Introduction to Randomised Double Blind

What is/are Randomised Double Blind?

Randomised Double Blind - SUMMARY: This randomised double blind study was designed to evaluate the analgesic efficacy of bupivacaine with verapamil mixture given through lumbar epidural route for postoperative analgesia in patients undergoing elective orthopaedic lower limb surgeries and the quality of analgesia was compared with epidural plain bupivacaine. ^[1] Methods: Ninety ASA physical status classes I-II patients, between 18 to 65 years of age, of either sex, scheduled to undergo laparoscopic cholecystectomy were included in this randomised double blind study. ^[2] In this randomised double blind, repeated measures supplementation study the inflammation stimulus was provided by eccentric exercise and one group was supplemented with ω-3 PUFA (EPA and DHA) and the other with olive oil. ^[3] Materials and Methods: Randomised double blinded study among 50 patients hospitalized for cataract surgery. ^[4]

placebo controlled trial

This document details the planned analyses at 12 months post randomisation for the ACT HIV clinical trial (NCT03092817); ‘a randomised double-blind placebo-controlled trial of adjunctive dexamethasone for the treatment of HIV co-infected adults with tuberculous meningitis (TBM)’. ^[1] Methods: A randomised double-blind placebo-controlled trial was conducted to assess the effect of high dose of vitamin A (VA) and daily zinc versus high dose of VA and daily zinc placebo (6 days per week) during four months among the primary school children. ^[2] STUDY DESIGN This randomised double-blind placebo-controlled trial evaluated the efficacy of an herbal medicine product to reduce the symptoms of nocturnal enuresis. ^[3] Methods Combined data of two parallel randomised double-blind placebo-controlled trials TRUST (Thyroid hormone Replacement for Untreated older adults with Subclinical hypothyroidism – a randomised placebo controlled Trial) and IEMO80+ (the Institute for Evidence-Based Medicine in Old Age 80-plus thyroid trial) were analysed as one-stage individual participant data. ^[4] Methods and analysis We present a protocol for a randomised double-blind placebo-controlled trial comparing co-trimoxazole with placebo treatment in children with recurrent RTIs. ^[5] METHODS We analysed longitudinal data from 207 patients within 5 years of onset of schizophrenia, from the randomised double-blind, placebo-controlled trial of minocycline (BeneMin). ^[6] MATERIALS AND METHODS Randomised double-blind placebo-controlled trial. ^[7] D-dimer was measured in 213 individuals at the start and after 48 months of a randomised double-blind placebo-controlled trial with selenium yeast (200 µg/day) and coenzyme Q10 (200 mg/day) (n = 106) or placebo (n = 107). ^[8] We did a randomised double-blind, placebo-controlled trial at four outpatient clinics in France. ^[9] The strength of our study was that it was a randomised double-blind placebo-controlled trial and it emphatically showed no evidence of a benefit for eplerenone in treating CSCR. ^[10] Method: A cluster randomised double-blind placebo-controlled trial is planned to evaluate the effectiveness of the interventions on preventing malaria infections in soldiers on active duty at Mgambo National Service Camp in Tanga, Tanzania. ^[11] Design Observational sub-study of a single-centre feasibility randomised double-blind placebo-controlled trial. ^[12] STUDY DESIGN A Randomised double blinded placebo controlled trial was performed at a district hospital in New Delhi. ^[13] Regarding the article titled ‘Lycopodium clavatum for the management of urolithiasis: A randomised double blind placebo controlled trial’, we would like to share with you that we could not find the efficacy of Lycopodium in urolithiasis in double-blinded randomised trial, but a positive trend was seen in pain relief. ^[14] We read the publication on ‘Lycopodium clavatum for the management of urolithiasis: A randomised double blind placebo controlled trial’ with a great interest. ^[15]

placebo controlled single

Methods We performed a randomised double-blind placebo-controlled single-centre trial of simvastatin at a daily dose of 40 mg versus placebo in patients with Global Initiative for Chronic Obstructive Lung Disease criteria grades 2–4 at a tertiary care pulmonology department in Austria. ^[1] A randomised double-blind placebo-controlled single ascending dose study was performed with six dose levels of KBP-042 (5, 7. ^[2] A randomised double-blind placebo-controlled single ascending dose study was performed with six dose levels of KBP-042 (5, 7. ^[3]

placebo controlled study

METHODS We conducted a randomised double-blind placebo-controlled study in moderate to severe asthmatic patients (n=44) to investigate the effect of an inhaled corticosteroid (budesonide 400 μg/day) and the combination of budesonide with an oral statin (simvastatin 10 mg/day) given for 8 weeks on autophagy protein expression in sputum cells by using immunocytochemistry and measurement of IL-10 release. ^[1] METHODS We perform a randomised double-blinded two-visit placebo-controlled study with 84 healthy young adults. ^[2]

placebo controlled crossover

Methods The LIONESS trial was a single-centre randomised double-blind placebo-controlled crossover study to determine whether prolonged GLP-1R activation could improve exercise haemodynamics in chronic stable angina patients. ^[1]

Prospective Randomised Double Blind

Methods: This prospective randomised double blind study was conducted in seventy patients aged 18–65 years, American Society of Anesthesiologists grade I-II, scheduled for lower abdominal and lower limb surgery under spinal anaesthesia. ^[1] Methods: 64 parturient of ASA I /II at full term gestation and presenting for Elective Lower Segment Caesarean Section surgery were enrolled and allocated to either of two groups, Group 1:(( Parturient in sitting position during induction of spinal anaesthesia (n=32)) and Group 2(: Parturient in left lateral decubitus position during induction of spinal anaesthesia (n=32)) using computer generated random numbers in this prospective randomised double blind study. ^[2] A prospective randomised double blind study was carried out in 60 patients posted for upper limb orthopaedic surgery. ^[3]

randomised double blind study

SUMMARY: This randomised double blind study was designed to evaluate the analgesic efficacy of bupivacaine with verapamil mixture given through lumbar epidural route for postoperative analgesia in patients undergoing elective orthopaedic lower limb surgeries and the quality of analgesia was compared with epidural plain bupivacaine. ^[1] Methods: This prospective randomised double blind study was conducted in seventy patients aged 18–65 years, American Society of Anesthesiologists grade I-II, scheduled for lower abdominal and lower limb surgery under spinal anaesthesia. ^[2] Methods: Ninety ASA physical status classes I-II patients, between 18 to 65 years of age, of either sex, scheduled to undergo laparoscopic cholecystectomy were included in this randomised double blind study. ^[3] Methods: 64 parturient of ASA I /II at full term gestation and presenting for Elective Lower Segment Caesarean Section surgery were enrolled and allocated to either of two groups, Group 1:(( Parturient in sitting position during induction of spinal anaesthesia (n=32)) and Group 2(: Parturient in left lateral decubitus position during induction of spinal anaesthesia (n=32)) using computer generated random numbers in this prospective randomised double blind study. ^[4] A prospective randomised double blind study was carried out in 60 patients posted for upper limb orthopaedic surgery. ^[5]

randomised double blind placebo

Regarding the article titled ‘Lycopodium clavatum for the management of urolithiasis: A randomised double blind placebo controlled trial’, we would like to share with you that we could not find the efficacy of Lycopodium in urolithiasis in double-blinded randomised trial, but a positive trend was seen in pain relief. ^[1] We read the publication on ‘Lycopodium clavatum for the management of urolithiasis: A randomised double blind placebo controlled trial’ with a great interest. ^[2]