Search results for "Randomized Controlled Trial"

showing 10 items of 2199 documents

How Effective and Safe Is Bronchial Thermoplasty in “Real Life” Asthmatics Compared to Those Enrolled in Randomized Clinical Trials?

2016

There is limited information on the efficacy and safety of bronchial thermoplasty (BT) inreal life. We evaluated the outcomes of the randomized clinical trials for BT in severe asthmatics, in whom the exclusion criteria were not strictly controlled. A case series of seven asthmatics (M/F: 4/3; age:54.6±2.9years) is reported. Subjects had a statistically significant improvement in AQLQ (from a mean of3.96±1.1to4.5±1.2and5.5±0.6after 6 and 12 months of treatment;p=0.0007) and in the ACQ score (from2.77±0.8to1.83±1.2and1.5±0.8after 6 and 12 months;p<0.001). In the year after BT, severe exacerbations, salbutamol use, and OCS use were significantly lower compared with the 1-yr pretreatment pe…

Pediatricsmedicine.medical_specialtyPretreatment PeriodArticle SubjectMEDLINElcsh:MedicineSettore MED/10 - Malattie Dell'Apparato RespiratorioGeneral Biochemistry Genetics and Molecular Biologylaw.invention03 medical and health sciences0302 clinical medicineRandomized controlled triallawInternal medicineMedicineIn real life030212 general & internal medicineBronchial ThermoplastyGeneral Immunology and MicrobiologyBronchial thermoplastybusiness.industrylcsh:RGeneral MedicineAsthma030228 respiratory systemClinical StudySalbutamolbusinessmedicine.drugBioMed Research International
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Safety and reactogenicity of a novel DTPa-HBV-IPV combined vaccine given along with commercial Hib vaccines in comparison with separate concomitant a…

2002

Objective. Combination vaccines simplify vaccine administration and have the potential to promote compliance and cost-effectiveness by decreasing the number of injections needed to immunize a child. The objective of this study was to assess the safety and reactogenicity of the diphtheria-tetanus toxoid-acellular pertussis-hepatitis B virus-inactivated polio virus (DTPa-HBV-IPV) vaccine when coadministered with different Haemophilus influenzae type B (Hib) vaccines in comparison with separate, commercially available, control vaccines in a 3-dose primary vaccination series. Methods. An open-label, randomized, parallel-group study in 5318 infants who were 8 to 16 weeks of age at enrollment was…

Pediatricsmedicine.medical_specialtyReactogenicityFeverbusiness.industryIncidence (epidemiology)InfantDiphtheria-Tetanus-acellular Pertussis Vaccineslaw.inventionPoliovirus Vaccine InactivatedRandomized controlled trialHib vaccinelawConjugate vaccineConcomitantPediatrics Perinatology and Child HealthmedicineClinical endpointHumansHepatitis B VaccinesVaccines CombinedAdverse effectbusinessDiphtheria-Tetanus-Pertussis VaccineHaemophilus VaccinesPediatrics
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Effect of Neonatal Outcome Estimates on Decision-Making Preferences of Mothers Facing Preterm Birth

2020

This randomized clinical trial examines the effect of neonatal outcomes on the preferences for expectant German mothers for life-sustaining treatments.

Pediatricsmedicine.medical_specialtybusiness.industryMEDLINEmedicine.diseaseOutcome (game theory)language.human_languagelaw.inventionGerman03 medical and health sciences0302 clinical medicineRandomized controlled trialNeonatal outcomesPremature birthlaw030225 pediatricsPediatrics Perinatology and Child HealthResearch Lettermedicinelanguage030212 general & internal medicinebusinessJAMA Pediatrics
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Effectiveness and safety of dexamphetamine sulfate (Attentin

2021

Abstract Background: Randomized controlled trials have shown that dexamphetamine sulfate (DEX) is efficacious in the treatment of attention-deficit/hyperactivity disorder (ADHD) in children and adolescents; however, data on the effectiveness and safety of DEX in routine practice are scarce. Objective: This study investigated the long-term effectiveness and safety of Attentin® (immediate-release DEX) in children and adolescents with ADHD in routine practice. Methods: ATTENTION was a multicenter, prospective, observational, non-interventional study that enrolled pediatric patients with ADHD (aged 6-17 years) with a clinically inadequate response to previous methylphenidate (MPH) treatment. Pa…

