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NCT ID: NCT02785510 Recruiting - Parkinson's Disease Clinical Trials

Determining Clinical Profile of Parkinson's Disease Among Egyptian Population

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

Parkinson's disease is the second most common neurodegenerative disease affecting about 1-3% of population above 60 years. Recently, non-motor symptoms are getting more attention in PD management. The pattern of PD onset and clinical course differ from one population to another. Many studies have been conducted to determine the clinical profile of PD in populations worldwide. However, no similar studies have been conducted in Egypt. Therefore, the investigators will conduct a nation-wide, collaborative, cross sectional study to determine the pattern of Parkinson's disease onset, clinical course, and non-motor symptoms among Egyptian population.

NCT ID: NCT02778802 Recruiting - Clinical trials for Pulmonary Hypertension

Pulmonary Hemodynamics in Patients With Severe Emphysema Pre and Post BLVR

Start date: June 2016
Phase: N/A
Study type: Observational

This study is designed as a prospective study, with the primary endpoint being changes in pulmonary hemodynamic parameters after ELVR in patients with severe emphysema. Secondary endpoints will be changes in lung function parameters, exercise capacity, and QoL.

NCT ID: NCT02778217 Recruiting - Clinical trials for Sub-optimal Culture Conditions

Blastocyst Culture in a Time-lapse Incubator

Start date: May 2016
Phase: N/A
Study type: Interventional

Culture media used to support development of zygotes to the blastocyst stage is based on two basic philosophies: a single step medium "let-the-embryo-choose" or a sequential medium "back-to-nature". For single step media, there are two types of protocol can be used for the culture of human preimplantation embryos: 1. Interrupted single medium culture, in which the medium is renewed on the Day 3 of embryo culture 2. Uninterrupted single embryo culture, in which the same single medium is used throughout the 5-6 days of culture with no replenishment or replacement on Day 3. Investigators aim to compare the blastocyst development and clinical outcome between the two types of protocols of a single medium (with or without renewal on Day 3)

NCT ID: NCT02774928 Recruiting - Clinical trials for Pulmonary Hypertension

Clinical Profile of Patients With Pulmonary Hypertension Due to Lung Diseases ( Single Center Experience)

Start date: June 2016
Phase: N/A
Study type: Observational [Patient Registry]

Development of pulmonary hypertension (PH) in chronic lung diseases has both functional and prognostic implications . PH in Lung diseases is usually mild to moderate with preserved cardiac output, and evolves slowly alongside the progression of lung disease and hypoxemia . However, a minority of patients develop severe PH with elevations in pulmonary artery pressure that have been described as ''out of proportion'' to the underlying disease . The aim of this study is to compare the characteristics and outcomes of consecutive patients with PH-due to lung diseases diagnosed at our specialist referral center over a 1-year period.

NCT ID: NCT02771405 Recruiting - Clinical trials for Hepatocellular Carcinoma

Impact of Interferon Free Regimens in Patients With Chronic HCV and Successfully Treated HCC

FRI-STC
Start date: March 2016
Phase: Phase 3
Study type: Interventional

The study will recruit 150 patients with HCV related HCC ,after HCC treatment the patients will undergo treatment with different regimens of DAAs.

NCT ID: NCT02768376 Recruiting - Clinical trials for Laparoscopic Cholecystectomy

Spinal for Laparoscopic Cholecystectomy

Sp-Lap
Start date: March 2016
Phase: N/A
Study type: Interventional

In this study, the investigators will study spinal anesthesia for laparoscopic cholecystectomy in comparison to general anesthesia (GA) regarding patient satisfaction as a primary variable, intraoperative complications, postoperative analgesic requirements, postoperative nausea and vomiting, patient hospital stay (secondary variables).

NCT ID: NCT02768259 Recruiting - Clinical trials for Pulmonary Hypertension

Prevalence of Pulmonary Arterial Hypertension in Patients With Connective Tissue Diseases in Egyptian Patients

Start date: June 2016
Phase: N/A
Study type: Observational [Patient Registry]

- Measuring the incidence and prevalence of PAH in Egyptian patients with different types of MCD - Determination of survival & the risk factors of mortality.

NCT ID: NCT02766764 Recruiting - Subfertility Clinical Trials

Combined Dehydropeiandrosterone and Growth Hormone in Women With Expected Poor Ovarian Response Undergoing ICSI

Start date: June 2016
Phase: Phase 4
Study type: Interventional

Two hundred and thirty women with expected poor ovarian response undergoing IVF/ICSI will be randomly divided into 2 equal groups using computer generated random numbers. Group 1 will receive DHEA 25 mg (DHEA 25mg, Natrol , USA) t.d.s for 12 weeks before starting IVF/ICSI cycle in addition to Growth hormone (GH; Somatotropin, Sedico, Egypt) 4 IU on day 6 of human menopausal gonadotropin (hMG) stimulation in a daily dose of 2.5 mg subcutaneous (sc) until the day of human chorionic gonadotropin (hCG) triggering Group 2 will receive an oral placebo t.d.s. daily for 12 weeks before ICSI in addition to a sc placebo similar to GH daily from day 6 of stimulation until the day of hCG trigger.

NCT ID: NCT02766504 Recruiting - Clinical trials for General Anesthesia of Morbid Obese Patients

Ultrasound in Airway Assessment of Morbidly Obese Patients

AiUs
Start date: October 2015
Phase: N/A
Study type: Observational

the study aims to evaluate the role of airway ultrasound as a new evolving modality in assessment and management of airway in surgical patients

NCT ID: NCT02765984 Recruiting - Clinical trials for Placenta Implantation Site

Relation of Implantation Site to Placental Site

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

Trans vaginal ultrasound with a partially full bladder will be done at gestational age earlier than 10 weeks to assess the site of intrauterine gestational sac to the endometrial cavity and the distance between the implantation site and the internal cervical os . Doppler assessment of the retrochorionic blood flow at the area behind the maximum chorionic tissue to detect resistance index.