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NCT ID: NCT05479903 Recruiting - Stroke Clinical Trials

Study on the Correlation Between Neurotrophic Factors and the Condition of Stroke Patients

Start date: November 16, 2021
Phase: N/A
Study type: Interventional

Stroke is currently the most common disabling disease, which often leads to impairment of sensory, motor, speech and psychological functions, resulting in a reduced quality of life for patients. Therefore, post-stroke functional rehabilitation, especially the rehabilitation of physical function and psychological condition, is particularly important for patients to rejoin society. Acupuncture can promote the functional recovery of patients and facilitate the rehabilitation of limb function, thus improving the quality of survival of post-stroke patients. Neurotrophic factors are diverse, most of which are mainly derived from neuronal cells in the central nervous system and are involved in a variety of neurological functions such as cell growth, differentiation and plasticity, thus promoting recovery of multiple functions after stroke. Many studies have found that different interventions affect the prognosis of stroke patients differently, e.g., long-term acupuncture increases serum levels of brain-derived neurotrophic factor in stroke patients and also has better outcomes than controls in post-stroke neurological recovery and the development of post-stroke psychiatric disorders. This study investigated the effects of different therapeutic measures on patients' functional recovery and neurotrophic factors by setting up a controlled and blinded trial design, which could not only provide clinical evidence for the effectiveness of relevant therapeutic measures, but also verify the clinical value of certain neurotrophic factors (e.g., predicting outcome, assessing condition, and preventing adverse events).

NCT ID: NCT05479825 Recruiting - Clinical trials for Postoperative Complications

Tubeless Intersegmentectomy Plane Identification With Fluorography

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

Background: We aimed to evaluate the combination of inflation- deflation method and fluorography with the ICG injection in the tubeless minimally invasive segmentectomy (no intubation, VATS or Robotic). Methods: A one- armed, prospective randomized controlled study was designed. The intersegmental plane was not so clear during the tubeless minimally invasive segmentectomy, and the presentation of the plane sometimes cost more time. This study will evaluate consecutive patients with the combination of inflation- deflation method and fluorography with the ICG injection.

NCT ID: NCT05479409 Recruiting - Breast Neoplasms Clinical Trials

Neoadjuvant Radiation in Locally Advanced Breast Cancer

Start date: March 1, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether neoadjuvant radiation therapy is effective in improving local-regional control and to explore predictors of response to treatment in inoperable breast cancer patients after 2-6 courses of neoadjuvant chemotherapy.

NCT ID: NCT05479253 Recruiting - Clinical trials for Artificial Intelligence

AI-assisted Endoscopy Report System In Improving Reporting Quality

Start date: November 1, 2021
Phase: N/A
Study type: Interventional

In this study, we proposed a prospective study about the effectiveness of artificial intelligence system for endoscopy report quality in endoscopists. The subjects would be divided into two groups. For the collected endoscopic videos, group A would complete the endoscopy report with the assistance of the artificial intelligence system. The artificial intelligence assistant system can automatically capture images, prompt abnormal lesions and the parts covered by the examination (the upper gastrointestinal tract is divided into 26 parts). Group B would complete the endoscopy report without special prompts. After a period of forgetting, the two groups switched, that is, group A without AI assistance and group B with AI assistance to complete the endoscopy report. Then, the completeness of the report lesion, the accuracy of the lesion location, the completeness of the lesion and the standard part in the captured images, and so on were compared with or without AI assistance.

NCT ID: NCT05478993 Recruiting - Multiple Myeloma Clinical Trials

Selinexor, Pomalidomide, and Dexamethasone For Multiple Myeloma With CNS Involvement

SPODUMENE
Start date: October 12, 2022
Phase: Phase 2
Study type: Interventional

This is a single-arm, open-label, multicenter, exploratory study initiated by investigator to evaluate the efficacy and safety of Selinexor (S) combined with pomalidomide (P) and dexamethasone (D) in the treatment of multiple myeloma with CNS involvement.

NCT ID: NCT05478473 Recruiting - Melanoma Clinical Trials

Clinical Study of Chidamide Combined With Toripalimab in the Treatment of Advanced Melanoma

Start date: October 27, 2022
Phase: N/A
Study type: Interventional

The study was a single-arm study designed to evaluate the efficacy and safety of Chidamide combined with Toripalimab.

