Clinical trials: sponsored by Benha University
Complications; Cesarean Section
Methods of Placental Delivery and the Amount of Blood Loss During Cesarean Section
To compare between the effect of controlled cord traction and manual removal of the placenta on blood loss among women undergoing caesarean sections
- Trial name
- NCT02405663
- Testing
- manual removal, cord traction
- Where
- Saudi Arabia
- Volunteers
- 288 people
- Sponsor
- Benha University
Depression, Hemodialysis Complication
Intravenous Iron May Increase Depression Among Hemodialysis Patients
the aim of this study is to assess whether increased ferritin after intravenous iron therapy will lead to increased prevalence of major depression among treated patients.
- Conditions
- Depression, Hemodialysis Complication, Iron Deficiency Anemia
- Trial name
- NCT03157050
- Testing
- Intravenous iron therapy
- Volunteers
- 112 people
- Sponsor
- Benha University
Hyperuricemia, Hemodialysis Complication
Use of Febuxostat in Hyperuricemia Among Hemodialysis Patients
Hyperuricemia is not infrequently encountered among hemodialysis patients. However, there is no clear data about use of febuxostat among hemodialysis patients, apart from very small case series.
- Trial name
- NCT03149939
- Testing
- Febuxostat 40 milligramsTablet
- Volunteers
- 19 people
- Sponsor
- Benha University
Secondary Hyperparathyroidism, Diabetic Nephropathies
Prevalence of Secondary Hyperparathyroidism Among Patients With Diabetic Nephropathy
The aim of this study is to evaluate the prevalence of secondary hyperparathyroidism among patients with diabetic nephropathy.
- Trial name
- NCT03137316
- Testing
- intact parathyroid hormone level
- Volunteers
- 437 people
- Sponsor
- Benha University
Acute Kidney Injury
Serum Procalcitonin Level May Predict Acute Kidney Injury in ICU Patients With Sepsis
The aim of this study is to examine if procalcitonin (PCT) can be used for early prediction of AKI septic patients in ICU.
- Trial name
- NCT03097393
- Testing
- measure Serum procalcitonin level
- Volunteers
- 67 people
- Sponsor
- Benha University
Infertility
Outcome of Cetrotide Therapy for Management of Women at High-risk of Ovarian Hyperstimulation Syndrome
To evaluate safety and efficacy of 3-day cetrotide therapy started on day of oocyte retrieval (Day-0) in women at high-risk for development of ovarian hyperstimulation syndrome (OHSS) after gonadotropin- releasing hormon agonist…
- Trial name
- NCT02823080
- Testing
- Cetrorelix
- Where
- Egypt
- Volunteers
- 48 people
- Sponsor
- Benha University
Postmenopausal Bleeding
Uterine Artery and Spiral Artery Doppler Parameters in Patients With Postmenopausal Bleeding
This study was to investigate the diagnostic value of ultrasonography and blood flow measurements in uterine arteries and spiral arteries by transvaginal color Doppler ultrasonography in the detection of the endometrial pathology…
- Trial name
- NCT02822885
- Testing
- Ultrasonography
- Where
- Egypt
- Volunteers
- 70 people
- Sponsor
- Benha University
Infertility
Endometrial Injury for Unexplained Infertility
One hundred and twenty women with unexplained infertility were included in the study. Divided randomly into two groups: Group I: (60 patients): (control group) Group II (60 patients): (study group) All the patients received (CC)…
- Trial name
- NCT02863198
- Testing
- endometrial injury
- Where
- Egypt
- Volunteers
- 120 people
- Sponsor
- Benha University
Infertility
Calcium Dobesilate Versus Cabergoline for Prevention of Ovarian Hyperstimulation Syndrome
The purpose of this study is to compare the effect of oral Calcium Dobesilate to oral Cabergoline in the prevention of ovarian hyperstimulation syndrome (OHSS) in high-risk women underwent intracytoplasmic sperm injection (ICSI).
- Trial name
- NCT02271360
- Testing
- Calcium Dobesilate, Cabergoline
- Where
- Egypt
- Volunteers
- 200 people
- Sponsor
- Benha University
Hemodialysis-Induced Symptom
Use Of Blood Flow Rate Profiling For Postdialysis Washed-Out Patients
Hemodialysis patients frequently complain of postdialysis fatigue and washed-out feeling. The aim of this study is to use blood flow rate (BFR) profiling to mitigate postdialysis washed-out state.
- Trial name
- NCT03037138
- Testing
- Blood flow Rate profiling
- Volunteers
- 27 people
- Sponsor
- Benha University
Oligoasthenoteratozoospermia
Severe Male Factor Infertility Management
This study is the first to evaluate the effect of oral supplementation with antioxidants combined with lifestyle modification for severe male factor partner of couples undergoing ICSI.
