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NCT ID: NCT05595421 Completed - Clinical trials for Obsessive-Compulsive Disorder

Clinical and Electrophysiological Outcomes of tDCS in Patients With Treatment Resistant OCD

Start date: July 10, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to analyze the effectiveness of three different montages of transcranial direct current stimulation (tDCS) in treating treatment-resistant OCD.

NCT ID: NCT05594212 Completed - Clinical trials for Obstructive Sleep Apnea

Abdominal Breathing for Depression, Anxiety, Heart Rate Variability in Obstructive Sleep Apnea Patients

Start date: January 25, 2022
Phase: N/A
Study type: Interventional

The research topic is to explore the effectiveness of abdominal breathing on improving of depression, anxiety, and heart rate variability in obstructive sleep apnea patients with depressive symptoms. This study method adopts an experimental research design and divided into experimental group and control group by random sampling. Experimental group receives abdominal breathing training, whereas control group without receiving abdominal breathing training.

NCT ID: NCT05593913 Completed - Clinical trials for Maculopathy, Age Related

Clinical Evaluation of VeriSee AMD in Screening for Age-Related Macular Degeneration

Start date: January 17, 2022
Phase:
Study type: Observational

An observational study is designed to evaluate the clinical performance of VeriSee AMD for potential age-related macular degeneration (AMD) screening from color fundus photography images. The sensitivity and specificity of VeriSee AMD's automated image analysis for screening AMD will be determined through the comparison with the gold standard, which is the judgment of AMD by the ophthalmologists.

NCT ID: NCT05591807 Completed - Tinnitus Clinical Trials

Investigation to the Mechanism of the Neuroplastic Modulation in Central Auditory Tract

Start date: July 2, 2019
Phase:
Study type: Observational

Tinnitus is the awareness of sound or noise in the absence of acoustic stimulation. No definite therapeutic strategy of tinnitus has been developed yet. The current theory of tinnitus is the plasticity theory of neurophysiology model. Although acupuncture has its role in tinnitus treatment, its actual role still remains to be elucidated. Acupuncture has been proposed to induce the development of neuroplasticity. The aim of this project is to undergo a comprehensive investigation to the central auditory effect and the therapeutic effects of acupuncture in tinnitus. According the results of the preliminary studies, the objective auditory measurement and subjective tinnitus perception will be analyzed in tinnitus patients before and after acupuncture.

NCT ID: NCT05591352 Completed - Skin Condition Clinical Trials

Efficacy Testing of Chenopodium Formosanum Extracts on Skin Beauty

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

To assess Chenopodium formosanum extracts on skin condition improvement

NCT ID: NCT05591313 Completed - Clinical trials for Alzheimer Disease 2 Due to Apoe4 Isoform

Acute Exercise on Neurocognitive Function Among Adults With/Without Generic Risk of AD

Start date: May 17, 2016
Phase: N/A
Study type: Interventional

This study explores the acute exercise effect on neurocognitive function and also its potential moderators in an exercise setting and Apolipoprotein E (APOE) genetic risk.

NCT ID: NCT05590767 Completed - Surgery Clinical Trials

Pupillary Pain Index to Evaluate Interscalene Block and Postoperative Pain in Patients Underwent Shoulder Surgery

Start date: October 27, 2022
Phase:
Study type: Observational

When an individual encounters nociceptive pain stimuli, the pupil dilates in a unique manner known as Pupil reflex dilation (PRD).The degree of pupillary reflex dilatation can be further quantified into an objective parameter, termed the Pupillary pain index (PPI), as a monitoring tool for the balance between nociception and antinociception in surgical patients The motivation for this study is to investigate the feasibility of using pupillometry to assess acute pain after shoulder surgery. The purpose of the study is as follows: (1) Can PDR in patients undergoing general anesthesia be used to assess the analgesic effect of interscalene block? (2) Does PPI at the end of surgical anesthesia in such patients correlate with the first numerical pain scale (NRS) during the recovery room?

NCT ID: NCT05590650 Completed - Chemoradiotherapy Clinical Trials

A Pilot Study of Additional Chinese Formula for Concurrent Chemoradiotherapy in Oral Cavity Cancer Patients

Start date: July 7, 2018
Phase: Phase 1
Study type: Interventional

The goal of this clinical trial is to learn about the clinical efficacy of San-Zhong-Kui-Jian-Tang (SZKJT), a formula of Chinese medicine in head and neck cancer patients receiving concurrent chemoradiotherapy (CCRT) treatments. The main questions it aims to answer are: - Can SZKJT improve the completion rate of CCRT? - Can SZKJT reduce the adverse effects of CCRT? - How SZKJT affect the quality of life in the patients receiving CCRT - How about the safety of using SZKJT in the patients receiving CCRT Participants will be asked to: - take SZKJT for 9 weeks during the whole CCRT course - take questionnaires of quality of life

NCT ID: NCT05589324 Completed - Nerve Injury Clinical Trials

Effects of 3D Printing Writing Assisitive Device on Feasibility in Patients With Nerve Injury

Start date: November 1, 2022
Phase:
Study type: Observational

Injury to the central or peripheral nerves can lead to limited hand function and further affect the ability of writing. The use of assistive devices can assist writing performance. However, the habit of holding the pen and the ability of the individual case will affect the selection of aids and the efficiency of writing. The 3D printing aids can be individually designed and adjusted to different angles and types. There is no criterion for 3D printing aids decision, often using a case-by-case trial subjective way to confirm, matching takes more time. Aim: To compare the applicability and efficiency of different types of 3D-printed writing aids in nerve injury cases, and to explore which factors affect the choice of aids.

NCT ID: NCT05586295 Completed - Fatigue Clinical Trials

Vitamin B Complex Improved Exercise Performance and Anti-fatigue

Start date: March 3, 2021
Phase: N/A
Study type: Interventional

The aim of the present study was to evaluate potential beneficial effects of TTFD® EX PLUS (Prince Pharmaceutical Co., Ltd., Yunlin County, Taiwan) on fatigue and ergogenic functions following physiological challenge. The test used a double-blind crossover design and supplementation for 28 days. 32 male and female 20-30 year-old subjects were divided into two groups in a balanced order according to each individual's initial maximal oxygen uptake and were assigned to receive a placebo with equal gender (non TTFD® EX PLUS with same color/day, n=16, 8 male and 8 female) or TTFD® EX PLUS (600mg/tablet/day, n=16, 8 male and 8 female) every morning. After the intervention, there were 28 days of wash-out, during which time the subjects did not receive further interventions.