Pediatricsmedicine.medical_specialtydexamphetamineRC435-571Impulsivitylaw.invention03 medical and health sciences0302 clinical medicineRandomized controlled trialchildrenlawRating scale030225 pediatricsmental disordersmedicineClinical endpointADHDPsychology0501 psychology and cognitive sciencesadolescentsPsychiatryMethylphenidatebusiness.industry05 social sciences3. Good healthBF1-990Blood pressureMedicineObservational studyOnset of actionmedicine.symptombusiness050104 developmental & child psychologymedicine.drugScandinavian journal of child and adolescent psychiatry and psychology
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Long-term risk of recurrent venous thromboembolism among patients receiving extended oral anticoagulant therapy for first unprovoked venous thromboem…

2021

Background: The long-term risk for recurrent venous thromboembolism (VTE) during extended anticoagulation for a first unprovoked VTE is uncertain. Objectives: To determine the incidence of recurrent VTE during extended anticoagulation of up to 5 years in patients with a first unprovoked VTE. Methods: MEDLINE, EMBASE, and the Cochrane CENTRAL were searched to identify randomized trials and prospective cohort studies reporting recurrent VTE among patients with a first unprovoked VTE who were to receive anticoagulation for a minimum of six additional months after completing ≥3 months of initial treatment. Unpublished data on number of recurrent VTE and person-years, obtained from authors of in…

Pediatricsmedicine.medical_specialtypulmonary embolismanticoagulant therapy prognosis pulmonary embolism systematic review venous thromboembolism Anticoagulants Humans Prospective Studies Recurrence Risk Factors Pulmonary Embolism Venous Thromboembolismvenous thromboembolismMEDLINE030204 cardiovascular system & hematologylaw.invention03 medical and health sciences0302 clinical medicineanticoagulant therapy; prognosis; pulmonary embolism; systematic review; venous thromboembolism; Anticoagulants; Humans; Prospective Studies; Recurrence; Risk Factors; Pulmonary Embolism; Venous ThromboembolismRandomized controlled trialsystematic reviewRecurrenceRisk FactorslawHumansMedicineProspective Studies030212 general & internal medicinecardiovascular diseasesProspective cohort studyanticoagulant therapybusiness.industryIncidence (epidemiology)AnticoagulantsHematologymedicine.diseaseequipment and supplies3. Good healthPulmonary embolismLong term riskMeta-analysisprognosisbusinessVenous thromboembolismprognosi
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Influence of marginal bone loss on peri-implantitis : systematic review of literature

2019

Background The marginal bone of dental implants is subjected to slight load modifications over time, conditioning implant survival. Objective: Perform a systematic review of the literature analyzing the factors that contribute to marginal bone loss (MBL) and the subsequent development of peri-implantitis. Material and methods Bibliographic research in the databases PubMed, Medline and Scopus between 2010 and 2018 was performed. The inclusion criteria were articles published in the last 10 years and that were in English or Spanish, that were carried out on humans, that were cohort studies, that included cases and controls or that used randomized clinical trials. Exclusion criteria removed ar…

Peri-implantitisbusiness.industrymedicine.medical_treatmentMEDLINEDentistry030206 dentistryReview:CIENCIAS MÉDICAS [UNESCO]law.invention03 medical and health sciences0302 clinical medicineSystematic reviewRandomized controlled triallawUNESCO::CIENCIAS MÉDICASmedicine030212 general & internal medicineImplantOral SurgerybusinessDental implantProspective cohort studyGeneral DentistryCohort study
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Vaginal progesterone decreases preterm birth and neonatal morbidity and mortality in women with a twin gestation and a short cervix: an updated meta‐…

2017

Objective To assess the efficacy of vaginal progesterone for the prevention of preterm birth and neonatal morbidity and mortality in asymptomatic women with a twin gestation and a sonographic short cervix (cervical length ≤ 25 mm) in the mid-trimester. Methods This was an updated systematic review and meta-analysis of individual patient data (IPD) from randomized controlled trials comparing vaginal progesterone with placebo/no treatment in women with a twin gestation and a mid-trimester sonographic cervical length ≤ 25 mm. MEDLINE, EMBASE, POPLINE, CINAHL and LILACS (all from inception to 31 December 2016), the Cochrane Central Register of Controlled Trials, Research Registers of ongoing tr…

