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NCT ID: NCT03558321 Completed - Clinical trials for Postmenopausal Bleeding

Relation Between Human Epididymis Protein 4 (HE4) and Endometrial Pathology in Patients With Postmenopausal Bleeding

Start date: June 2014
Phase: N/A
Study type: Interventional

All patients included in the study had single or multiple episodes of postmenopausal bleeding with an endometrial thickness of more than 5mm. full history, general and local examination were done. Transvaginal ultrasound (TVS) was performed .The uterus was scanned in the sagittal plane. The double-layer ET was measured at the widest point between the endometrial-myometrial interfaces.the level of HE4 was measured. All women underwent hystrospopic guided endometrial biopsy. Definitive management was later performed in the form of total abdominal hysterectomy, bilateral salpingo oophrectomy, with or without pelvic lymph nodal dissection and histopathological examination.

NCT ID: NCT03558113 Not yet recruiting - Secondary Caries Clinical Trials

Reliability of Secondary Caries Detection Around Composite Restoration Using Light Induced Fluorescence

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

A total of 29 volunteer patients will be assigned in this study. Each patient should have one resin composite restoration. The restoration will be evaluated by two diagnostic methods (D), where D1 represents visual-tactile assessment method (modified USPHS) and D2 represents light induced fluorescence intraoral camera

NCT ID: NCT03557996 Not yet recruiting - Clinical trials for Dental Caries in Children

Discoloration of Carious Primary Teeth After Application of Silver Diamine Flouride Versus Sodium Fluoride Varnish

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

To assess discoloration of carious primary teeth after application of silver diamine fluoride versus sodium fluoride varnish.

NCT ID: NCT03557905 Recruiting - Clinical trials for Intraoperative Complications

Ultrasonographic Assessment of Lung Recruitment Maneuvers in Children Undergoing Lengthy Microsurgery Operations

RM
Start date: June 6, 2018
Phase: Phase 2
Study type: Interventional

The aim of this study will be to explore the clinical value of ultrasonic monitoring in the diagnosis of anesthesia-induced atelectasis, the assessment of the effects of lung recruitment, the best positive end-expiratory pressure (PEEP) after RM and in the detection of the point of lung re-collapse after RM in pediatric patients undergoing lengthy microsurgery operations.

NCT ID: NCT03557255 Completed - Heart Failure Clinical Trials

Levosimendan for Cardiac Patients Undergoing Major Abdominal Cancer Surgeries

Start date: August 1, 2017
Phase: Phase 2
Study type: Interventional

The objective of this pilot study is to evaluate the efficacy and safety of preoperative administration of levosimendan in patients with chronic heart failure scheduled for major abdominal cancer surgery assuming the reduction of both perioperative morbidity and mortality.

NCT ID: NCT03556852 Completed - Clinical trials for Postpartum Hemorrhage

CARBETOCIN VERSUS RECTAL MISOPROSTOL FOR MANAGEMENT OF THIRD STAGE OF LABOR IN WOMEN AT LOW RISK OF POSTPARTUM HEMORRHAGE

Start date: July 2, 2017
Phase: Phase 4
Study type: Interventional

150 pregnant women admitted for spontaneous, induced or augmented vaginal delivery and categorized as low risk for postpartum hemorrhage (PPH) were divided randomly into two groups. Carbetocin group (C) received 1 ampoule of Carbetocin (100 μg/ml) (Pabal®, Draxis/Multipharma, Egypt, under license from DRAXIS PHARMA-Canada) added to 10 cc saline and given IV after the delivery of the baby. Misoprostol group (M) received 2 rectal misoprostol tablets (800 μg) (Misotac; SIGMA Pharm, Cairo, Egypt) after the delivery of the baby. Blood samples were tested to measure hemoglobin levels upon admission to the labor room and 12 hours after delivery

NCT ID: NCT03556111 Not yet recruiting - Alveolar Bone Loss Clinical Trials

Evaluation of Efficiency of Autogenous Particulate Sticky Bone Preparation (With and Without Xenograft Usage) for Grafting of Maxillary Anterior Knife Edge Ridge in Partially Edentulous Patients for Esthetic Implant Placement

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

The aim is to evaluate the value and efficiency of sticky bone in the augmentation of alveolar ridge deficiency when being used with or without xenogenic bone graft for esthetic implant placement.

NCT ID: NCT03554980 Not yet recruiting - Clinical trials for Dental Caries in Children

Application of SDF Verses NaF Varnish in Treatment of Carious Primary Teeth

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

The aim of this study is to assess the postoperative pain after application of silver diamine fluoride versus sodium fluoride varnish in treatment of carious primary teeth.

NCT ID: NCT03552640 Not yet recruiting - Clinical trials for Orthodontic Appliance Complication

Accuracy of Digital Three-Dimensional Root Position Prediction Via Digitized Models

Start date: June 2018
Phase:
Study type: Observational

Measuring the accuracy of a new technique by which root positions can be predicted at the pre-finishing stage of the comprehensive orthoodntic treatment

NCT ID: NCT03552510 Recruiting - Preterm Infant Clinical Trials

Oropharyngeal Administration of Mother's Milk in Preterm Infants and Gastrointestinal Motility

OPAMM
Start date: June 1, 2016
Phase: N/A
Study type: Interventional

Mother's milk does not come in contact with the oropharyngeal pouch of preterm infants during gavage feeding. We hypothesized that stimulation of the oropharyngeal pouch using small amount of the mother's milk 5 minutes before initiation of regular gavage feeding will increase the level of GIT hormones.