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[PDF] Top 20 Homeopathic Individualized Q-Potencies versus Fluoxetine for Moderate to Severe Depression: Double-Blind, Randomized Non-Inferiority Trial

Has 10000 "Homeopathic Individualized Q-Potencies versus Fluoxetine for Moderate to Severe Depression: Double-Blind, Randomized Non-Inferiority Trial" found on our website. Below are the top 20 most common "Homeopathic Individualized Q-Potencies versus Fluoxetine for Moderate to Severe Depression: Double-Blind, Randomized Non-Inferiority Trial".

Homeopathic Individualized Q-Potencies versus Fluoxetine for Moderate to Severe Depression: Double-Blind, Randomized Non-Inferiority Trial

Homeopathic Individualized Q-Potencies versus Fluoxetine for Moderate to Severe Depression: Double-Blind, Randomized Non-Inferiority Trial

... ˚Asberg Depression Rating Scale (MADRS) depression scores, using a non-inferiority test with margin of ...treatment. Non-inferiority of homeopathy was indicated because the upper ... See full document

8

Individualized homeopathic treatment and fluoxetine for moderate to severe depression in peri- and postmenopausal women (HOMDEP-MENOP study): a randomized, double-dummy, double-blind, placebo-controlled trial.

Individualized homeopathic treatment and fluoxetine for moderate to severe depression in peri- and postmenopausal women (HOMDEP-MENOP study): a randomized, double-dummy, double-blind, placebo-controlled trial.

... for fluoxetine and homeopathy, respectively) after a 4-week follow-up; ...for fluoxetine and homeopathy, respectively, after eight weeks of treatment ...due to different ...contribute to ... See full document

24

Eficácia e tolerabilidade da homeopatia e da fluoxetina no tratamento da depressão

Eficácia e tolerabilidade da homeopatia e da fluoxetina no tratamento da depressão

... the non-inferiority and tolerability of individualized homeopathic medicines (Q-potencies) in acute depression, using fluoxetine as active ...with moderate ... See full document

109

Effectiveness of radiation synovectomy with samarium-153 particulate hydroxyapatite in rheumatoid arthritis patients with knee synovitis: a controlled randomized double-blind trial

Effectiveness of radiation synovectomy with samarium-153 particulate hydroxyapatite in rheumatoid arthritis patients with knee synovitis: a controlled randomized double-blind trial

... Each patient underwent IAI guided by fluoroscopy while lying comfortably on their back. The knee was positioned at maximum extension with the needle entry point two centimeters from the upper-lateral angle of the patella ... See full document

8

Randomised controlled double-blind non-inferiority trial of two antivenoms for saw-scaled or carpet viper (Echis ocellatus) envenoming in Nigeria.

Randomised controlled double-blind non-inferiority trial of two antivenoms for saw-scaled or carpet viper (Echis ocellatus) envenoming in Nigeria.

... failure to achieve permanent restoration of blood coagulability within 24 hours of the first ...[6,9]. To exclude recurrent envenoming, 20WBCT was repeated 6 hourly for 48 hours after blood coagulability ... See full document

10

Rev. Bras. Reumatol.  vol.55 número1

Rev. Bras. Reumatol. vol.55 número1

... studies to prove the efficacy and safety of intra- and periarticular corticosteroids, they may also be helpful in the management of lupus ...is to assess the efficacy and safety of intra- and peri- ... See full document

2

Clinics  vol.71 número10

Clinics vol.71 número10

... Despite a similar patient cohort in terms of median age and treatment regimens, the rate of febrile neutropenia among the patients in our population was almost half that reported in pivotal studies. The reasons for this ... See full document

7

Clinics  vol.64 número8

Clinics vol.64 número8

... Biopure to develop a safe and effective HBOC have not met with success to ...continues to work towards FDA ...unfulfilled. To succeed, investigators must overcome scientific barriers, as well ... See full document

