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Acupuncture clinical trials

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NCT ID: NCT02803736 Not yet recruiting - Breast Cancer Clinical Trials

Effectiveness of Acupuncture for Breast Cancer Related Lymphedema

Acupuncture
Start date: December 2016
Phase: N/A
Study type: Interventional

This multicenter placebo-controlled trial focuses on the efficacy and safety of acupuncture on breast-cancer related lymphedema. 200 participants will be recruited, and randomized in two groups: the real acupuncture group and the sham acupuncture group.

NCT ID: NCT02690389 Completed - Sedation Clinical Trials

Electro-acupuncture and Flumazenil's Effect on Sedation

EA&FLUM
Start date: January 2015
Phase: N/A
Study type: Interventional

Object: To explore the mechanism of the electro-acupuncture (EA) induced sedation effect in general anaesthesia through investigating the role of the Benzodiazepines-GABA system. Method: 80 patients undergoing abdominal surgery were randomly divided into four groups (n=20): C group (propofol only group), F group (propofol + flumazenil group), EA group (propofol + electro-acupuncture group), and EA+F group (propofol + electro-acupuncture + flumazenil group). Before induction, acupuncture needles were inserted at the points of Zusanli (ST 36) and Neiguan (PC 6) bilaterally to elicit"DeQi". Target-controlled infusion (TCI) of propofol was used for the induction and maintenance of anaesthesia. After 15minutes, equilibrium of Narcotrend Index (NT index) was achieved, patients were then assigned to receive different interventions. In EA group and EA+F group, patients received EA for 30 minutes under general anaesthesia, and flumazenil with the dosage of 0.1mg/kg was added in the latter at the end of EA. In C group and F group, patients didn't receive EA, and flumazenil with the dosage of 0.1mg/kg was administered in F Group at the same time point with EA+F group. HR, MAP and NT index were recorded at different time points up to 30 minutes after the end of EA.

NCT ID: NCT02597530 Not yet recruiting - Acupuncture Clinical Trials

Different Stimuli of Transcutaneous Electric Acupoint Stimulation(TEAS) on Acupuncture Anesthesia

TEAS
Start date: November 2015
Phase: N/A
Study type: Interventional

To determine whether treating by transcutaneous electrical acupoint stimulation (TEAS) combined with general anesthetic during peri-operative could alleviate the dosage of anesthetic drugs compared with control and sham group.

NCT ID: NCT02553005 Recruiting - Acupuncture Clinical Trials

Evaluation of the Effect of Acupuncture on Hand Pain, Functional Deficits and Health Related Quality of Life in Patients With Rheumatoid Arthritis

Start date: May 2015
Phase: Phase 0
Study type: Interventional

Rheumatoid Arthritis (RA) is a systemic inflammatory disease characterized by functional disability and pain. Although acupuncture is widely used, western acupuncture studies on RA show no conclusive positive result. Acupuncture is regarded as a reflex therapy, and Traditional Chinese Medicine (TCM) diagnosis was shown to be an individual neurovegetative state allowing to individually allocated acupoints. Positive results were reported using a classical diagnostic procedure to allocate acupoints to the patient according to the Shang Han Lun. The investigators are interested if acupuncture compatible with this ancient theory would be successful in improve hand function in RA patients. The investigators therefore developed a prospective randomized control trial in a three-armed parallel group design with a standardized treatment intervention. Only patients with the TCM diagnosis of a so-called Turning Point syndrome will be allowed in the experimental phase. This may harmonize TCM diagnosis and the standardized intervention, in order to optimize potential therapeutic effects.

NCT ID: NCT02442076 Recruiting - Acupuncture Clinical Trials

Skin and Acupuncture Needle Vibration Behaviors Through Observation

Start date: May 2015
Phase: N/A
Study type: Observational

Skin tremor induced by artery pulses are usually sensed by doctor's fingers in Traditional Chinese Medicine(TCM). On the other hand, vibration of acupuncture needle was also stated by Huang Di Nei Jing (Yellow Emperor). However; the characteristics of skin tremor and its correlation with vibrating acupuncture needles, how the skin tremor and vibration of needles varies from area to area, are not yet clarified.In this study, the abovementioned issues will be investigated experimentally through non-invasive method. About 10 healthy volunteers, aged 20~65, will be recruited. The investigators will measure the needle and the skin tremor by video optical microscopy. The variation of skin tremor and needle vibration and their spectra will be analyzed digitally. The model correlating skin tremor, needle vibration and basic physiological parameters will be constructed.The fact that the skin tremor and the needle vibration come from the same origin is expected. However; due to the leverage effects and different dynamical responses to the source vibrations at different frequencies, needle vibration might exhibit some difference from skin vibration in their power spectra. This study should be able to construct a clear model of the possible vibration sources such as heartbeat and breathing, the area dependence of vibrations, the correlation between the skin and the needle vibrations, and the correlation with other physiological parameters.

