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NCT ID: NCT05367154 Completed - Myopia Clinical Trials

Factor Analysis of Unintended Initial Dissection of the Posterior Plane

Start date: April 1, 2021
Phase:
Study type: Observational

To explore the potential factors for unintended initial dissection of the posterior plane in a large sample retrospective analysis and surgeons of different levels.

NCT ID: NCT05368376 Completed - Clinical trials for Hypotension Drug-Induced

Is Labetalol More Effective Than Metoprolol for Controlled Hypotensive Anesthesia During Endoscopic Nasal Surgeries?

Start date: April 1, 2021
Phase: Phase 4
Study type: Interventional

Background: Mucosal bleeding is the most frequent complication with endoscopic nasal surgeries, as it interferes with the optimal visualization of the intranasal anatomy, leading to increased complications, operation duration, and blood loss. There are several pharmacological techniques for the appropriate control of intraoperative bleeding. Objectives: To compare the safety and efficacy of oral labetalol versus oral metoprolol as a premedication for controlled hypotensive anesthesia during endoscopic nasal surgeries. Patients and Methods: This is a randomized, double-blind, phase four, comparative clinical trial; carried out on 60 patients, who were candidates for endoscopic nasal surgeries under general anesthesia at our hospital. Patients were randomly allocated into two equal groups; group L, received oral labetalol, and group M, received oral metoprolol.

NCT ID: NCT05371444 Completed - Stroke Clinical Trials

Control of Degrees of Freedom Post-stroke for the Recovery of the Upper Limb

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

The study's methodology will be a single-blind, multicenter, parallel-group randomized controlled trial (RCT). The sample consists of stroke patients (supratentorial ischemic and hemorrhagic stroke of anterior territory) between 18 and 80 years of age, separated into 2 groups of 20 participants. The experimental group called "controlled DoF", the control group 1 called "non controlled DoF". The "controlled DoF" group will use an exoskeleton that will restrict the movement of the trunk and upper limb to release only the joint to work in the plane of interest. The "non-controlled DoF" group will receive the same therapy time as the previous group but without any restriction of joint movements. The training will be functional with multiarticular and combined planes tasks. All groups receive the conventional rehabilitation of the health center (ideally 45 minutes 1 per day). Using motion sensors, clinical scales, and electroencephalography (EEG), the data will be obtained pre-intervention, post-intervention, and in a follow-up at 3 and 6 months.

NCT ID: NCT05409495 Completed - Clinical trials for Platelet-Rich Fibrin

Titanium-prepared Platelet-rich Fibrin in Periodontal Regeneration

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

In this study, the possible effect of blood group distribution on the content of blood biomaterial was investigated. 64 volunteers were included in the study. Various parameters were evaluated. As a result, it was concluded that blood group distribution does not affect blood biomaterial content.

NCT ID: NCT05414435 Completed - Informed Consent Clinical Trials

Informed Consent in Endoscopy: Read, Understood or Merely Signed?

Start date: April 1, 2021
Phase:
Study type: Observational

Informed consent form is a legal document that, ethically, should be obtained before any endoscopic procedure is performed. The main purpose of this research study is to assess the readability, comprehensibility and applicability of the new informed consent proposed by the Portuguese Society of Digestive Endoscopy as a way to standardize the information provided to patients prior to endoscopic exams.

NCT ID: NCT05437042 Completed - Foot Deformities Clinical Trials

Effect of Medial Wedge on Static Balance in Pronated Feet

Start date: April 1, 2021
Phase:
Study type: Observational

The use of heel wedges is often recommended as a clinical routine in individuals with foot pronation. However, there is a lack of information for examining the immediate effect of supports used to restore foot biomechanics on balance. The aim of our study is to examine the immediate effect of calcaneal support in the frontal plane on static balance in individuals with increased pronated foot. In this study, the fore-hind foot load distribution in static bipedal stance will be examined in healthy young adults. Then, static balance measurements will be made on one leg with and without support (medial heel wedge). For the evaluation of static balance on one leg, x-y mean, ellipse surface, A-P index measurements and romberg test will be used. In addition, the pain of individuals will be questioned and their foot postures will be evaluated. Healthy young adult individuals with a subtalar angle of 5 degrees and above in the weighted position will be included in the evaluations. Evaluations of the participants are planned to take approximately 15 minutes.

NCT ID: NCT05444140 Completed - Primary Prevention Clinical Trials

A Feasibility Study of a Health Coaching Programme for Middle-aged Adults With Cardiometabolic Risk

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

Cardiometabolic disease has been an increasing trend globally and remains the major cause of morbidity and mortality. Health coaching, a process of goal-oriented and client-centered partnership that is health-focus and through client enlightenment and empowerment, are generally effective for chronic disease management and prevention of complication. However, there is inconclusive result on the effects of health coaching in the primary prevention of cardiometabolic diseases. Therefore, this study aimed to assess the feasibility and acceptability of a theory-guided health coaching programme for middle-aged adults with cardiometabolic risk.

NCT ID: NCT05465577 Completed - Survivorship Clinical Trials

Coverage and Cost-of-Care (CC) Links- Financial Navigation Program

CC Links
Start date: April 1, 2021
Phase: N/A
Study type: Interventional

This trial is a mixed-methods, non-randomized design guided by the Consolidated Framework for Implementation Research (CFIR) to develop, implement, and evaluate Coverage and Cost-of-Care Links (CC Links) -a novel financial navigation intervention for hematologic cancer survivors and their caregivers.

NCT ID: NCT05476172 Completed - Endometriosis Clinical Trials

The Effect of Dienogest vs. Norethindrone Acetate Treatment in Endometriosis

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

This randomized controlled study aims to investigate the efficiency of medical treatment modalities in endometriosis patients. The study protocol involves two arms. (Dienogest Group and Noretindrone Acetate Group). The patients diagnosed with endometriosis are randomized depending on their protocol ids. The Dienogest group is prescribed 5 mg dienogest per day and neta group is prescribed 5 mg neta per day. The pain scores will be analyzed six months and twelve months after treatment.

NCT ID: NCT05477394 Completed - COVID-19 Clinical Trials

Metabolic Syndrome as Prognostic Factor for Outcome of Sever SARS-COV-2 Cases.

COVID19
Start date: April 1, 2021
Phase:
Study type: Observational

SARS-COV-2 crisis is a severe public health concern in the world. It is now well recognized that older age, diabetes mellitus, obesity (BMI > 30 kg/m2), and hypertension increase the risk of complications and death in SARS-COV-2 patients. This study will describe the spectrum of clinical features, the likely pathophysiologic mechanisms, and potential implications for the management of metabolic syndrome in SARS-COV-2 patients.