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NCT ID: NCT03475303 Recruiting - Clinical trials for The Effect of Early Versus Traditional Hospital Discharge for Women Undergoing Elective Cesarean Section

Effect of Early Versus Traditional Hospital Discharge on Maternal Outcome

Start date: March 2018
Phase: N/A
Study type: Interventional

This study will investigate the effect of early hospital discharge versus traditional one on maternal outcome for women undergoing elective cesarean sections. aim of the work is to assess rate of maternal hospital revisits after early hospital discharge at 8-12 hours following elective cesarean delivery compared to the current practice of discharge at 24-48 hours postoperatively.

NCT ID: NCT03471780 Recruiting - Labor Long Clinical Trials

Evaluation of Transperineal US in Labour

Start date: January 8, 2018
Phase:
Study type: Observational [Patient Registry]

Assessment of progress of labour is an important step in decision making of obstetricians

NCT ID: NCT03470064 Recruiting - Tetralogy of Fallot Clinical Trials

Early Right Ventricular Function After Repair Of Tetralogy Of Fallot , An Evidence Based Study.

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

This study aims to assessing right ventricular function early after surgical repair of tetralogy of Fallot and identifying the risk factors associated with development of RV dysfunction.

NCT ID: NCT03469427 Recruiting - Clinical trials for Facial Nerve Paralysis

Multislice Computed Tomography in Cases With Facial Nerve Paralysis Due to Temporal Bone Trauma

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

Facial nerve paralysis is a disfiguring complication which occurs in 7-10 % of temporal bone fractures. The onset of paralysis may be immediate, delayed or undetermined, the latter of which often occurs in unconscious patients with accompanying life-threatening complications.About one fourth has complete paralysis.

NCT ID: NCT03466853 Recruiting - Fetal Malnutrition Clinical Trials

Assessment by the CANS Score Versus Anthropometry and Impact on Early Neonatal Morbidities

Start date: January 3, 2017
Phase: N/A
Study type: Observational

Assessment of malnutrition within 48 hours of birth through anthropometric indices as Weight, Length and Head circumference, Proportionality indices as MAC/HC ratio, Ponderal index and Body mass index, Clinical assessment of nutritional status (CANS) score. Detection of early neonatal morbidities within the first week of life including Hypoglycemia ,Polycythemia, Respiratory Distress Syndrome, Neonatal sepsis, Hyperbilirubinemia and Feeding intolerance

NCT ID: NCT03466840 Recruiting - Alveolar Bone Loss Clinical Trials

Comparison of Coronally Advanced Lingual Flap to Modified MPI for Flap Advancement in Partially Edentulous Patients

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

Comparison of cronally advanced lingual flap to modified periosteal releasing incision (MPRI)

NCT ID: NCT03466632 Recruiting - Colonic Diseases Clinical Trials

Propofol Versus the Use of Dexmedetomidine as a Sedative Agent for Colonosopy

Start date: April 1, 2016
Phase: Phase 3
Study type: Interventional

Dexmedetomidine as a Sedative Agent for Patients Presented for Lower Gastrointestinal Endoscopy

NCT ID: NCT03466619 Recruiting - Clinical trials for Erectile Dysfunction

Penile Prosthesis in Patients With Erectile Dysfunction

Start date: November 1, 2014
Phase: N/A
Study type: Interventional

Erectile dysfunction (ED) is defined as the persistent inability to attain and or maintain an erection sufficient to permit satisfactory sexual performance

NCT ID: NCT03466190 Recruiting - Clinical trials for Mandibular Fractures

Clinical Assessment of Computer-assisted PEEK Versus Conventional Titanium Plates on Mandibular Body Fractures

Start date: August 2, 2017
Phase: N/A
Study type: Interventional

Two groups of patients with mandibular body fractures indicated for Open reduction internal fixation alone or in combination with fractures elsewhere in the mandible or midface. First group will be subjected to traditional titanium internal rigid fixation. Second group will be subjected to custom made PEEK plates.

NCT ID: NCT03465956 Recruiting - Morbid Obesity Clinical Trials

Laparoscopic Sleeve Gastrectomy Short Term Follow up

Start date: April 2018
Phase: N/A
Study type: Interventional

Laparoscopic Sleeve Gastrectomy (LSG), Also known as longitudinal or vertical gastrectomy. LSG was initially considered a first-stage operation in high-risk patients before bilio-pancreatic diversion or Roux-en-Y gastric bypass surgery. However, LSG was subsequently found to be effective as a single procedure for treatment of morbid obesity.LSG functions mainly as a restrictive procedure in which about 75 % of the stomach is removed leaving a narrow gastric tube or sleeve. So, it limits the amount of food that can be eaten at one time via inducing early satiety after eating a small amount of food due to early distension of the fashioned gastric sleeve giving a sense of satiety, consequently losing excess body weight by time.Sleeve gastrectomy may also cause a decrease in appetite by reducing the amount of Ghrelin (hunger hormone) produced by the stomach.