Search results for "double-blind method"

showing 10 items of 631 documents

TheMAOA T941G polymorphism and short-term treatment response to mirtazapine and paroxetine in major depression

2006

This study investigated the possible association of the MAOA T941G gene variant with differential antidepressant response to mirtazapine and/or paroxetine in 102 patients with major depression (DSM-IV criteria) participating in a randomized double-blind controlled clinical trial. Female mirtazapine-treated patients homozygous for the T-allele had a significantly faster and better treatment response than TG/GG-patients. In males, we failed to show an association between MAOA T941G gene variant and mirtazapine response. In the paroxetine-treated group, there were no significant differences in treatment response between MAOA T941G genotype groups. Time course of response and antidepressant eff…

AdultMaleOncologymedicine.medical_specialtyTime FactorsGenotypeGenetic LinkageMirtazapineMirtazapineMianserinPolymorphism Single NucleotideCellular and Molecular NeuroscienceDouble-Blind MethodGene FrequencyInternal medicineGenotypemedicineHumansAlleleMonoamine OxidaseGenotypingGenetics (clinical)Depressive Disorder MajorSex Characteristicsbusiness.industryMiddle AgedParoxetineAntidepressive AgentsClinical trialParoxetinePsychiatry and Mental healthTreatment OutcomeEndocrinologyAntidepressantFemalebusinessReuptake inhibitormedicine.drugAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics
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Zolmitriptan inhibits neurogenic inflammation and pain during electrical stimulation in human skin.

2014

Background Triptans are agonists to 5-HT 1B/D/F receptors, which are present on nociceptive neurons not only within but also beyond the trigeminal system. The aim of this study was to investigate whether zolmitriptan interacts with peptidergic nociceptive afferents in human skin. Methods Twenty participants (13 women, median age: 25; interquartile range: 23–26 years) entered the randomized, double-blind, cross-over study. Electrically induced neurogenic flare and pain was assessed after either placebo or zolmitriptan on the ventral thigh. Mechanical pain thresholds were investigated at baseline and after electrical stimulation at the stimulation site. Results The size of the neurogenic flar…

AdultMalePain ThresholdMigraine DisordersPainStimulationZolmitriptanHuman skinTriptansPharmacologyPlaceboYoung AdultDouble-Blind MethodPhysical StimulationmedicineHumansNeurons AfferentOxazolidinonesPain MeasurementSkinNeurogenic inflammationCross-Over Studiesbusiness.industryNociceptorsElectric StimulationTryptaminesSerotonin Receptor AgonistsAnesthesiology and Pain MedicineNociceptionAnesthesiaHyperalgesiaFemalemedicine.symptomNeurogenic Inflammationbusinessmedicine.drugEuropean journal of pain (London, England)
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Activation of the cortical pain network by soft tactile stimulation after injection of sumatriptan.

2006

The anti-migraine drug sumatriptan often induces unpleasant somatosensory side effects, including a dislike of being touched. With a double-blind cross-over design, we studied the effects of sumatriptan and saline on perception (visual analogue scale) and cortical processing (functional magnetic resonance imaging) of tactile stimulation in healthy subjects. Soft brush stroking on the calf (n = 6) was less pleasant (p < 0.04) and evoked less activation of posterior insular cortex in the sumatriptan compared to the saline condition. Soft brushing activated pain processing regions (anterior insular, lateral orbitofrontal, and anterior cingulate cortices, and medial thalamus) only in the sumatr…

AdultMalePain ThresholdPainStimulationSomatosensory systemInsular cortexDouble-Blind MethodPhysical StimulationmedicineImage Processing Computer-AssistedHumansPain MeasurementSkinCerebral CortexBrain MappingSensory stimulation therapyCross-Over Studiesmedicine.diagnostic_testSumatriptanMagnetic Resonance ImagingSerotonin Receptor AgonistsOxygenSumatriptanAnesthesiology and Pain MedicineNociceptionNeurologyTouchNociceptorFemaleNeurology (clinical)Functional magnetic resonance imagingPsychologyNeurosciencemedicine.drugPain
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Short-term effects of kinesio taping in the treatment of latent and active upper trapezius trigger points : two prospective, randomized, sham-control…

2019

Este es el artículo que se ha publicado de forma definitiva en: https://www.nature.com/articles/s41598-019-51146-4 The presence of myofascial trigger points (MTrPs) is one of the most common causes of musculoskeletal problems and may lead to limited professional activity. Among the various treatment methods proposed for MTrPs, Kinesio Taping (KT) is a non-invasive, painless, and less time-consuming method with fewer side efects that has become widely used as a therapeutic tool in a variety of prevention and rehabilitation protocols. The aim of the study was to evaluate the immediate and short-term efcacy of the space correction KT technique in patients with latent or active MTrPs in the upp…

