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NCT ID: NCT02351336 Recruiting - Preterm Labour Clinical Trials

Fetal Adrenal Gland Volume Estimation Compared to Cervical Length Assessment in Prediction of Preterm Birth

Start date: August 2014
Phase: N/A
Study type: Observational

If the investigators could prove that three -dimensional ultrasound measurement of fetal adrenal gland volume can accurately predict the likelihood of preterm birth in patients having symptoms and signs of PTL , they would be able to use it as a valuable component for assessment and early management of high risk pregnant women for PTB which can be positively reflected on the risk of neonatal morbidity and mortality in those patients.

NCT ID: NCT02350179 Recruiting - Clinical trials for Hemorrhage of Cesarean Section and/or Perineal Wound

Efficacy of Tranexamic Acid in Reducing Blood Loss During and After Caesarean Section

Start date: June 2014
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is to evaluate the efficacy of tranexamic acid in reducing blood loss during and after elective C.S. The Research Question Is Tranexamic acid effective in reducing blood loss during and after elective Caesarean section? The Research Hypothesis The TXA could be able to reduce blood loss during and after elective Caesarean section. The null hypothesis will therefore state that: There will be no difference between TXA and placebo in reducing blood loss during and after elective Caesarean section.

NCT ID: NCT02345837 Recruiting - Clinical trials for Asymptomatic Diseases

Effect of Local Endometrial Injury on Pregnancy Outcomes During Ovulation Induction Cycles

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

The aim of this study is to detect whether or not performing an endometrial sampling in the cycle preceding ovulation induction with clomiphene citrate can improve pregnancy outcomes in the next cycle.

NCT ID: NCT02344888 Recruiting - Infertility Clinical Trials

Adding Prednisolone During Ovulation Induction With CC in Lean Women With CC Resistant PCOS

Start date: February 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effect of concomitant administration of prednisolone during use of clomiphene citrate (CC) for induction of ovulation in infertile lean women having CC resistant polycystic ovarian syndrome (PCOS).

NCT ID: NCT02343562 Recruiting - Clinical trials for Hirschsprung Disease

Probiotics for Prophylaxis of Postoperative Hirschsprungs Associated Enterocolitis

Start date: October 2014
Phase: Phase 4
Study type: Interventional

Hirschsprungs Associated Enterocolitis (HAEC) with incidence up to 30% postoperatively. The objective of the trial is to prevent postoperative HAEC by using Probiotics.

NCT ID: NCT02339623 Recruiting - Preterm Birth Clinical Trials

Fetal Adrenal Gland Volume Estimation in Prediction of Preterm Birth

Start date: August 2014
Phase: N/A
Study type: Observational

If we could prove that three -dimensional ultrasound measurement of fetal adrenal gland volume can accurately predict the likelihood of preterm birth in patients having symptoms and signs of PTL , we would be able to use it as a valuable component for assessment and early management of high risk pregnant women for PTB which can be positively reflected on the risk of neonatal morbidity and mortality in those patients.

NCT ID: NCT02337881 Recruiting - Clinical trials for Labor Preterm Requiring Hospitalization

Management of Acute Preterm Labor: Nifedipen Alone or Combined With Cildenafil Citrate

Start date: January 2015
Phase: Phase 1
Study type: Interventional

The aim of this study is to assess whether or not the emergency tocolytic effect of combined nifedipine and sildenafil citrate will have a superior effect over nifedipine alone in terms of inhibiting eminent preterm labor and improving perinatal outcomes.

NCT ID: NCT02335736 Recruiting - Infertility Clinical Trials

Antagonist Protocol in IVF

Start date: January 2015
Phase: Phase 2
Study type: Interventional

The antagonist protocol in a novel method of stimulation in the in vitro fertilization (IVF) patients. It has been tried in poor responders, polycystic ovary (PCO) patients and normal females undergoing IVF. Can it be used with the same efficacy in all patients?

NCT ID: NCT02334163 Recruiting - Clinical trials for Hepatic Encephalopathy

The Effects of Nitazoxanide in Hepatic Encephalopathy

Start date: December 2014
Phase: Phase 2
Study type: Interventional

Evaluating the efficacy and safety of nitazoxanide in comparison to standard treatment in patients with grade II-III hepatic encephalopathy (HE). Also, Evaluating the effect of administering nitazoxanide on the improvement of patient's quality of life.

NCT ID: NCT02331199 Recruiting - Preterm Labour Clinical Trials

Comparison Between Amniotic Fluid Lamellar Body Count and Fetal Pulmonary Artery Doppler Indices in Predicting Fetal Lung Maturity

Start date: December 2014
Phase: Phase 3
Study type: Interventional

The investigators will study 200 women with singleton pregnancies presented with prelabor preterm rupture of membranes or undergoing cesarean section (CS). Amniotic fluid lamellar body count (LBC) and fetal pulmonary artery Doppler will be done to all women. LBC and fetal pulmonary artery Doppler will be correlated with fetal outcome