11

Trends Psychiatry Psychother.  vol.35 número3

Trends Psychiatry Psychother. vol.35 número3

... Particularly important are the ethical and political- ideological issues that pharmacological control of severe pathological aggression raises in clinical practice and in research with children and adolescents. It ... See full document

9

Braz. j. .  vol.83 número1

Braz. j. . vol.83 número1

... compared to non-resorbable traditional gauze strip ...three to four times per day, are mandatory after the operation to prevent synechiae forma- tion and fluid resorption by the ... See full document

6

Intra-articular morphine versus bupivacaine for knee motion among patients with osteoarthritis: randomized double-blind clinical trial

Intra-articular morphine versus bupivacaine for knee motion among patients with osteoarthritis: randomized double-blind clinical trial

... The study was conducted in a double- blind manner and each patient was randomly assigned to one of two groups. The process of randomization consisted of drawing lots for the procedures, which were ... See full document

5

Rev. Bras. Psiquiatr.  vol.32 número2

Rev. Bras. Psiquiatr. vol.32 número2

... of moderate to severe Alzheimer’s disease, acts as weak non-selective NMDA receptor ...first randomized placebo-controlled clinical trial with memantine adjunctive to ... See full document

3

Ahmad Mourad, John R Perfect

Ahmad Mourad, John R Perfect

... helpful to a successful outcome of treatment with a lower burden of yeasts and less destruction from a persistent, dysregu- lated immune system; (2) identification of new, old, and changing risk factors is ... See full document

7

Rev. Bras. Anestesiol.  vol.62 número6 en v62n6a06

Rev. Bras. Anestesiol. vol.62 número6 en v62n6a06

... prospective, double-blind, randomized, placebo-controlled study comparing intraoperative infiltration of 20 mililiters of bupivacaine (treatment, group B) versus saline (placebo), with ... See full document

5

Braz. oral res.  vol.21 número3

Braz. oral res. vol.21 número3

... molive, Divisão Kolynos do Brasil Ltda., Osasco, SP, Brazil) twice a day for 4 weeks. The patients were recalled once a week over a period of 8 weeks for professional tooth cleaning and were maintained in a supportive ... See full document

6

Rev. Bras. Anestesiol.  vol.66 número6

Rev. Bras. Anestesiol. vol.66 número6

... addition to the neonate Apgar score in the first and fifth minute, need to use vaso- pressor for hypotension treatment, fetal extraction time, and duration of surgery were ... See full document

6

Braz. J. Pharm. Sci.  vol.48 número3

Braz. J. Pharm. Sci. vol.48 número3

... Brazil to treat constipation and encephalic vascular accident, but it has not yet been adequately tested for safety and ...was to evaluate the toxicology and safety of the tincture of ...a ... See full document

8

Randomized pharmacokinetic study comparing subcutaneous and intravenous palonosetron in cancer patients treated with platinum based chemotherapy.

Randomized pharmacokinetic study comparing subcutaneous and intravenous palonosetron in cancer patients treated with platinum based chemotherapy.

... can be established based on our results. Yet, 44% of the patients reported no differences in control of emesis between both routes of administration, while 24% and 32% reported better control with SC and IV palonosetron ... See full document

5

A randomized, non-inferiority study comparing efficacy and safety of a single dose of pegfilgrastim versus daily filgrastim in pediatric patients after autologous peripheral blood stem cell transplant.

A randomized, non-inferiority study comparing efficacy and safety of a single dose of pegfilgrastim versus daily filgrastim in pediatric patients after autologous peripheral blood stem cell transplant.

... prospective, randomized, open label, phase III, non- inferiority study, designed by the working group for supportive care of the Italian Association of Pediatric Hematology Oncology (AIEOP) that was ... See full document

8

Arq. NeuroPsiquiatr.  vol.73 número10 X anp X20150109

Arq. NeuroPsiquiatr. vol.73 número10 X anp X20150109

... Trigeminal neuralgia (TN) patients may develop side effects from centrally acting drugs, have contraindications for neurosurgical procedures, or experience relapse during conventional therapies. OnabotulinumtoxinA ... See full document

8

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