AdultMalePain ThresholdUpper trapeziusmedicine.medical_specialtyAdolescentFisioteràpiaLateral flexionmedicine.medical_treatmentlcsh:MedicineArticleYoung Adult03 medical and health sciences0302 clinical medicineDouble-Blind MethodIntervention TypeSistema musculoesquelético - Heridas y lesiones - Tratamiento.HumansMedicineIn patientProspective StudiesRange of Motion ArticularMyofascial pain syndromes - Treatment.lcsh:ScienceLead (electronics)Myofascial Pain SyndromesNeck PainMultidisciplinaryRehabilitationbusiness.industryVendajes - Uso terapéutico.Rehabilitationlcsh:RTrigger Points030229 sport sciencesSíndrome de dolor miofascial - Tratamiento.Pain managementAthletic TapeCervical VertebraeSuperficial Back MusclesPhysical therapyFemalelcsh:QAnalysis of varianceMusculoskeletal system - Wounds and injuries - Treatment.businessRange of motionBandages and bandaging - Therapeutic use.030217 neurology & neurosurgery
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Randomized, double-blind study comparing percutaneous electrolysis and dry needling for the management of temporomandibular myofascial pain

2018

Background To assess whether the techniques of percutaneous needle electrolysis (PNE) and deep dry needling (DDN) used on trigger points (TrP) of lateral pterygoid muscle (LPM) can significantly reduce pain and improve function in patients with myofascial pain syndrome (MPS) compared to a control group treated with a sham needling procedure (SNP). Material and Methods Sixty patients diagnosed with MPS in the LPM were selected and randomly assigned to one of three groups. The PNE group received electrolysis to the LPM via transcutaneous puncture. The DDN group received a deep puncture to the TrP without the introduction of any substance. In the SNP group, pressure was applied to the skin wit…

AdultMalePercutaneousAdolescentAcupuncture TherapyElectric Stimulation TherapyMyofascial pain syndromeLateral pterygoid muscleElectrolysislaw.inventionDouble blind studyYoung Adult03 medical and health sciences0302 clinical medicineDouble-Blind MethodRandomized controlled triallawHumansMedicineAdverse effectMyofascial Pain SyndromesGeneral DentistryAged030222 orthopedicsDry needlingOral Medicine and Pathologybusiness.industryResearchMyofascial painTrigger PointsPterygoid Muscles030206 dentistryMiddle Aged:CIENCIAS MÉDICAS [UNESCO]medicine.diseaseOtorhinolaryngologyNeedlesSpainAnesthesiaUNESCO::CIENCIAS MÉDICASFemaleSurgerybusinessMedicina Oral Patología Oral y Cirugia Bucal
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Dose escalation vs. continued doses of paroxetine and maprotiline: a prospective study in depressed out-patients with inadequate treatment response

1997

In view of the fact that controlled prospective studies on the benefits of dose escalation of the selective serotonin re-uptake inhibitor (SSRI) paroxetine are lacking, we conducted a double-blind, randomized, parallel-group multicentre study designed to compare the possible benefits of dose escalation of paroxetine and maprotiline in patients suffering from major or minor depression according to modified Research Diagnostic Criteria (RDC) with inadequate treatment response. The study sample consisted of 544 out-patients with different degrees of severity of depression. Patients received either 20 mg paroxetine (n = 271) or 100 mg maprotiline (n = 273) for the first 3 weeks in a double-blin…

AdultMalePersonality InventoryResearch Diagnostic CriteriaDrug Administration Schedulelaw.inventionDouble-Blind MethodRandomized controlled triallawmedicineHumansProspective StudiesMaprotilineProspective cohort studyAdverse effectDepressive DisorderDose-Response Relationship DrugMiddle AgedParoxetineClinical trialParoxetinePsychiatry and Mental healthTreatment OutcomeMaprotilineAnesthesiaAntidepressive Agents Second-GenerationFemaleReuptake inhibitorPsychologymedicine.drugActa Psychiatrica Scandinavica
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Avoidance behaviour: A predictor of the efficacy of pharmacotherapy in panic disorder?

