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NCT ID: NCT03757780 Recruiting - Clinical trials for Low; Birthweight, Extremely (999 Grams or Less)

Low Birth Weight Fetuses With Caffeine Use

Start date: November 30, 2018
Phase:
Study type: Observational

Globally, it has been estimated that 15.5% of all infantsare born low birth weight, defined as birthweight less than 2,500 g .

NCT ID: NCT03757286 Recruiting - Maxillary Tumors Clinical Trials

Aesthetic Reconstruction of Onco-surgical Maxillary Defects Using FSF With and Without CAD/CAM Customized Cutting Guide

Start date: July 2019
Phase: N/A
Study type: Interventional

The aim of the study is to compare aesthetic results and operation time of Free Scapular flap with and without CAD/CAM customized osteotomy guide for reconstruction of maxillary Defects.

NCT ID: NCT03757273 Recruiting - Mandibular Tumors Clinical Trials

Aesthetic Reconstruction of Onco-surgical Mandibular Defects Using FFF With and Without CAD/CAM Customized Cutting Guide

Start date: July 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to compare Aesthetic results and operation time of free fibular flap with and without CAD/CAM customized osteotomy guide for reconstruction of mandibular defects.

NCT ID: NCT03757195 Recruiting - Clinical trials for Alveolar Ridge Abnormality of Maxilla

Augmentation of Maxillary Horizontal And Vertical Bone Deficiency Using Mineralized Plasmatic Matrix

Start date: November 15, 2018
Phase: N/A
Study type: Interventional

A new technique of grafting introduce called Mineralized plasmatic matrix. This technique can be used in grafting in anterior zone giving a good results and bone substitution occur using allograft or xenograft. The bone graft have a good consistency when it mixed with plasma give easy application, strength and stability of the graft. Also plasma rich with CGF (Cellular growth factors).

NCT ID: NCT03752554 Recruiting - Resection Cavity Clinical Trials

Assessment of Neurosensory Function Following Segmental Mandibular Resection.

Start date: November 15, 2018
Phase:
Study type: Observational

This study wInclusion criteria for this study will be as follows: - Age group: from 15 to 60 years old. - Patients with with non malignant mandibular neoplasms indicated for segmental resection. Exclusion criteria: - Patients with malignant mandibular neoplasms. All cases will undergo surgery under general anesthesia. The mandibular lesion will be segmentally resected. The cuts will be performed with the aid of the prefabricated digital template. The neurovascular bundle will be separated and protected. Then reconstruction will be performed. Postoperative patient evaluation: Neurosensory examination: Assessment of the inferior alveolar nerve function will be performed preoperatively, 2 and 12 weeks postoperatively through Trigeminal somatosensory evoked potential technique. Six months postoperatively by CBCT for assessment of recurrence

NCT ID: NCT03750370 Recruiting - Varicocelectomy Clinical Trials

Color Doppler in Varicocelectomy in Infertile Patient

Start date: January 1, 2019
Phase:
Study type: Observational

To evaluate the long-term effects of varicocelectomy on testicular arterial flow via Color Doppler Sonography Parameters; The arterial flow velocities (peak systolic velocity [PSV] and end diastolic velocity [EDV]) and the resistance indices against this flow (resistive index [RI] and pulsatility index [PI]) of the testicular artery.

NCT ID: NCT03748043 Recruiting - Iron-deficiency Clinical Trials

the Effectiveness of Lactoferrin in Treatment of Iron Deficiency Anemia in Children With Chronic Tonsillitis

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

the investigators will compare the response to iron deficiency anemia to lactoferrin plus ferrous poly maltose versus ferrous poly maltose in Children With Chronic Tonsillitis

NCT ID: NCT03743727 Recruiting - Clinical trials for Hepatitis C Genotype 4

Treatment of Egyptian Hepatitis C Genotype 4 Infected Children and Adolescents With Combined Ledipasvir/Sofosbuvir

Start date: August 1, 2018
Phase: Phase 4
Study type: Interventional

This is an open, uncontrolled study of twenty-five chronic HCV infected patients carried out at Yassin Abdel Ghaffar Charity Center for Liver Disease and Research. The aim of this study is to investigate the safety & efficacy of combined therapy ledipasvir (LDV) and sofosbuvir (SOF) for treating HCV Genotype 4 in children aged 8 to 18. Due to previous positive results in other clinical studies of this drug it is expected that the drug will have high safety and high efficacy. Safety will be measured by checking for adverse effects, while efficacy will be measured by Real-Time Quantitative Polymerase Chain Reaction (qPCR) detecting viral nucleic acids in blood samples.

NCT ID: NCT03741257 Recruiting - Clinical trials for Intestinal Obstruction Fluid Management With Hypertonic Saline

Comparison Between Two Concentration of Hypertonic Saline in Intestinal Obstruction Surgery

Start date: November 1, 2018
Phase: N/A
Study type: Interventional

Background and Rationale : Perioperative fluid management is a challenging issue in surgical care especially in a procedure specific model. Recently hypertonic saline (HS) has the advantage of using the patient's own total body water by drawing interstitial space. Although it still controversial whether HS is associated with benefits in specific patient populations, particularly with respect to site of lesion and illness severity; these data provide insight into therapeutic modalities to curtail ileus formation. Objectives : - Measurement of total volume of fluid infused, the need of inotropic or vasopressor to maintain adequate hemodynamic parameters with assessment of electrolyte disturbances and S.lactate - The incidence rate of surgical complications; infection and anastomotic dehiscence Study population & Sample size : There were no previous trials comparing the two studied groups of the current trial. We expected a small standardized effect size of 0.2. Based on this effect size, 25 subjects will be needed to elicit the difference between the two groups at an alpha level of 0.05 and power of 0.9 (Whitehead et al; 2016).

NCT ID: NCT03741114 Recruiting - Placenta Previa Clinical Trials

Foley's Catheter Balloon Plus Tranexamic Acid During Cesarean Delivery for Placenta Previa

Start date: December 1, 2018
Phase: N/A
Study type: Interventional

Placenta previa (PP) is an obstetric condition that is closely linked with massive obstetric hemorrhage with a varied incidence about once in every 150-250 live births. Insertion of intrauterine balloon tamponade has been suggested in the management of massive postpartum hemorrhage (PPH). The Bakri balloon has a sausage-like spindle shape and a drainage lumen and is made of silicon. It has been used in cases of uterine atony and placenta previa with a success rate of 90%. However, Bakri balloon is not available in all countries. The aim of this study is to evaluate the efficacy of the use of intrauterine inflated Foley's catheter balloon with or without intravenous tranexamic acid to control PPH during cesarean delivery in cases of placenta previa.