Clinical Trials Logo

Filter by:
NCT ID: NCT01649752 Recruiting - Clinical trials for Assess the Efficacy of Differentiated and Undifferentiated Stem Cell Therapy in Improving Endometrial Receptivity.

Role of Stem Cells in Improving Implantation Rates in ICSI Patients

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

Background: Improving implantation rates in ICSI cycles has been the focus of research in recent decades. Because success rates is not satisfactory enough especially when transferring good embryos to the uterine cavity and pregnancy does not occur. Trying to improve endometrial receptivity, the investigators have thought about stem cell therapy as stem cells have played a pivotal role in regenerative medicine in many pathologies as myocardial infarction, Diabetes Mellitus and spinal cord injuries. Garget and Healy reported in 2011 treatment of a case with Asherman's syndrome by administration of bone marrow stem cells in the uterine cavity. Endometrial growth and improved vascularity has been observed by ultrasound follow-up and Doppler study of endometrial blood flow. Endometrial regeneration has been enough to support pregnancy through successful IVF trial. The investigators have succeeded in previous work to isolate MSC from placental tissue and differentiate it to endometrium-like cells. The investigators compared the differentiation ability of placental derived mesenchymal stem cells (MSC) and Wharton Jelly derived MSC to differentiate to endometrium under 3 different culture conditions: endometrium conditioned medium (ECM), follicular fluid (FF) conditioned medium and medium containing both. The investigators found that placental MSC has better differentiating ability to endometrium especially under culture conditions containing both ECM and FF as evidenced by prominent appearance of glandular pattern and expression of progesterone receptors in differentiated cells. Therefore the investigators need to direct this study and test the effect of placental derived MSC in improving implantation rates in patients with recurrent implantation failure, unresponsive endometrium to ovulation induction drugs or with endometrial atrophy or advanced maternal age planning for ICSI trial. Patients and Methods: 60 patients attending Kasr El-Aini assisted reproduction unit and private IVF center will be randomized to three groups by computer generated programs: The first group, patients randomized to receive differentiated stem cell therapy: After ovum pick-up, MSC differentiated to endometrium is deposited in the uterine cavity through an IUI catheter. Embryo transfer will be done at day 5 at the blastocyst stage to allow enough time for endometrial regeneration and increased endometrial receptivity. The second group, patients randomized to receive undifferentiated stem cell therapy: Immediately postmenstrual undifferentiated MSC is deposited in the uterine cavity through an IUI catheter to allow enough time for the MSC to differentiate as it needs 7-10 days for differentiation. Ovum pick-up will be done as usual while all other steps will be the same including embryo transfer which will be done at day 5. The third group, control group: Patients are randomized to receive no stem cell therapy; All ICSI steps from ovulation induction protocol to embryo transfer conditions will be the same for all groups. Informed consent will be taken from the patients after detailed explanation of all steps of the procedure.

NCT ID: NCT01649245 Recruiting - Chronic Hepatitis C Clinical Trials

Hansenula-derived Pegylated Interferon in Treatment of Patients With Chronic Hepatitis C

HAPIC
Start date: August 2012
Phase: Phase 4
Study type: Interventional

It is a multi-center study of the efficacy of a new Pegylated Hansenula-derived recombinant interferon α 2a (Reiferon Retard® 160 µg once weekly in combination with ribavirin in treatment of Egyptian patients with chronic hepatitis C for 48 weeks. hepatitis C virus (HCV) viral load will be assessed during therapy at weeks 12, 24 and end of treatment, as well as 24 weeks after therapy is completed.

NCT ID: NCT01646619 Recruiting - Clinical trials for Severe Hypoxic Ischemic Encephalopathy

Efficacy Study of Hypothermia Plus Magnesium Sulphate(MgSO4) in the Management of Term and Near Term Babies With Hypoxic Ischemic Encephalopathy

MagCool
Start date: May 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess whether the addition of a drug such as Magnesium sulphate while providing therapeutic hypothermia (or cooling) to babies who are asphyxiated at birth provides additional benefit to the babies' survival and outcome compared to cooling alone.

NCT ID: NCT01635426 Recruiting - Clinical trials for Recurrent Pregnancy Loss

Aspirin Versus Clopidogrel Effect on Uterine Blood Flow in Women With Unexplained Recurrent Miscarriages

Start date: March 2012
Phase: Phase 2/Phase 3
Study type: Interventional

The study will compare the effect of Aspirin versus clopidogrel effect on uterine perfusion in women with unexplained recurrent pregnancy loss with decreased uterine artery pulsatility index. Null hypothesis: Women with recurrent miscarriage have the same blood flow after aspirin or clopidogrel treatment compared to their uterine artery pulsatility index before treatment.

NCT ID: NCT01634633 Recruiting - Clinical trials for Gynecological Pathologies

Endometrial Nerve Fibers Detection in Patients With Different Gynecological Pathologies

Start date: January 2011
Phase: N/A
Study type: Observational

The aim of this study is to investigate the prevelence of endometrial nerve fibers in different gynecological pathologies

NCT ID: NCT01600612 Recruiting - Clinical trials for Postpartum Hemorrhage

Oxytocin, Carbetocin and Misopristol for Treatment of Postpartum Hemorrhage: A Multicentric Randomized Trial

Start date: September 2012
Phase: N/A
Study type: Interventional

Postpartum hemorrhage (PPH) is the leading cause of maternal death worldwide, with an estimated mortality of 140 000 per year. Uterine atony is one of the most important causes of PPH. The traditional treatment of which is the use of uterotonic agents. Oxytocin is the most conventional drug which was proved effective. However, it has the shortcomings of short half life and the necessity of intravenous administration. Misopristol, and more recently Carbetocin were introduced for treatment of atonic PPP not responding to Oxytocin. Aim of the study is to evaluate the effectiveness of Carbetocin, Misopristol, and Oxytocin for treatment of atonic PPH.

NCT ID: NCT01529177 Recruiting - Infertility Clinical Trials

Metformin for the Treatment of Unexplained Oligozspermia

Start date: February 2012
Phase: Phase 4
Study type: Interventional

Insulin resistance (IR) in men may be the underlying pathogenesis for metabolic abnormalities and chronic hypospermatogenesis similar to women with polycystic ovarian disease (PCOD). Infertile men with unexplained infertility and IR may benefit from treatment with metformin.

NCT ID: NCT01523327 Recruiting - Clinical trials for Uric Acid and Hypertension in Pregnancy

Study of Association Between Maternal Uric Acid , Maternal and Fetal Outcome in Pregnant Women With Hypertension

Start date: October 2011
Phase: N/A
Study type: Observational

Association of maternal uric acid with maternal condition and fetal outcome in pregnant women with hypertension.

NCT ID: NCT01520090 Recruiting - Contraception Clinical Trials

Egyptian Women Knowledge and Use of Different Contraceptive Methods

Start date: January 2012
Phase: N/A
Study type: Observational

Starting from Jan 2012 for an interval of 4 months with minimum number of 1200 egyptian women will be asked to complete a questionairre to evaluate their knowledge of different contraceptive methods

NCT ID: NCT01518816 Recruiting - Preterm Labor Clinical Trials

Role of Serum Total Antioxidant Level in Preterm Labor

Start date: October 2011
Phase: N/A
Study type: Observational

The aim of this study is to detect the association between maternal serum antioxidant level and preterm labor.