Clinical Trials Logo

Filter by:
NCT ID: NCT04664816 Recruiting - Clinical trials for Non-Muscle Invasive Bladder Cancer

Omega-3 Polyunsaturated Fatty Acids and Non-Muscle Invasive Bladder Cancer

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

The investigators hypothesize that omega-3 polyunsaturated fatty acids (n-3 PUFAs) might have a role in prevention of the recurrence of non-muscle invasive bladder cancer (NMIBC). The patients who are suffering from high-risk NMIBC will be randomly allocated into two groups: The first group (n-3 PUFAs group): 55 patients will receive omega-3 plus twice daily for one year after transurethral resection of bladder tumor (TURBT). The second group (Control group): 55 patients will receive placebo twice daily for one year after TURBT. All patients will receive intravesical Bacillus Calmette-Guérin (BCG) immunotherapy and they will be followed up for two years. The chemopreventive effect of n-3 PUFAs on the recurrence of NMIBC after TURBT will be studied via magnetic resonance imaging (MRI), inpatient cystoscopy, histopathological examination and molecular studies of the resected bladder tissues.

NCT ID: NCT04664764 Recruiting - type1diabetes Clinical Trials

Intermediate and Long Acting Insulin Young Children Type 1 Diabetes.

Start date: February 21, 2019
Phase: Phase 4
Study type: Interventional

Background: Achieving glycemic control without risking hypoglycemia imposes a major challenge in the management of toddlers and preschool children with Type 1 diabetes(T1D). Optimal insulin therapy for young children with T1D should provide effective glycemic control while minimizing the risk of hypoglycemia and hyperglycemia. Despite the advantages of the basal-bolus insulin regimens, hypoglycemia still presents a major barrier in achieving desirable glycemic control. Objectives: To compare the effectiveness of insulin degludec to insulin glargine and NPH in toddlers and preschool children with T1D in terms of glycosylated hemoglobin(HbA1C) and frequency of hypoglycemic episodes.

NCT ID: NCT04662138 Recruiting - Hepatitis C Clinical Trials

Safety and Efficacy of Different Antiviral Regimens for Hepatitis C Virus Relapse

Start date: August 24, 2020
Phase:
Study type: Observational

The primary goal of hepatitis C virus (HCV) Direct Acting Antivirals (DAAs) is to achieve undetectable HCV RNA in the blood. A response that should be maintained for at least 12 weeks from completion of therapy. This is called sustained virological response (SVR) which corresponds to cure of HCV infection as risk of later relapse is very small. SVR is important to achieve improvement in liver necroinflammation and fibrosis and to decrease complications of cirrhosis. Failing to achieve SVR after treatment requires another regimen for these experienced patients. Real-world data are always needed to evaluate and improve our practices. Here investigators aim to assess tolerability and efficacy of different regimens used for management of genotype 4 HCV relapse.

NCT ID: NCT04661670 Recruiting - Clinical trials for Temporomandibular Joint Disorders

Occlusal Stabilization Splints Equilibrated by Different Techniques and Their Effect on TMD

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

The objective of the study is to evaluate if occlusal stabilization splints equilibrated by articulating paper will have equivalent effect in comparison to occlusal stabilization splints equilibrated by T-scan regarding the relief of the TMD signs and symptoms

NCT ID: NCT04660773 Recruiting - Clinical trials for Refractory Uremic Pruritis

PHOTOTHERAPY VERSUS PREGABALIN IN TREATMENT OF REFRACTORY UREAMIC PRURITIS

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

Patients will be randomly assigned into 2 groups: 1. Group A: (20 patients) will receive NB UVB phototherapy 3 sessions per week for 2 months. 2. Group B: (20 patients) will receive pregabalin oral therapy (50mg after each dialysis session) for 2 months.

NCT ID: NCT04659642 Recruiting - Hemodynamic Clinical Trials

Attenuation of Airway and Cardiovascular Responses to Extubation in Chronic Smokers

Start date: November 30, 2020
Phase: Early Phase 1
Study type: Interventional

The aim of this blind comparative study was to compare the effects of dexmedetomidine, fentanyl and their combination on airway reflexes and hemodynamic responses to tracheal extubation in Adult chronic male smoking patients scheduled for abdominal surgeries (of average 2-3 hours duration).

NCT ID: NCT04658732 Recruiting - Clinical trials for Sedation for Patients Undergoing Peribulbar Block

A Comparative Study of Oral Gabapentin, Oral Alprazolam and Intravenous Dexmedetomidine on Perioperative Anxiety and Pain During Posterior Segment Eye Surgery Under Peribulbar Block : a Randomized, Double-blind Study.

Start date: December 1, 2020
Phase: Phase 1
Study type: Interventional

We hypothesized that gabapentin when given orally as a premedication in patients who perform posterior segment eye surgery under peribulbar block would provide adequate anxiolysis and arousable sedation as alprazolam and dexmedetomidine with minimal side effects .

NCT ID: NCT04658602 Recruiting - Clinical trials for Molar Incisor Hypomineralization

Restoration of Permanent Molars Affected With (MIH) Using Composite Restorations or Preformed Metal Crowns

Start date: December 2020
Phase: N/A
Study type: Interventional

The aim of this study is to compare clinical outcome of using direct esthetic composite restorations in managing MIH cases and the use of preformed metal crowns.

NCT ID: NCT04657237 Recruiting - Clinical trials for Programmed Cell Death 1

Effect of Anesthesia on Expression of Programmed Death-1 and Programmed Death-1 Ligand in Breast Cancer

Start date: January 2017
Phase: N/A
Study type: Interventional

Surgery is first-line treatment for solid tumors. However, surgical trauma-induced physiologic stress has been demonstrated to facilitate metastasis and recurrence in different types of cancer. It has been reported that the PD-1/PD-L1 pathway could be activated by surgical stress. Hence, we instigate the effect of anesthetic technique on expression of PD1 and PD1 ligand.

NCT ID: NCT04656821 Recruiting - Clinical trials for Erector Spinae Plane Block

Erector Spinae Block Versus Thoracic Paravertebral Block for Acute Thoracic Herpes Zoster

Start date: December 5, 2020
Phase: Phase 4
Study type: Interventional

The aim of this research is to study and compare the efficacy and safety of single injection erector spinae plane block and thoracic paravertebral block in prevention of post herpetic neuralgia in patients with acute thoracic herpes zoster.