NCT ID: NCT02304913 Recruiting - Cancer Clinical Trials

Hypoglossal Acupuncture for Dysgeusia in Patients Undergoing Chemotherapy

OralAcu
Start date: January 2015
Phase: N/A
Study type: Interventional

This randomized controlled trial aims to investigate hypoglossal acupuncture in comparison to sham acupuncture and standard medical treatment (dietary recommendations) in the treatment of dysgeusia in cancer patients undergoing chemotherapy.

NCT ID: NCT01750515 Not yet recruiting - Acupuncture Clinical Trials

Acupuncture as an Adjunctive Treatment for Hepatitis C Patients

Start date: January 2013
Phase: N/A
Study type: Interventional

Objective: to study the effect of Acupuncture on liver cirrhosis, SVR and health related quality of life in HCV patients receiving standard treatment (Peg Interferon+ Ribavirin). Methods: 60 HCV patients receiving standard treatment (Peg Interferon+ Ribavirin) will undergo Serologic screening for hepatitis C virus (Anti-HCV EIAs and/or recombinant immunoblot assay) plus Transient Ultrasound Elastography (FibroScan) to achieve baseline characteristics(17,18,19). Patients will be randomized into intervention and control groups, 30 patients each.In the Intervention group each patient will receive an acupuncture treatment once a week for 12 consecutive weeks(Max 12, Min 8 treatments). Treatment protocol will be individualized for each patient according to TCM diagnosis. This treatment protocol is acceptable and has been published(20,21,22).In the control group patients will receive standard treatment alone, with no other intervention. Data collection: after 12 weeks patients will again undergo Serologic screening for hepatitis C virus (Anti-HCV EIAs and/or recombinant immunoblot assay) plus Transient Ultrasound Elastography (FibroScan) in order to detect changes from baseline and group differences. Inclusion criteria: adult patients with a confirmed HCV infection Exclusion criteria: Under 18 years Can not receive standard Peg interferon+ ribavirin treatment for any reason Psychiatric diagnosis Anaemia of hematologic origin Diabetic patient with uncontrolled diabetes Congestive heart failure, arrhythmia Hepatocellular carcinoma HIV infection Hepatitis B infection Auto immune liver disease or alcoholic liver disease Study duration: 1 year Study Location: "Ziv" medical center, division of liver disease, Israel

NCT ID: NCT01285687 Completed - Post-Operative Pain Clinical Trials

Acupuncture for Post-tonsillectomy Pain Control in Children

Start date: January 2011
Phase: N/A
Study type: Interventional

A randomized, controlled, single-blinded study comparing conventional postoperative analgesia with paracetamol-on-demand with the same regime plus acupuncture. The hypothesis is that postoperative treatment of children undergoing tonsillectomy with acupuncture will reduce pain with minimal unwanted effects.

NCT ID: NCT01283477 Completed - Acupuncture Clinical Trials

Efficacy of Acupuncture for Prophylaxis of Intrathecal Morphine Induced Pruritis in Patients Undergoing Caesarean Delivery

Start date: October 2010
Phase: N/A
Study type: Interventional

Intrathecal morphine is commonly used for pain relief in caesarean delivery. Side effects such as itch (pruritis) and nausea & vomiting are common and have been shown to be the most common cause for dissatisfaction. The incidence of pruritis is 74% even with current available medications. Acupuncture has been shown to be effective for morphine related side effects but has not been evaluated for prophylaxis of itch in pregnant population. PRIMARY OBJECTIVE: Acupuncture at LI 11 reduces the incidence of pruritis after elective caesarean section under spinal with intrathecal morphine

NCT ID: NCT01030029 Completed - Acupuncture Clinical Trials

Auricular Acupuncture in Postoperative Pain

Start date: January 2006
Phase: Phase 4
Study type: Interventional

The effect of acupuncture for postoperative pain control remains controversial. We therefore studied the effects of electrical auricular acupuncture (AA) on postoperative opioid consumption in a randomized, patient-blinded clinical trial. 40 female patients undergoing laparoscopy were included. Anaesthetized patients were randomly assigned to receive AA (shen men, thalamus and one segmental organ-specific point) or electrodes and electrical stimulation for 72 hours. Postoperatively patients received 1 g paracetamol every 6 hours and additional piritramide on demand. A blinded observer obtained the doses of piritramide and the visual analogue pain scores (VAS) at 0, 2, 24, 48, and 72 hours. It was the aim of our study to find out, whether auricular acupuncture reduces postoperative pain.