NCT ID: NCT05478421 Recruiting - Jaw Cysts Clinical Trials

Radiographic Bone Volume Alteration After Jaw Cyst Enucleation With Different Bone Grafts

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

For decades, implantology has attracted extensive interest for restoration in patients with the defect of dentition. It has emerged as a very established prosthetic with a 5-year survival rate of 96% . However, defect of dentition resulted from jaw cyst remains an ongoing challenge for subsequent implantation treatment. Since it presents as a larger bone lesion than normal teeth extraction sockets and bone quality and quantity in teeth missing area can significantly impact dental implant failure rates . Jaw cysts are one of the most common diseases occurring in the oral and maxillofacial area, and often cause destructive bone lesions followed by specific clinical features, such as located pain, swelling and loosen teeth. Over the years, enucleation of jaw bone cysts has been the standard method of management of jaw cysts because its conservational protocol to remove the lesion thoroughly and reserve important structures and functions. Unfortunately, management of the residual bony cavity remains as a huge dilemma whether to filing the defect with additional material. Clot formation in the first instance is the conventional option for residual cavity recovery. Iodoform sponges are traditionally used in cysts as stuffing material for inflammation preventative purpose, however, it cannot help with the following bone formation. Without any bone filling material, researches revealed that spontaneous bone healing index can be from 25.85% to 76% and from 43.46% to 81.03% after 6 and 12 months post-operative respectively. These ranged results indicated that spontaneous bone healing is not efficient enough especially for patients with the extraction of relevant teeth who may process a subsequent surgery for implantation. As an alternative to this, bone graft material in the surgery has gained increasing attention. Autogenous bone, artificial bone substitutes and mix of them are widely applied to achieve higher bone regeneration. Thereby an alternative surgical procedure should be considered for patients at risk of missing teeth because of jaw cysts. Whether bone graft material could make a remarkable improvement of bone regeneration after cyst enucleation and would this actually benefit the follow-up implantation? Answers are urged to be delivered. Based on the published data, few studies have yielded in the bone healing comparison of spontaneous bone healing and xenograft in jaw cysts. Besides, with the development of medical radiograph, three-dimensional images have played a more important role in the clinic. Whereas, to our knowledge, most researches had adopted two-dimensional radiograph for measurement, such as panoramic radiographs rather than three dimensions. Therefore, we conducted a prospective study to evaluate the shrinkage rate in cyst patients with different extra xenograft (Bio-Oss and collagen sponge). Cone beam computed tomography (CBCT) and three-dimensional model reconstruction were recommended for radiographic and digital analyzation. In summary, this study was aimed to evaluate bone volume augmentation after jaw cyst enucleation with different bone substitutes filling by CBCT and to analyze other influence factors for bone formation as well.

NCT ID: NCT05478408 Recruiting - Mukbang Clinical Trials

Correlation of Mukbang Video Watching Behavior,Internet Addition and Mental Health Among General Population

Start date: August 15, 2022
Phase:
Study type: Observational

This study will describe the general population's current situation of watching "Mukbang" videos, their mental health status and the level of Internet addiction tendency by means of an online survey, and analyze their correlations. It provides a theoretical basis for promoting healthy psychological development and standardizing management of "Mukbang" videos.

NCT ID: NCT05478395 Recruiting - Mukbang Clinical Trials

Correlation of Mukbang Video Watching Behavior,Internet Addition and Mental Health Among Adolescent and Youth

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

The mental health and Internet addiction problems of adolescents and youth can not be ignored and need to be solved urgently. The behavior of watching "Mukbang" videos may be in a mediating position between the two, and its specific effects and mechanisms are still unclear. Based on the theory of use and satisfaction, this study will further explore the interactive relationship between "Mukbang" and mental health and Internet addiction from the perspective of adolescents and young Internet users. Thereby enriching research paths in related fields and providing theoretical basis for clinical mental health guidance or intervention.

NCT ID: NCT05478356 Recruiting - Myopia Clinical Trials

The Effects of Low-dose Atropine and Orthokeratology in Pediatric Myopia Control

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

Both orthokeratology and atropine eye drops are effective methods for myopia control, but few studies have compared them all together simultaneously. Therefore, the primary aim of the present study was to compare the effect of orthokeratology versus low-dose (0.01% and 0.02%) atropine on the control of myopia progression.