Search results for "Treatment period"

showing 10 items of 15 documents

Pulsed electromagnetic field therapy in the treatment of pain and other symptoms in fibromyalgia: A randomized controlled study

2018

Low-energy pulsed electromagnetic field (PEMF) therapy has been suggested as a promising therapy to increase microcirculation, which is of great concern in patients with fibromyalgia. This study evaluated the effectiveness of PEMF therapy on the treatment of fibromyalgia. A group of 108 women with fibromyalgia were allocated to a 12-week treatment period with an active Bio-Electro-Magnetic-Energy-Regulation (BEMER) device and a similar treatment period with an inactive device. Each patient received active and sham treatments in a random order. Pain and stiffness were assessed on a visual analog scale (VAS, scale 0-100 mm), and functional status was assessed by the Fibromyalgia Impact Questi…

030203 arthritis & rheumatologyPhysiologybusiness.industryVisual analogue scaleBiophysicsGeneral Medicinemedicine.diseaseTreatment periodlaw.invention03 medical and health sciences0302 clinical medicineRandomized controlled triallawAnesthesiaFibromyalgiaMedicineRadiology Nuclear Medicine and imagingFunctional statusActive treatmentbusinessPulsed electromagnetic field therapy030217 neurology & neurosurgeryAfter treatmentBioelectromagnetics
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The effect of vibration therapy on neck myofascial trigger points: A randomized controlled pilot study

2020

[EN] Background: The purpose of this study was to evaluate the effect of low-frequency self-administered vibration therapy into myofascial trigger points in the upper trapezius and levator scapulae on patients with chronic non-specific neck pain. Methods: Twenty-eight patients with chronic non-specific neck pain were randomly assigned into a vibration group, receiving 10 self-applied sessions of vibration therapy in the upper trapezius and levator scapulae trigger points; or a control group, receiving no intervention. Self-reported neck pain and disability (Neck Disability Index) and pressure pain threshold were assessed at baseline and after the first, fifth and 10th treatment sessions. Fi…

AdultMaleUpper trapeziusmedicine.medical_specialtyPressure painmedicine.medical_treatmentESTADISTICA E INVESTIGACION OPERATIVABiophysicsPilot ProjectsVibration03 medical and health sciences0302 clinical medicineNeck painThreshold of painmedicineHumansDisabled PersonsOrthopedics and Sports MedicineIn patientPROYECTOS DE INGENIERIAPhysical Therapy ModalitiesNeck painNeck PainRehabilitationTrigger pointsbusiness.industryRehabilitationTrigger Points030229 sport sciencesMiddle AgedTreatment periodTreatment OutcomePain thresholdPhysical therapyFemalemedicine.symptombusiness030217 neurology & neurosurgeryNeck Disability IndexClinical Biomechanics
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Surface electrical stimulation of the quadriceps femoris in patients affected by haemophilia A.

2006

Eighteen sessions of surface electrical stimulation was applied to the quadriceps femoris of the left leg of ten male subjects affected by severe haemophilia A, while ten healthy subjects constituted the control group. The isometric strength, the electromyographic activity and the diameter of the rectus femoris were measured in both legs before and after a six-week treatment period. After the treatment, the people affected by haemophilia showed a gain in strength by 13.8% in the stimulated leg and by 17.1% in the non-stimulated one. No changes were detected in the electromyographic activity. On the contrary, the diameter of the rectus femoris of the stimulated leg increased in 24.34%, while…

AdultMalemedicine.medical_specialtyAdolescentHaemophilia AStimulationElectric Stimulation TherapyIsometric exerciseHaemophiliaHemophilia AQuadriceps MusclePhysical medicine and rehabilitationIsometric ContractionmedicineHumansIn patientGenetics (clinical)business.industryHealthy subjectsHematologyGeneral MedicineMiddle Agedmedicine.diseaseTreatment periodAnesthesiaCase-Control StudiesSevere haemophilia AbusinessHaemophilia : the official journal of the World Federation of Hemophilia
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Evaluation of the MGDRx eyebag treatment in young and older subjects with dry eye symptoms

2021

Summary Objectives This study aims to evaluate the relationship between application of the MGDRx thermal eyebag and dry eye signs and symptoms in young and older subjects and to compare the results between the two groups. Methods Thirty young, healthily volunteers between 18 and 31 years of age (23.95 ± 3.94 years) and thirty older subjects between 61 and 90 years of age (77.97 ± 8.11 years) participated in this study. Ocular surface parameters were assessed using the Oculus Keratograph 5 M, following the guidelines of the Tear Film and Ocular Surface Dry Eye Workshop II Diagnostic Methodology report. Only subjects with a positive score on at least one questionnaire and an initial Non-Invas…

Adultmedicine.medical_specialtySigns and symptomsYoung AdultSubjective improvementSurveys and QuestionnairesInternal medicinemedicineHumansTelangiectasiaVolunteerMassagebusiness.industryEyelidsMeibomian GlandsLipidseye diseasesTreatment periodOphthalmologymedicine.anatomical_structureTearsMixed-design analysis of varianceDry Eye Syndromessense organsEyelidmedicine.symptombusinessJournal Français d'Ophtalmologie
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Immediate loading implants: Review of the critical aspects

2018

Purpose. Modern dentistry have witnessed, a rapid and continuing evolution. Concerning the implant-rehabilitation protocols, they have beenEdizioniredefined in order to satisfy patient’s increasing expectations in terms of comfort, aesthetic and shorter treatment period. The purpose of this review is to explore the concept of implant immediate loading and the indications for clinical practice. All the critical aspects that could influence the outcomes of this treatment will also be considered. Materials and methods. Three protocols for implant load timing have been classified: immediate loading implants (ILI); early loading implants (ELI); and conventional loading implants (CLI). Two subc…

