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NCT ID: NCT05941910 Recruiting - Clinical trials for Non-Alcoholic Fatty Liver Disease

The Effect of Coenzyme Q10 on Endothelial, Vascular and Myocardial Function

Start date: April 1, 2023
Phase: Phase 2
Study type: Interventional

Non-alcoholic fatty liver disease (NAFLD) is associated with increased cardiovascular risk. The aim of this study is to investigate the effects of coenzyme Q10 (CoQ10) on endothelial, vascular and myocardial function in patients with NAFLD

NCT ID: NCT05949762 Recruiting - Clinical trials for Acute Myeloid Leukemia

Safety and Efficacy of Venetoclax in Combination With Azacitidine and HA Regimen in the Treatment of AML in the Elderly

Start date: April 1, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

This is a prospective phase II, single-arm clinical study that plans to enroll 45 patients aged 60 years or older with primary AML diagnosed after April 1, 2023.The purpose of this trial is to evaluate the efficacy of Venetoclax in combination with azacitidine and HA regimens in elderly patients aged >60 years with primary acute myeloid leukemia and to provide evidence for optimal selection of clinical treatment regimens.

NCT ID: NCT05955118 Recruiting - Open Angle Glaucoma Clinical Trials

Hydrus Microstent as a Quality of Life Consideration

Start date: April 1, 2023
Phase:
Study type: Observational

The study aims to identify if Hydrus microstent implantation in patients with open angle glaucoma (OAG) at the time of cataract surgery improves quality of life for patients and explore what quality of life factors motivate patients.

NCT ID: NCT05962528 Recruiting - Myopia Clinical Trials

Soft Contact Lens Fitting With Different Sagittal Height

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

To evaluate whether there is a difference in subjective and objective fit of soft lenses with different sagittal height

NCT ID: NCT05965596 Recruiting - Psychological Clinical Trials

Effect of a Psycho-educational Intervention on Psychological Outcomes of Gynecological Cancer Patients

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

This study will be conducted to optimize the quality of care rendered for gynecological cancer patients attending the Gynecological Oncology Unit in El-Shatby University Hospital in Alexandria.As well as to assess the effect of implementing a psychoeducational intervention program among gynecological cancer women on the: 1. Quality of life with its different domains (physical, emotional, social and functional). "as a primary objective" 2. Psychological distress and cancer-specific stress. "as secondary objectives"

NCT ID: NCT05967949 Recruiting - PTCL Clinical Trials

A Retrospective Clinical Study on the First-line Maintenance Treatment of PTCL With Chidamide.

Start date: April 1, 2023
Phase:
Study type: Observational

The efficacy and safety of chidamide in first-line maintenance therapy for PTCL will be assessed through a retrospective case analysis.

NCT ID: NCT05981989 Recruiting - Stroke Clinical Trials

Epidural Electrical Stimulation for Stroke Patients - Improve Motor and Sensory Function and Alleviate Pain

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

This study aims to verify whether epidural electrical stimulation (EES) of the cervical spinal cord can activate muscles of the upper limbs in people with hemiplegia following a stroke.

NCT ID: NCT05983900 Recruiting - Dental Caries Clinical Trials

Clinical Evaluation and Antimicrobial Effect of Papain Based Chemo-mechanical Caries Removal Agents

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

Minimally invasive dentistry continues to gain importance, especially in the treatment of permanent teeth with deep caries lesions and immature roots. Chemo-mechanical caries removal (CMCR) is an alternative to the conventional method and consists of the application of a proteolytic substance that softens carious dentin tissue and facilitates its removal using manual instruments. This method can be employed without the use of local anesthesia or burs, thereby preserving sound dental tissue. The trial aim to assess the clinical performance of Brix 3ooo and Papacarie duo gel as chemo-mechanical caries removal agents (CMCR), their performance in terms of time required for the caries removal, patient subjective pain reaction, their radiographic success and their antimicrobial effect in comparison with Atraumatic Restorative Treatment (ART) hand excavation method for caries removal. The trial will include 108 children with age ranging between 8 and 10 years old who have at least one carious first permanent molar will be randomly divided into three groups. A three-arm randomized clinical trial where test groups, group I, caries removal will be using Brix 3000, and group II Papacarie duo will be used, while the control group hand excavation will be the method of caries removal. Dentin samples of three groups will be taken prior to and following caries removal. The total viable streptococci and lactobacilli count will be determined and expressed as colony forming units per milliliter (CFU). The time required for caries removal with each method will be calculated and the subjective pain reaction following each method will be recorded. After complete caries removal step, it will be followed by restoration with glass ionomer restoration. Patients will be followed up at 3-, 6- and 12-month intervals to determine the clinical success and at 6- and 12- month intervals for the radiographic success rate for each caries removal method.

NCT ID: NCT05985226 Recruiting - Clinical trials for Dental Prosthesis, Implant-Supported

Clinical Evaluation of the Effect of the Scanning Pattern on Complete-arch Implant Scans

strategiesIOS
Start date: April 1, 2023
Phase: N/A
Study type: Interventional

This clinical trial aims to analyze and compare the influence of different scanning strategies (zigzag with conventional scan body, circumferential with conventional scan body, surface blocking with conventional scan body, zigzag with low profile scan body, standard strategy with low profile scan body) on the accuracy of the records obtained for a case of fixed rehabilitation on full-arch dental implants in patients of both sexes, over 18 years of age who will be rehabilitated with fixed prostheses on full-arch implants. The main question it aims to answer is if there will be significant differences in scanning accuracy (trueness and precision) between the different groups of digital impressions compared to the reference model (conventional impression with rigid splinting) and types of scan bodies. The patient will undergo conventional impression-taking (with pastes) to obtain the reference model. Subsequently, digital records will be taken with the intra-oral scanner until completing 15 records per group, out of a total of 6 experimental groups (1.- zigzag with conventional scan body (ZZ-SBL), 2.- circumferential with conventional scan body (C-SBL), 3.- surface blocking with scan conventional body (B-SBL), 4.- zigzag with low profile scan body (ZZ-SBL), 5.- a standard strategy with low profile scan body (STD-SBL), 6.- single pass with low profile scan body ( OP-SBL) These experimental groups will be scanned directly in the patient's mouth, to later be compared with the reference model, called the "master model". Researchers will compare the six different methodologies for taking digital impressions to demonstrate which strategies are more accurate, faster, and require fewer frames.

NCT ID: NCT05985603 Recruiting - Stroke Clinical Trials

Comparison of Mirror Therapy and Modified Constrain Induced Movement Therapy on Risk of Fall, Balance and Gait in Stroke

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

There will be a difference between modified constraint induced movement therapy and Mirror Therapy on lower limb for risk of fall, balance and gait in stroke patients.