Perinatal DeathCervix Uterilaw.inventiontransvaginal ultrasound0302 clinical medicineRandomized controlled trialObstetrics and gynaecologyPregnancylawInfant Mortality030212 general & internal medicineProgesteroneRandomized Controlled Trials as Topic030219 obstetrics & reproductive medicineRadiological and Ultrasound TechnologyObstetricsObstetrics and GynecologyGeneral MedicineMaternal MortalityTreatment OutcomePremature BirthGestationFemalemedicine.symptompreterm deliverymedicine.medical_specialtySystematic ReviewsBirth weightPlaceboAsymptomatic03 medical and health sciencesmedicineHumansRadiology Nuclear Medicine and imagingGynecologyFetusbusiness.industryprematurityInfant NewbornInfantprogestogenscervical lengthAdministration IntravaginalReproductive MedicineprogestinsRelative riskMaternal DeathPregnancy TwinSystematic ReviewbusinessUltrasound in Obstetrics & Gynecology
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Comparative assessment of plaque removal and motivation between a manual toothbrush and an interactive power toothbrush in adolescents with fixed ort…

2019

Introduction The objective of this 2-arm parallel trial was to determine the plaque removal efficacy (main outcome) and the motivation assessment (secondary outcome) comparing a manual versus an interactive power toothbrush in orthodontic patients. Methods Sixty adolescents with fixed orthodontic appliances in both arches were randomized in a 1:1 ratio in this parallel, randomized, examiner-blind controlled clinical trial. Eligibility criteria included at least 16 natural teeth, 1-6 “focus care areas,” plaque score of ≥1.75, no severe caries, gingivitis and periodontitis, no dental prophylaxis, no smoking, no antibiotics, and no chlorhexidine mouth rinse. Subjects were to brush unsupervised…

Periodontitisbusiness.industryDental ProphylaxisChlorhexidineDentistryOrthodontics030206 dentistrymedicine.diseaseSingle CenterDental Plaque Indexlaw.inventionClinical trial03 medical and health sciencesGingivitis0302 clinical medicineRandomized controlled triallawMedicinemedicine.symptombusiness030217 neurology & neurosurgerymedicine.drugAmerican Journal of Orthodontics and Dentofacial Orthopedics
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Effects of timing of adjunctive systemic antibiotics on the clinical outcome of periodontal therapy : a systematic review

2019

Background Many systematic reviews and meta-analysis have indicated beneficial effects of adjunctive systemic antibiotics in periodontal therapy in specific situations. However, some essential issues such as the ideal time of their administration during periodontal therapy remain unanswered. This systematic review aimed to determine at which phase of periodontal treatment would adjunctive systemic antibiotics lead to the best clinical outcomes, during the active phase or in the reevaluation phase. Material and methods Searches in the databases Medline, Scopus and Cochrane Library were conducted. The randomized clinical trials and retrospective cohort studies comparing the clinical benefits …

Periodontitismedicine.medical_specialtyGingival and periodontal pocketbusiness.industryMEDLINERetrospective cohort studyReview030206 dentistryCochrane Librarymedicine.disease:CIENCIAS MÉDICAS [UNESCO]law.invention03 medical and health sciences0302 clinical medicineSystematic reviewRandomized controlled trialClinical attachment losslawUNESCO::CIENCIAS MÉDICASmedicinePeriodontology030212 general & internal medicineIntensive care medicinebusinessGeneral Dentistry
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Healing of intrabony defects following surgical treatment with or without an Er:YAG laser. A pilot study

2004

Aim: The aim of this controlled, parallel design clinical study was to compare the healing of intrabony periodontal defects following treatment with access flap surgery with and without debridement with an Er:YAG laser. Methods: Twenty-three patients each of whom exhibited one deep intrabony defect were randomly treated with either access flap surgery followed by root surface and defect debridement using an Er:YAG laser (KEY3®) (160 mJ, 10 Hz) (test), or with access flap surgery followed by root surface and defect debridement using hand and ultrasonic instruments (control). The following clinical parameters were recorded at baseline and at 6 months: plaque index; gingival index; bleeding on…

Periodontitismedicine.medical_specialtybusiness.industrymedicine.medical_treatmentBleeding on probingDentistrymedicine.diseaselaw.inventionSurgeryRandomized controlled triallawDebridement (dental)medicinePeriodonticsmedicine.symptombusinessProspective cohort studyAdverse effectGingival recessionEr:YAG laserJournal of Clinical Periodontology
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