1991

The impact of the avoidance behaviour on the psychopharmacological treatment of panic disorder was explored in the Cross National Collaborative Panic Study (n = 1134 patients); in this double blind randomized trial alprazolam, imipramine and placebo were compared during an 8-week treatment period. Patients with extensive avoidance behaviour (agoraphobia) had the most profit from the active drugs. Counter expectancy these specific drug effects were most pronounced in avoidance behaviour. Active drugs (in particular imipramine) were especially more effective than placebo if the patients presented with associated avoidance behaviour. The results suggest that agoraphobia defines more a particul…

AdultMalePersonality TestsImipraminemedicine.medical_specialtyPlacebobehavioral disciplines and activitiesImipraminelaw.inventionDouble-Blind MethodRandomized controlled triallawmental disordersmedicineHumansPharmacology (medical)Social BehaviorPsychiatryAgoraphobiaBiological PsychiatryAlprazolamPanic disorderPanicFearGeneral Medicinemedicine.diseasePanichumanitiesPsychiatry and Mental healthAlprazolamPanic DisorderFemalemedicine.symptomArousalPsychologyAnxiety disordermedicine.drugAgoraphobiaClinical psychologyEuropean Archives of Psychiatry and Clinical Neuroscience
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Soft tissue cell adhesion to titanium abutments after different cleaning procedures: preliminary results of a randomized clinical trial

2013

Objectives: A randomized controlled trial was performed to assess soft tissue cell adhesion to implant titanium abutments subjected to different cleaning procedures and test if plasma cleaning can enhance cell adhesion at an early healing time. Study Design: Eighteen patients with osseointegrated and submerged implants were included. Before re-opening, 18 abutments were divided in 3 groups corresponding to different clinical conditions with different cleaning processes: no treatment (G1), laboratory customization and cleaning by steam (G2), cleaning by plasma of Argon (G3). Abutments were removed after 1 week and scanning electron microscopy was used to analyze cell adhesion to the abutment…

AdultMalePlasma cleaningGingivaAbutmentDentistrychemistry.chemical_elementOdontologíaOsseointegrationDouble-Blind MethodDental AbutmentsConnective tissue dental abutments randomized controlled trial clinical research glow discharged abutment plasma cleaning.Cell AdhesionHumansProspective StudiesCell adhesionGeneral DentistryAgedTitaniumplasma cleaningChemistrybusiness.industryResearchSterilizationSoft tissueMiddle Aged:CIENCIAS MÉDICAS [UNESCO]Ciencias de la saluddental abutmentsOtorhinolaryngologyclinical researchglow discharged abutmentrandomized controlled trialUNESCO::CIENCIAS MÉDICASFemaleSurgeryImplantConnective tissuebusinessImplantologyTitanium
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Effects of yohimbine on sexual experiences and nocturnal penile tumescence and rigidity in erectile dysfunction.

1996

The therapeutic effect of the alpha 2-antagonist yohimbine in erectile dysfunction was studied in a double-blind placebo-controlled design. Thirty-one male patients underwent extensive clinical, urological, and psychiatric diagnosis and were dichotomically classified into an organic and a nonorganic subgroup. Following a 1-week placebo run-in period, patients were randomly assigned to a placebo or a verum group (yohimbine 15 mg daily) for a treatment period of 7 weeks. The Clinical Global Impression (CGI) scale was used as the primary efficacy parameter. Additionally, nocturnal penile tumescence and rigidity (NPTR) were measured. Global assessment of erectile function applying the CGI scale…

AdultMalePolysomnographyPolysomnographyPlacebolaw.inventionPlacebosAlkaloidsArts and Humanities (miscellaneous)Randomized controlled trialDouble-Blind MethodlawmedicineHumansSexual Dysfunctions PsychologicalGeneral Psychologymedicine.diagnostic_testPenile ErectionTherapeutic effectYohimbineMiddle Agedmedicine.diseaseYohimbineErectile dysfunctionAnesthesiaNocturnal penile tumescenceClinical Global ImpressionPsychologySleepmedicine.drugArchives of sexual behavior
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Posaconazole or Fluconazole for Prophylaxis in Severe Graft-versus-Host Disease

2007

Invasive fungal infections are an important cause of morbidity and mortality after allogeneic hematopoietic stem-cell transplantation.In an international, randomized, double-blind trial, we compared oral posaconazole with oral fluconazole for prophylaxis against invasive fungal infections in patients with graft-versus-host disease (GVHD) who were receiving immunosuppressive therapy. The primary end point was the incidence of proven or probable invasive fungal infections from randomization to day 112 of the fixed treatment period of the study.Of a total of 600 patients, 301 were assigned to posaconazole and 299 to fluconazole. At the end of the fixed 112-day treatment period, posaconazole wa…

AdultMalePosaconazolemedicine.medical_specialtyAntifungal AgentsAdolescentmedicine.medical_treatmentGraft vs Host DiseaseKaplan-Meier EstimateHematopoietic stem cell transplantationOpportunistic InfectionsAspergillosisDouble-Blind MethodRisk FactorsInternal medicinemedicineClinical endpointAspergillosisHumansFluconazoleAgedbusiness.industryIncidence (epidemiology)Hematopoietic Stem Cell TransplantationGeneral MedicineMiddle AgedTriazolesmedicine.diseaseSurgeryTransplantationGraft-versus-host diseaseMycosesFemalebusinessFluconazolemedicine.drugNew England Journal of Medicine
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