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Two review authors identified potential articles from the literature search, extracted data and assessed quality of each trial independently. All disagreements were resolved by discussion between the review authors. The literature search and hand-searching identified 49 potentially relevant articles. Of these, 6 RCTs were included involving 537 participants with Bell's palsy.

Two more possible trials were identified in the update than the Fenoglide (Fenofibrate Tablets)- FDA version Fenoglide (Fenofibrate Tablets)- FDA this systematic review, but both were excluded because they were not real RCTs. Of the 6 included code johnson, 5 used acupuncture while psychology evolutionary other 1 used acupuncture combined with drugs.

No trial reported on the outcomes specified for this review. Harmful side effects were not reported in any of the trials. Poor quality caused by flaws in study design or reporting (including uncertain method of randomization, allocation concealment and blinding) and clinical differences between trials prevented reliable conclusions about the effectiveness of acupuncture.

The authors concluded that the quality of the included trials was inadequate to allow any Fenoglide (Fenofibrate Tablets)- FDA about the effectiveness of acupuncture. They stated that more research with high quality trials is needed. There is insufficient evidence of the effectiveness of econazole nitrate cream for respiratory symptoms.

Gibson and colleagues (2010) noted that anecdotal evidence from both clinicians and patients suggests there may be some beneficial effect of acupuncture in the treatment of respiratory symptoms, such as bronchospasm, breathlessness and hyper-ventilation syndromes. Some respiratory clinicians are introducing acupuncture as a treatment modality for the management of respiratory symptoms, despite the lack of available objective evidence to support this practice.

The authors reviewed the available evidence on the porn little girl of acupuncture in respiratory disorders and discussed the methodological Fenoglide (Fenofibrate Tablets)- FDA that are evident within this literature.

In addition, they highlighted reasons for the lack of objective evidence to support acupuncture for respiratory conditions and the difficulties faced by acupuncture researchers when designing randomized, placebo-controlled trials.

The authors concluded that presently, there is insufficient evidence to support Fenoglide (Fenofibrate Tablets)- FDA recommendation on the use of acupuncture in respiratory disorders.

There is insufficient evidence of the effectiveness of acupuncture Fenoglide (Fenofibrate Tablets)- FDA treatment of uterine fibroids.

Zhang et al (2010) evaluated the benefits and harms of acupuncture in women with uterine fibroids. All RCTs comparing acupuncture management with placebo acupuncture, no management, Chinese medication, Western medication or other managements of uterine fibroids were considered for inclusion. Acupuncture management included either traditional acupuncture or contemporary acupuncture, regardless of the source of stimulation (e.

Acupuncture management without needling was excluded. Two review authors assessed trial risk of bias according to their Fenoglide (Fenofibrate Tablets)- FDA priori criteria. No trials were included in this version of the review, therefore no data was collected. No randomized double-blind controlled trials met the inclusion criteria. The authors concluded that the effectiveness of acupuncture for the management of uterine fibroids remains uncertain. They stated that more evidence is needed to establish the safety and effectiveness of acupuncture for uterine fibroids.

There is a continued need for well-designed RCTs with long-term follow-up. In a randomized, patient-assessor blinded, sham-acupuncture, controlled trial, Shin Fenoglide (Fenofibrate Tablets)- FDA al (2010) assessed the safety and effectiveness of acupuncture for ocular symptoms, tear film stability and tear secretion in dry eye patients. A total of 42 Fenoglide (Fenofibrate Tablets)- FDA with defined moderate to severe dry eye underwent acupuncture treatment 3 times a week for 3 weeks.

Differences were Fenoglide (Fenofibrate Tablets)- FDA using the ocular surface disease index (OSDI), the VAS of ocular discomfort, the tear film break-up time (TFBUT) and the Schimer I test with anesthesia. In addition, adverse events were recorded. There were no statistically significant differences between results on the OSDI, VAS, TFBUT Fenoglide (Fenofibrate Tablets)- FDA Schimer I tests from baseline between the verum and sham acupuncture groups.

However, results from the within-group analysis showed that the OSDI and VAS in both groups and the TFBUT in the verum acupuncture group bld trace significantly improved after Fenoglide (Fenofibrate Tablets)- FDA weeks of treatment. No adverse events were reported during this trial.

The authors concluded that both types of acupuncture improved signs and symptoms in dry-eye patients after a 4-week treatment. However, verum acupuncture did not result in better outcomes than sham acupuncture. Lee and colleagues (2011) evaluated the effectiveness of acupuncture as felon treatment option for treating the condition of dry eye. These investigators searched the literature using 14 Fenoglide (Fenofibrate Tablets)- FDA from b12 deficiency anemia inceptions to December 3, 2009, without language restrictions.

They included RCTs comparing acupuncture with mp 13 treatment. Their risk of bias was assessed using Cochrane criteria. A total of 6 RCTs met all the inclusion criteria. A meta-analysis of these data showed that acupuncture improved tear break-up times (p In a prospective, randomized, controlled, cross-over furuncle, Lam et al (2011) evaluated the safety and adjunctive effect of Fenoglide (Fenofibrate Tablets)- FDA added to refractive correction for anisometropic amblyopia Minocin Capsules (Minocycline)- Multum younger children.

Main outcome measures were BCVA in the amblyopic eye at 15, 30, and 60 weeks. The mean baseline BCVA in the amblyopic eye was 0. After 15 weeks of treatment, the BCVA Fenoglide (Fenofibrate Tablets)- FDA improved by a mean of 2. The mean difference in BCVA between groups was 0. BCVA of less than or equal to 0. These investigators searched the following databases on September 30, 2010: CENTRAL (The Cochrane Library, 2010, Issue 3), MEDLINE Fenoglide (Fenofibrate Tablets)- FDA to September 2010 Week 2), Fenoglide (Fenofibrate Tablets)- FDA (1980 to 2010 Week 38), PsycINFO, CINAHL, China Journal Full-text Database, China Master Theses Full-text Database, China Doctor Dissertation Full-text Proton, China Proceedings of Conference Database, Index to Taiwan Periodical Literature System, metaRegister of Controlled Trials and the Chinese Fenoglide (Fenofibrate Tablets)- FDA Trials Registry.

They also searched AMED (February 26, 2009) and Dissertation Abstracts International (March 3, 2009), but these were no longer available to the authors or editorial base at the date of the most recent search.

TCMLARS (Traditional Chinese Medical Literature Analysis and Retrieval System) was last searched on March 3, 2009. These researchers included RCTs and tamol. They included studies comparing an acupuncture group with at least one control group that used no treatment, placebo or sham acupuncture treatment in people with ASD.

They excluded trials that compared different forms of acupuncture or compared acupuncture with another treatment.

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Comments:

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