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NCT ID: NCT04996043 Completed - Skin Condition Clinical Trials

Efficacy Testing of Collagen Peptide Drink

Start date: May 17, 2021
Phase: N/A
Study type: Interventional

To assess Collagen Peptide Drink on skin condition improvement

NCT ID: NCT04995328 Completed - Clinical trials for Radiation Dermatitis

Clinical Investigation on the Treatment of Radiation Induced Dermatitis With Radiation Care® Gel

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

The radiotherapy after surgery reduces the risk of recurrence and death is widely used for standard treatment for cancer including breast cancer and head and neck cancer. However, radiation dermatitis is a common side effect and major adverse event of radiotherapy. Radiation induces skin inflammation resulting in redness, itchiness and peeling skin. Radiation dermatitis may be acute or chronic. Acute skin changes occur within 90 days of initiating therapy due to inflammation and DNA damage and chronic skin changes may occur after several weeks or years. Radiation-irritated skin is a treatment-induced symptom caused by radiation dose-limiting toxicity. It damages skin structure and causes a variety of symptoms of cuticle thinning, reducing of collagen in subcutaneous, sweat glands damage, sebaceous glands damage and basal membrane damage. These conditions lead patients to lost work productivity, wound care costs, social isolation, altered body image and affect a patient's quality of life and mental health both during and after treatment and even interrupts the treatment schedule. The treatment of radiation dermatitis is an essential component of radiotherapy. The common treatment includes agents and other dressing products, such as corticosteroid cream, hyaluronic acid, aloe and sucralfate, which are used to prevent or reduce severity of dermatitis. But there is no clear therapeutic or nursing guideline supporting continuous treatment of radiation dermatitis by topical agents currently. In this study, Radiation Care® gel which contain Japanese honeysuckle extract will be used in breast and head and neck cancer patients to test the safety and efficacy to prevent radiation dermatitis and alleviate their radiation-irritated skin symptoms. The primary objective of this study is to evaluate the clinical outcomes of "Radiation Care" gel application in breast cancer and head and neck cancer patients who have radiation dermatitis or radiation-irritated skin due to the radiotherapy.

NCT ID: NCT04993300 Completed - Depression, Anxiety Clinical Trials

Repetitive Transcranial Magnetic Stimulation in Amphetamine Addiction

Start date: February 17, 2022
Phase: N/A
Study type: Interventional

The study aims to test whether transcranial magnetic stimulation (TMS) improves the craving, depression, anxiety and cognitive function during the abstinent period of methamphetamine users.

NCT ID: NCT04990154 Completed - Exercise Clinical Trials

Effects of Intradialytic Exercise on Health-related Quality of Life

Start date: May 25, 2019
Phase: N/A
Study type: Interventional

This study aimed to evaluate the effects of intradialyic exercise on dialytic parameters, HRQL, and depression status in hemodialysis patients. A randomized controlled trial was conducted. Sixty-four participants were recruited using stratified random sampling and allocated with a 1:1 randomization ratio to either experimental group (EG, treated in odd weekdays, n = 32) or comparison group (CG, treated in even weekdays, n = 32). The EG received a 12-week intradialytic exercise, while the CG maintained usual lifestyles. Dialytic parameters, HRQL, and depression status were collected at baseline and at 12 weeks. The results indicated that there were no differences in changes of dialytic parameters from baseline between EG and CG. However, the EG had increased HRQL and reduced depression status at 12 weeks compared with the CG. A 12-week intradialytic exercise is safe, feasible and effective in improved HRQL and reduced depression status for hemodialysis patients.

NCT ID: NCT04989569 Completed - Sepsis Clinical Trials

Serial Body Composition Change for Risk Prediction and Nutritional Guide in Treating Patients With Sepsis

Start date: August 1, 2020
Phase: N/A
Study type: Interventional

To explore whether serial changes of data in body composition of patients with sepsis can help clinician to monitor prognosis.

NCT ID: NCT04987190 Completed - Clinical trials for Cleft Lip and Palate

Progression of Grafted Bone Density in Cleft Alveolus

CDAABG
Start date: January 25, 2021
Phase:
Study type: Observational

The patients with unilateral and bilateral cleft lip and palate received alveolar bone graft surgery. Two time points of cone beam CT were taken for all the patients: post-operative 6 months, and post-operative 2 years. All the CT images were reviewed for the analysis of grafted bone density.

NCT ID: NCT04986202 Completed - Clinical trials for Heart Failure With Preserved Ejection Fraction

Study to Evaluate the Efficacy and Safety of AZD4831 in Participants With Heart Failure With Left Ventricular Ejection Fraction > 40%

ENDEAVOR
Start date: June 30, 2021
Phase: Phase 2/Phase 3
Study type: Interventional

This is a randomised, double-blind, placebo-controlled, multi-center sequential phase 2b and Phase 3 study to evaluate the efficacy and safety of AZD4831 administered for up to 48 Weeks in participants with heart failure with left ventricular ejection fraction > 40%. The study will consist of 2 separate parts, Part A and Part B, approximately 660 participants will be randomised in Part A, 820 in Part B.

NCT ID: NCT04984694 Completed - Quality of Life Clinical Trials

Computerized Virtual Reality in Elderly

Start date: February 3, 2017
Phase: N/A
Study type: Interventional

The number of dementia patients increased with aging population. People with subjective memory complaints or mild cognitive impairment (MCI) may have a high risk of developing dementia. Cognitive /memory training programs have shown the potential positive effects for improving or maintaining the cognitive progression. However, the impact of those cognitive progressions on functional ability and quality of life is not well understood. In addition, it appears to have large variability responsiveness among trained subjects. Most studies did not examine the individual difference associated with training. The major aim will evaluate the cognitive training programs on functional ability and quality of life in older adults. The results will be expected to understand the effectiveness of the computerized virtual reality training, improving or maintaining cognition, physical and psychosocial function, enhancing quality of life, and reducing the risk of developing disability even conversion into dementia in later life.

NCT ID: NCT04983004 Completed - Stroke Clinical Trials

Effectiveness of Tele-rehabilitation Apply to Stroke Inpatient

Start date: August 20, 2021
Phase: N/A
Study type: Interventional

Our study is aimed to explore the differences in effects on the motor function and general condition after telerehabilitation for inpatients with stroke.

NCT ID: NCT04982185 Completed - Thyroid Surgery Clinical Trials

Neuromuscular Block Monitoring During Monitored Thyroidectomy

Start date: August 1, 2019
Phase:
Study type: Observational

Titration of neuromuscular block (NMB) plays a key role in intraoperative recurrent laryngeal nerve monitoring during thyroid surgery. Aim to titrate sugammadex dose based on neuromuscular block degree as a surgeon friendly protocol with high intraoperative neuromonitoring (IONM) quality.