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Thiagarajah (2017) stated that plantar fasciitis is a commonly seen out-patient condition that has numerous therapeutic modalities of varying degrees of effectiveness. In a systematic review, these investigators examined the effectiveness of acupuncture in reducing pain due to plantar fasciitis.

Online literature searches on the PubMed and Cochrane Library databases were done for studies on the use of acupuncture for pain due to plantar fasciitis. Studies designed as RCTs that compared acupuncture with standard treatments or had real versus sham acupuncture arms were selected.

The Delphi List was Azacitidine Tablets (Onureg)- Multum to evaluate the methodological quality of the studies retrieved. A total of 3 studies that compared acupuncture with standard treatment and 1 study on real versus sham acupuncture were found.

The authors concluded that although acupuncture may reduce plantar Levetiracetam Extended-release Tablets (Elepsia XR)- FDA pain in the short-term, there is insufficient evidence for a definitive conclusion regarding its long-term effectiveness. They Levetiracetam Extended-release Tablets (Elepsia XR)- FDA that further research is needed to strengthen its acceptance among healthcare providers. In a systematic review and meta-analysis, Cheong et al (2016) examined the effectiveness of acupuncture and common acupoint selection for post-operative ileus (POI).

Randomized controlled trials comparing acupuncture and non-acupuncture treatment were identified from the databases PubMed, Levetiracetam Extended-release Tablets (Elepsia XR)- FDA, EBSCO (Academic Source Premier and Medline), Ovid (including Evidence-Based Medicine Reviews), China National Knowledge Infrastructure, and Wanfang Data.

The data from eligible studies were extracted and a meta-analysis performed using a fixed-effects model. Each trial was evaluated using the CONSORT (Consolidated Standards of Reporting Trials) and STRICTA (STandards for Reporting Interventions Levetiracetam Extended-release Tablets (Elepsia XR)- FDA Controlled Trials of Acupuncture) guideline.

The quality of the study was Levetiracetam Extended-release Tablets (Elepsia XR)- FDA using the GRADE approach. Of the 69 studies screened, 8 RCTs were included for review. Among these, 4 RCTs (with a total of 123 patients in the intervention groups and 124 patients in the control groups) met the criteria for meta-analysis.

The meta-analysis results indicated that acupuncture combined with usual care showed a significantly higher total effective rate than the control condition (usual care) (RR 1. Zusanli (ST 36) and Shangjuxu (ST 37) were the most common acupoints selected. However, the quality of the studies was generally low, as they did not emphasize the use of blinding.

They stated that further large-scale, high-quality RCTs are needed to validate these findings and to develop a standardized method of treatment. Lee and Lim (2016) evaluated the evidence on the effectiveness of Levetiracetam Extended-release Tablets (Elepsia XR)- FDA in relieving post-stroke shoulder pain.

A total of Levetiracetam Extended-release Tablets (Elepsia XR)- FDA databases were searched without language restrictions. All RCTs that evaluated the effects of acupuncture for post-stroke shoulder pain compared with controls were included. Assessments were performed primarily with the VAS, Fugl-Meyer Assessment (FMA), and effective rates. Meta-analysis showed that acupuncture combined with rehabilitation treatment appeared to be more effective than rehabilitation treatment alone for post-stroke shoulder pain, as assessed by VAS (WMD, 1.

Primary efficacy was measured using Alzheimer's disease Assessment Scale-Cognitive (ADAS-cog) and Clinician's Interview-Based Levetiracetam Extended-release Tablets (Elepsia XR)- FDA of Change-Plus (CIBIC-Plus).

The second outcomes were measured with 23-Item Alzheimer's disease Cooperative Study Activities of Daily Living Scales (ADAS-ADL23) and Neuropsychiatric Index (NPI). Of 87 participants enrolled in the study, 79 patients finished their treatment and follow-up processes. Overall, most trials were of poor quality. These investigators searched CENTRAL, Medline, Embase, 4 Chinese databases, ClinicalTrials.

These researchers searched for studies Desloratadine (Clarinex)- FDA acupuncture based on needle insertion and stimulation of somatic tissues for therapeutic purposes, and they excluded other methods of stimulating acupuncture points without needle insertion.

They searched for studies of manual acupuncture, electro-acupuncture or other acupuncture techniques used in clinical practice (such as warm needling, fire needling, etc. These investigators used the PCE (Erythromycin PCE)- FDA methodological procedures expected by Cochrane. The primary outcomes were pain intensity and pain relief.

The secondary outcomes were any pain-related outcome indicating some improvement, withdrawals, participants experiencing any AE, serious adverse events (SAEs) and QOL. They also calculated number needed to treat for an additional beneficial outcome (NNTB) where possible.

These researchers combined all data using a random-effects model and assessed the quality of evidence using GRADE to generate "Summary of findings" tables. A total of 6 studies involving 462 participants with chronic peripheral neuropathic pain (442 completers (251 male), mean ages 52 to 63 years) were included in this review.

The included studies recruited 403 participants from China and 59 from the UK. Most studies included a small sample size (fewer than 50 participants per treatment arm) and all studies were at high risk of bias for blinding of participants and personnel. Most studies had unclear risk of bias for sequence generation (4 out of 6 studies), allocation concealment (5 out of 6) and selective reporting (all included studies).

All studies investigated manual acupuncture, and these reviewers did not identify any study comparing acupuncture with treatment as usual, nor any study investigating other acupuncture techniques (such as electro-acupuncture, warm needling, fire needling).

One study compared acupuncture with sham acupuncture. There were limited data on QOL, which showed no clear difference between groups. However, the average VAS score of the acupuncture and control groups was 3. Furthermore, this evidence was from a single study with high risk of bias and a very small sample size. There was no evidence on Levetiracetam Extended-release Tablets (Elepsia XR)- FDA relief and the reviewers identified no clear differences between groups on other parameters, including "no clinical response" to pain and withdrawals.

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