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NCT ID: NCT05401890 Not yet recruiting - HCC Clinical Trials

Association Between Serum Ferritin Level and Severity of Liver Disease and Development of HCC in Cirrhotic Patients

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

Association between serum ferritin level and severity of liver disease and development of HCC in cirrhotic patients .

NCT ID: NCT05404087 Not yet recruiting - Breast Cancer Clinical Trials

Evaluation of Contrast Enhanced Breast CT for Diagnosis and Staging of Breast Cancer

CEBCTvsMRI
Start date: August 1, 2022
Phase:
Study type: Observational

Contrast-enhanced breast CT is a novel high resolution and fully 3D imaging method to document abnormalities within the breast. I will establish its value for breast cancer staging and in monitoring therapy response.

NCT ID: NCT05415280 Not yet recruiting - Clinical trials for Psychological Stress

Mindfulness Based Intervention on the COVID-19 Related Distress and Mobile Addiction

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

The interventional study would be conducted to investigate the efficacy of mindfulness based intervention in order to treat psychological stress(anxiety, depression, and stress related COVID-19), and mobile phone addiction during COVID-19 pandemic.

NCT ID: NCT05418920 Not yet recruiting - Esophagitis, Reflux Clinical Trials

Clinical Trial of Reconstruction After Proximal Gastrectomy

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

1) To explore a simple, safe, post-proximal gastrectomy reconstruction method with good absorption and digestive function in order to improve patients' postoperative quality of life; 2) To fill the gap in the comparison of clinical efficacy between left-open single-flap technique and double-flap technique in this specialized field in China; 3) To utilize the experience and foundation of gastrointestinal surgery in the treatment of gastric cancer and integrate the advantageous resources in China; 4) To establish a large-sample, multicenter randomized clinical study in order to promote the establishment and improvement of relevant norms of gastrointestinal reconstruction

NCT ID: NCT05421221 Not yet recruiting - COVID-19 Clinical Trials

Olfactory Training in COVID-19 Associated Loss of Smell

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

Olfactory dysfunction (OD) like hyposmia or anosmia has been realized as a common symptom or even cardinal sign of the disease and can be persisting after recovering. There are two different hypotheses on the pathogenesis of OD in past COVID-19: The central hypothesis, which speculates on neurotrophic abilities on olfactory receptors in the neuroepithelium, and the peripheral hypothesis, which speculates on damage of the sensory olfactory epithelium. Potential treatment strategies aim for the unique neural plasticity of the olfactory system and its potential for recovery. Clinical studies and case reports have shown a promising effect of olfactory training (OT) by frequent sniffing and/or exposure to odors 2-4 times a day for several weeks. The main objective of the study is to assess the effects of olfactory training in patients with COVID-19 related OD on: 1. objective olfactory testing with the Sniffin' sticks test (identification and discrimination) (primary endpoint), 2. subjective OD and its impact on the daily life (key secondary endpoint), 3. other clinical scales and questionnaires referring to OD-related mood and quality of life (other secondary endpoint), 4. gender differences in COVID-19 related OD (exploratory endpoint). Approach / methods OT will be performed twice a day with a 4-odor training set for 12 weeks. Effects of OT on COVID-19 related OD will be measured with objective and subjective efficacy variables. The sense of smell is an important function for social relationships and is therefore a challenging clinical problem with few proven therapeutic options. With this new approach, we want to investigate a possible simple treatment for an impedimental symptom of COVID-19, but also learn more about the pathomechanism of post-infectious OD. To our knowledge, this will be the first study comparing patients with COVID-19 associated OD with and without OT in clinical outcomes.

NCT ID: NCT05423405 Not yet recruiting - Depressive Symptoms Clinical Trials

The Efficacy of Acupressure Therapy on Patient With Depression

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

A new nursing intervention with non-invasive acupressure protocol for activation of parasympathetic nervous system to reduce stress related depression symptoms.

NCT ID: NCT05424653 Not yet recruiting - Clinical trials for Aortic Insufficiency

To Evaluate Safety and Effectiveness of Transcatheter Aortic Valve System in Patients With Severe Aortic Insufficiency

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

To Evaluate the Safety and Effectiveness of Transcatheter Aortic Valve System ( Chengdu Silara Medtech Inc. ,Chengdu, China)in Patients with Severe Symptomatic Aortic Insufficiency

NCT ID: NCT05425368 Not yet recruiting - Deep Caries Clinical Trials

Comparing Two Indirect Pulp Capping Agents for Permanent Teeth

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

Aim of the study: To evaluate clinical and radiographic success rates of silver diamine fluoride versus mineral trioxide aggregate as indirect pulp capping agents in deeply carious young first permanent molars.

NCT ID: NCT05425628 Not yet recruiting - Clinical trials for Cardiovascular Diseases

European FIH Study - NeoChord Transcatheter Mitral Repair System for Symptomatic Mitral Regurgitation

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

Safety and performance evaluation of the NeoChord Transcatheter Mitral Repair System in patients with degenerative mitral valve regurgitation.

NCT ID: NCT05427058 Not yet recruiting - Cervical Cancer Clinical Trials

Hypogastric Plexus Block and Ganglion Impar Block for Cervical and Endometrial Cancer Pain Management

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

This study compared the efficacy and safety of superior hypogastric plexus block and ganglion impar block procedures on the management of pelvic and perineal cancer pain in patients with cervical and endometrial cancer