may enter a disorder of consciousness (DOC) such as coma, a vegetative state, or a minimally conscious ... See full document

... the safety and efficacy of camostat mesilate, 200 mg three times daily, based on subjective complaints and objective find- ings in subjects treated for up to 8 weeks for AP and CP ...the efficacy ... See full document

... a randomized controlled trial of very early treatment of PDA within the first 12 h of life in newborns <29 weeks of gestation demonstrated that newborns who received early indomethacin had a lower ... See full document

... the safety and tolerability profile of the study drug dexa- methasone has been well-characterized, allowing a clear understanding of the difference between drug-related and disease-related ...this ... See full document

... The sample size calculation is based on the parametric evaluation of a two group comparison using a t-test though a more complex statistical model will be used as primary test. Based on data from the literature ... See full document

... This study is designed as a superiority trial based on pre- vious cohort ...the study, we decided to recruit 60 patients for both treatment groups in order to have sufficient statistical power ... See full document

... small randomized study conducted by Harrison [5] showed hCG to be significantly more effective than bed ...double-blind, randomized, placebo-controlled study was conducted in 183 women ... See full document

... our trial, we will ensure that all enrolled patients have estab- lished moderate/severe ARDS after 24 hours of meeting the AECC/Berlin definition while on standard ventilator ...will study is different from ... See full document

... randomised controlled studies, nor the reviews, which also included observational studies, could confirm the ...of safety, both in the short-term and in the oncological ...that safety and ... See full document

... The study design is a randomized controlled ...be randomized into one of two groups: acupuncture group (AG) (n = 33) and electroacupuncture group (EG) (n = ...The primary clinical ... See full document

... this study was deter- mined by power analysis based on the results of a previ- ous study with the same probiotic blend ...clinical trial within the last 30 days; or if compliance and completion of ... See full document