- Trial name
- OAT (NCT02752555)
- Testing
- Antioxidant (l-cratinine) + modifiable lifestyle factors
- Where
- 3 sites in Egypt
- Volunteers
- 60 people
- Sponsor
- Benha University
Infertility
Predictive Value of Endometrial Cytokines in Endometrial Implantation in Cases of Intracytoplasmic Sperm Injection
For all women immediately after ovum retrieval from 80 women undergoing IVF, intra uterine salin flushing will be analyzed using a multiplex immunoassay for soluble regulators of implantation, namely Interleukin (IL)-1b, Tumor…
- Trial name
- NCT02854514
- Testing
- Aspiration of endometrial secretion
- Where
- Egypt
- Volunteers
- 80 people
- Sponsor
- Benha University
Infertility
Multi-factorial Analysis of the Follicular Fluid Milieu to Explore the Discrepant Effect of Follicular Fluid Endometrial Flushing on Outcome of Assisted Reproduction Trial
Patients \& Methods: Eighty infertile women were randomly categorized into: Group EF (n=40) had EF after oocyte retrieval and Control group (n=40) did not have EF.
- Trial name
- NCT02468258
- Testing
- endometrial flushing
- Where
- Egypt
- Sponsor
- Benha University
Infertility
Extended Clomiphene Citrate Regimen in Women With Polycystic Ovary Syndrome
One hundred and thirty six anovulatory women with CC-resistant PCOS were scheduled randomly into two equal groups. Group A (n=68); received CC (100 mg/day from cycle day 3 for 10 days) for up to six cycles.
- Trial name
- NCT02381184
- Testing
- clomiphene citrate, laparoscopic ovarian drilling (LOD)
- Where
- Egypt
- Volunteers
- 160 people
- Sponsor
- Benha University
Unexplained Infertility
Dual FSH/HCG Trigger in Letrozole Stimulated Intrauterine Insemination Cycles in Women With Unexplained Infertility
The objective of this study was to evaluate the outcome of follicle stimulating hormone (FSH) co-administration with human chorionic gonadotrophins trigger for women with unexplained infertility (UEI) and assigned for letrozole…
- Trial name
- NCT02739516
- Testing
- Human chorionic gonadotropin, FSH co-trigger, Letrozole
- Volunteers
- 108 people
- Sponsor
- Benha University
Isolated (Idiopathic) Oligohydramnios
Nitric Oxide Donors for Treatment of Isolated Oligohydramnios
Objective: To assess the influence of maternal isosorbide mononitrate (IMN) vaginal supplementation in improving liquor volume in women with isolated oligohydramnios. Study Design: Prospective randomized interventional study.
- Trial name
- NCT02712125
- Testing
- isosorbide mononitrate
- Volunteers
- 100 people
- Sponsor
- Benha University
Postcesarean Pain Relief
Efficacy of Intraperitoneal Versus Intravenous Lidocaine for Postcesarean Pain Relief
Objective: To evaluate intraperitoneal (IP) lidocaine administration and intravenous (IV) lidocaine infusion for postoperative pain control after cesarean section.
- Trial name
- NCT02707081
- Testing
- Intravenous normal saline, Intraperitoneal normal saline, Intraperitoneal Lidocaine
- Volunteers
- 150 people
- Sponsor
- Benha University
Infertility
Diosmin Versus Cabergoline for Prevention of Ovarian Hyperstimulation Syndrome
The purpose of this study is to compare the effect of oral Diosmin to oral Cabergoline in the prevention of ovarian hyperstimulation syndrome (OHSS) in high-risk women underwent intracytoplasmic sperm injection (ICSI).
- Trial name
- infertility (NCT02134249)
- Testing
- Diosmin, Cabergoline
- Where
- 2 sites in Egypt
- Volunteers
- 200 people
- Sponsor
- Benha University
Ultrasound Quality
Can Increased Body Mass Index Prevent Adequate Ultrasound Examination for Trisomy 21 Risk Assessment?
Determine Cutoff BMI at which transabdominal sonography (TAS) is not satisfactory for aneuploidy risk assessment.
- Trial name
- NCT02443597
- Testing
- ultrasound
- Where
- Saudi Arabia
- Volunteers
- 200 people
- Sponsor
- Benha University
Placenta Previa Complete Centralis
the Treatment of Postpartum Hemorrhage Due to Placenta Previa Complete Centralis
Objective: To assess the efficacy of lower uterine compression sutures (involved bilateral uterine artery ligation and compression of the lower uterine segment at the same time with one circular stitch) as a conservative…
- Trial name
- PPH (NCT02157441)
- Testing
- lower uterine compression sutures
- Where
- Egypt
- Volunteers
- 50 people
- Sponsor
- Benha University