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NCT ID: NCT03402165 Recruiting - Hepatitis C Clinical Trials

Serum Alpha-fetoprotein Levels and Response to Direct Antiviral Therapy in Patients With Chronic Hepatitis C

Start date: January 1, 2017
Phase: Phase 4
Study type: Interventional

Alpha-fetoprotein Levels on the Response to direct Antiviral Therapy in Patients with Chronic Hepatitis C

NCT ID: NCT03398863 Recruiting - Pregnancy Clinical Trials

Intra-uterine Cleaning During Cesarean Section

Start date: February 5, 2018
Phase: N/A
Study type: Interventional

400 women who came to our Department for Cesarean Section delivery will be divided into 2 groups: Group1:Cleaning the uterine cavity "200 patients" Group2:No Cleaning of uterine cavity "200 patients"

NCT ID: NCT03398031 Recruiting - ICSI Clinical Trials

Effect of Magnesium Supplement in Early Pregnancy After ICSI

Start date: June 1, 2017
Phase: Phase 3
Study type: Interventional

Daily supplement of magnesium after biochemical diagnosis of pregnancy in females pregnant after ICSI and through out 1st trimester

NCT ID: NCT03397615 Recruiting - Puerperal Infection Clinical Trials

Effect of Vaginal Douching With Betadine Before CS for Prevention of Post Operative Infections

Start date: January 3, 2019
Phase: N/A
Study type: Interventional

The present study was a prospective randomized controlled trial in which subjects received a vaginal preparation with povidone-iodine solution immediately prior to caesarean delivery or received no vaginal preparation

NCT ID: NCT03397381 Recruiting - Clinical trials for Chronic Renal Failure

Outcome of Arterio-venous Fistula for Adult Hemodialysis Patients in Assiut Governorate

Start date: January 20, 2018
Phase:
Study type: Observational

identification of the factors that affect the outcome of arteriovenous fistula in chronic renal failure patients that newly established regular dialysis in Assiut Governorate 1. To study the factors that influence the outcome of AVF 2. To evaluate the vascular complications of AVF as occlusion, rupture, aneurysmal dilation and hand ischemia

NCT ID: NCT03397368 Recruiting - Clinical trials for Stress Incontinence, Female

Evaluation of Transperineal US in Stress Incontinence

Start date: January 16, 2018
Phase:
Study type: Observational [Patient Registry]

Stress urinary incontinence (SUI) has an observed prevalence of between 4%and 35%.Identified risk factors are aging, obesity and repeated pregnancies and deliveries. Urodynamic remains the gold standard for diagnosis in the past years. Trans labial ultrasound appears to have a good role in diagnosing stress incontinence

NCT ID: NCT03397316 Recruiting - Bone Loss Clinical Trials

Evaluation of Marginal Bone Loss After Immediate Implant Placement in Esthetic Zone Without Xenograft.

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

Marginal bone loss in immediate implant placement in upper esthetic zone by comparing between non grafting in immediate implant placement with xenograft placement in other side. the study is to assess the marginal bone loss in the two techniques and compare results between them.

NCT ID: NCT03396380 Recruiting - Ovulation Induction Clinical Trials

Effect of Vitamin D Supplement in Induction of Ovulation in Overweight Women With Polycystic Ovary Syndrome

Start date: July 1, 2017
Phase: Phase 3
Study type: Interventional

The aim of this work is to evaluate the effect of vitamin D supplementation in overweight infertile women with PCOs undergoing induction of ovulation.

NCT ID: NCT03395730 Recruiting - Clinical trials for Postpartum Haemorrhage With Retained Placenta

Intraumbilical Oxytocin Versus Placental Cord Drainage in the Management of 3rd Stage of Labor

Start date: September 30, 2017
Phase: Phase 2
Study type: Interventional

The aim of this study is to compare the effectiveness of intraumbilical oxytocin and placental cord drainage in the management of third stage of labor. Does the use of intraumbilical vein oxytocin injection or the use of Placental cord drainage can cause a reduction of blood loss, Hb level drop, the length of the third stage of labor and the incidence of manual removal of the retained placenta during the third stage of labor in pregnant women after delivery of the infant?

NCT ID: NCT03394625 Recruiting - Clinical trials for Marginal Bone Loss in Socket Shield Technique

Evaluate Marginal B. Loss in Immediate Implant Placement in Maxillary Esthetic Zone Using Socket Shield Versus Xenograft

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

Anterior maxilla (Esthetic zone) is very challenging area because of thin buccal plate of bone. After tooth extraction physiological process occur causing alteration of bone and soft tissue so, delayed placement of implant lead to loss of bone height and width. Immediate placement of implant is become essential to preserve the bone and soft tissue from loss. Socket shield technique is a recent technique which is by sectioning the root and extraction of palatal part and leaving buccal part of the root with its attachment of periodontal ligament and vascularization still intact then placing implant in palatal socket. This technique allow preservation of buccal plate of bone and soft tissue with minimum loss allowing better result in esthetic zone.