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NCT ID: NCT03182517 Recruiting - Clinical trials for Chronic Kidney Diseases

Parathyroid Hyperplasia in Patients With Chronic Kidney Disease.

Start date: February 1, 2018
Phase:
Study type: Observational

Secondary hyperparathyroidism is an important complication in patient with chronic kidney disease . It is associated with bone complication and an increase in cardiovascular mortality The parathyroid hormone rises in these patients as consequence of low concentration of vitamin D3 ,reduction in quantities of serum calcium, phosphorus retention and reduction of vitamin D receptors sensitive to calcium.

NCT ID: NCT03182114 Recruiting - Clinical trials for Cesarean Section Complications

Supine Versus Left Lateral Tilted Position During Cesarean Delivery

Start date: June 12, 2017
Phase: Phase 4
Study type: Interventional

In this study, we will investigate the effect of left lateral tiling performed after spinal block on maternal hemodynamics compared to ordinary supine position

NCT ID: NCT03181776 Recruiting - Clinical trials for Cesarean Section Complications

Hemodynamic Effect of Left Tilting in Cesarean Delivery

Start date: June 22, 2017
Phase: N/A
Study type: Interventional

The aim of this work is to investigate the effect of different angles of lateral tilt on the maternal hemodynamics before and after subarachnoid block

NCT ID: NCT03180567 Recruiting - Thrombosis Clinical Trials

Pharmacogentic Screening of Coumarine Based Oral Anticoagulant Using Next Generation Seguencer

Start date: June 6, 2017
Phase: N/A
Study type: Interventional

As drug response is a complex trait in the majority of cases using an optimal starting dose for an individual may reduce the time taken to reach a stable INR, and reduce the risk of having either a high INR (with a risk of bleeding) or a low INR (with a risk of thrombosis)

NCT ID: NCT03178500 Recruiting - Polycystic Ovary Clinical Trials

Clomiphene Citrate Stair-Step Protocol

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

A RCT will be conducted to compare the traditional clomiphene citrate regimens for ovulation induction with the stair-step protocol. Sixty women will be included after obtaining their written informed consent and will be randomized into either of the 2 groups.

NCT ID: NCT03177824 Recruiting - Clinical trials for Fetal Growth Restriction

Sildenafil Citrate for Treatment of Growth-restricted Fetuses

Start date: March 30, 2017
Phase: Phase 3
Study type: Interventional

The aim of this study is to assess the effect of Sildenafil citrate therapy on neonatal outcomes in women with fetal growth restriction.

NCT ID: NCT03176992 Recruiting - Clinical trials for Endometrial Hyperplasia

Surgicel® & Endometrial Ablation in the Management of Perimenpausal Heavy Menstrual Bleeding

Start date: June 2015
Phase: Phase 2
Study type: Interventional

Two hundred & forty patients aged from 40 to 50 years - complaining of heavy menstrual bleeding that is unresponsive to hormonal lines of treatment & requesting conservative surgical approach- were randomized into 3 groups; group A (Surgicel group) in which 80 patients underwent formal curettage followed by insertion of 4 pieces of Surgicel inside the uterine cavity, group B (Thermal balloon ablation group) in which 80 patients underwent thermal balloon ablation using bipolar radiofrequency electrical energy (Novasure), group C (Endometrial resection group) in which 80 patients underwent transcervical Hysteroscopic endometrial resection.All patients were followed up over duration of 18 months following the procedure (at 3,6,12 & 18 months). Primary outcome included amenorrhea rates

NCT ID: NCT03176017 Recruiting - Clinical trials for Prostate Hyperplasia

Ejaculatory Sparing Transurethral Incision Of The Prostate (ES-TUIP) Versus Conventional TUIP

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

In this study, Investigators planned to compare ejaculatory sparing and non-ejaculatory sparing (conventional) TUIP using both subjective and objective assessment tools for the degree of deobstruction. Furthermore, the impact of both techniques on ejaculation and its secondary effect on orgasm perception and different domains of sexual function will be thoroughly assessed.

NCT ID: NCT03175393 Recruiting - Clinical trials for Postprandial Dyslipidemia

Relation Between Postprandial Lipogram and Coronary Artery Disease Severity

Start date: July 1, 2017
Phase: N/A
Study type: Observational

Coronary artery disease (CAD) is usually used to refer to the pathological problem affecting the coronary arteries (usually atherosclerosis) that leads to Coronary Heart disease (CHD) which includes the diagnoses of angina pectoris, MI and silent myocardial ischemia. Despite the mortality for this condition has gradually declined over the last decades in western countries, it still causes about one-third of all deaths in people older than 35 years. Dyslipidemia is very important risk factors of atherosclerosis that is one of the causes leading to cardiovascular disease Despite management of dyslipidemia by controling fasting total plasma cholesterol and LDL cholesterol as these are the best biomarkers for prediction of cardiovascular diseases (CVD) risk. LDL elevation is absent in many patients with atherosclerosis and about 1/3 of cardiac events remains to be unpredicted using this method. Even more, in fasting normolipidemic subjects, increased CVD risk is associated with an exaggerated postprandial lipemic response. Postprandial dyslipidemia is defined as a rise in triglyceride-rich lipoproteins (TRLs), including chylomicron remnants (CMRs) and remnant lipoproteins (RLPs), after eating, has drawn an increasing interest recently because of its association with cardiovascular events. Chylomicron remnants (CMRs) have been shown to penetrate the artery wall and to be retained within the intima. Endothelial dysfunction is an initial process of atherogenesis and it contributes to the pathogenesis of CHD. Postprandial hyperlipidemia (postprandial hypertriglyceridemia) is involved in the production of proinflammatory cytokines, recruitment of neutrophils, and generation of oxidative stress, resulting in endothelial dysfunction

NCT ID: NCT03174873 Recruiting - Clinical trials for Infertility of Tubal Origin

Tubal Factor in Unexplained Infertility

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

Ray and colleagues define "unexplained infertility" as failure to achieve pregnancy when the semen analysis is normal, evidence for ovulation is present, and tubal patency has been established. The efficacy of treatment declines with increasing age and duration of infertility Infertility is a disease , defined by the failure to achieve a successful pregnancy after 12 months or more of appropriate, timed unprotected intercourse or therapeutic donor insemination, barber evaluation and treatment may be justified based on medical history and physical findings and is warranted after 6 months for women over age 35 years. In unexplained infertility abnormalities are likely to be present but not detected by current methods including semen analysis in the man, assessment of the state of ovulation, ovulation reserve and patency of uterine tubes in the woman. unexplained infertility is not a rare item of infertility. Approximately 15% of infertility couple will be diagnosed with unexplained infertility after their diagnostic workup Many researches studied the laparoscopic tubal factor like tubo-ovarian relation, tubal kinks and fimbrial pathology. But we need to scope on more tubal factors like fatty mesosalpinx , fimbria ovarica, methylene blue free spill and others