Bone densityImplant designbusiness.industryImplant dentistryClinical study designDentistryImplant failureReview030206 dentistryImplant stabilityTreatment periodOsseointegration03 medical and health sciences0302 clinical medicineImmediate loading implantImmediate loadingDentistry (all)MedicineImmediate loading implants; Implant design; Implant stability; Dentistry (all)ImplantImmediate loading implantsbusinessGeneral Dentistry030215 immunology
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Lomitapide: a novel drug for homozygous familial hypercholesterolemia

2014

Lomitapide (Juxtapid® and Lojuxta®; Aegerion Pharmaceuticals, Inc., MA, USA), an orally administered inhibitor of the microsomal triglyceride transfer protein, inhibits the synthesis and secretion of ApoB-containing lipoproteins and, thus, reduces plasma levels of LDL cholesterol (LDL-C). Lomitapide has been approved for the therapy of homozygous familial hypercholesterolemia patients. After a proof-of-concept Phase II trial, lomitapide has been tested in a multinational single-arm, open-label, 78-week, Phase III trial. Lomitapide effectively reduced mean plasma LDL-C levels by 50% from baseline in 23 adults with homozygous familial hypercholesterolemia over a 26-week treatment period and t…

DrugSettore MED/09 - Medicina InternaEndocrinology Diabetes and Metabolismmedia_common.quotation_subjectHoFHapheresiFamilial hypercholesterolemiaPharmacologyMicrosomal triglyceride transfer proteinchemistry.chemical_compoundMedicinemedia_commonLdl cholesterolbiologybusiness.industryPlasma levelsmedicine.diseaseLomitapideLomitapideTreatment periodLomitapide; apheresis; HoFHApheresischemistrybiology.proteinlipids (amino acids peptides and proteins)Cardiology and Cardiovascular MedicinebusinessClinical Lipidology
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Infantile postural asymmetry and osteopathic treatment: a randomized therapeutic trial

2005

The aim of this study was to assess the therapeutic efficacy of osteopathic treatment in infants with postural asymmetry. A randomized clinical trial of efficacy with blinded videoscoring was performed. Sixty-one infants with postural asymmetry aged 6 to 12 weeks (mean 9wks) were recruited. Thirty-two infants (18 males, 14 females) with a gestational age of at least 36 weeks were found to be eligible and randomly assigned to the intervention groups, 16 receiving osteopathic treatment and 16 sham therapy. After a treatment period of 4 weeks the outcome was measured using a standardized scale (4-24 points). With sham therapy, five infants improved (at least 3 points), eight infants were uncha…

Malemedicine.medical_specialtyPediatricsPostureTreatment outcomeSham therapylaw.inventionDevelopmental NeuroscienceRandomized controlled triallawHumansMedicinebusiness.industryInfantGestational agePostural asymmetryNeuromuscular DiseasesManipulation OsteopathicTherapeutic trialTreatment periodTreatment OutcomePediatrics Perinatology and Child HealthPhysical therapyFemaleNeurology (clinical)businessDevelopmental Medicine & Child Neurology
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Treatment of chronic pain associated with bruxism through Myofunctional therapy

2017

<p> </p><p><span> </span>Temporomandibular disorders such as bruxism may cause painful clinical conditions and over time lead to chronic facial pain. A combination of therapeutic strategies that are usually undertaken by dentists and gnathologists to reduce bruxism episodes and consequently pain, are myofunctional therapy, pharmacological treatment, intraoral interventions and behavioural treatments. The aim of this work was to understand if myofuntional therapy alone can be a useful therapy for the reduction of chronic facial pain. 24 patients, 9 male and 15 female, age ranging between 25 and 45, were treated with a myofunctional therapy for 9 month. Each pati…

Myofunctional Therapylcsh:MedicineCase ReportElectromyographylcsh:QM1-695Pharmacological treatmentTonic (physiology)myofunctional theraphyMasseter muscle03 medical and health sciences0302 clinical medicinejaw clenchingmedicineOrthopedics and Sports MedicineMolecular Biologybruxismmedicine.diagnostic_testbusiness.industryElectromyographylcsh:RChronic painMuscle activationlcsh:Human anatomy030206 dentistryCell BiologyElectromyography myofunctional theraphy bruxism jaw clenchingmedicine.diseaseTreatment periodAnesthesiaNeurology (clinical)business030217 neurology & neurosurgery
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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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Response to mepolizumab treatment is sustained across 4-weekly dosing periods

2020

Background Mepolizumab (100 mg delivered s.c. every 4 weeks) is indicated for add-on maintenance treatment for patients with severe eosinophilic asthma. Mepolizumab has been shown to reduce exacerbations and the requirement for daily oral corticosteroids, and improve asthma control and symptoms. However, data on the durability of the response to mepolizumab during dosing periods are limited. The aim of this study was to investigate the efficacy profile in patients with severe eosinophilic asthma over the 4-weekly dosing period for various fixed mepolizumab doses. Methods This was a post hoc analysis of data from the phase IIb/III DREAM study. Patients ≥12 years of age with severe eosinophil…

Pulmonary and Respiratory Medicinemedicine.medical_specialtyExacerbationbusiness.industrylcsh:R2lcsh:MedicineEosinophilic asthma14Original ArticlesPlaceboAsthmaTreatment period03 medical and health sciences0302 clinical medicine030228 respiratory systemInternal medicinePost-hoc analysisMedicineIn patient030212 general & internal medicineDosingbusinessMepolizumabmedicine.drugERJ Open Research
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