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NCT ID: NCT02410759 Recruiting - Clinical trials for Post Partum Hemorrhage

Carbetocin Versus Ergometrine in the Management of Atonic Post Partum Haemorrhage (PPH) in Women Delivered Vaginally

Start date: April 2015
Phase: Phase 3
Study type: Interventional

200 women will be randomly divided into 2 equal groups using computer generated random numbers. Group 1 will receive Carbetocin 100 µgm (Pabal® Ferring, UK) and group 2 will receive ergometrine 0.5mg (methergin®, Novartis, Switzerland).

NCT ID: NCT02409407 Recruiting - Infertility Clinical Trials

Misoprostol Before Hysteroscopy in Infertile Cases

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

The role of hysteroscopy in infertility investigation is to detect possible intrauterine changes that could interfere with implantation or growth or both of the conceptus, with the invention of miniature hysteroscope, it is possible to perform hysteroscopy in an office setting (Outpatient hysteroscopy; OH), for diagnostic and certain therapeutic intervention. It is currently acknowledged as the 'gold standard' investigation of the intrauterine abnormalities. Cervical priming prior to diagnostic hysteroscopy softens the cervix and lessens the force needed for dilation, thereby potentially reducing the probability of procedural complication such as uterine perforation, cervical laceration, failure to dilate, and creation of a false track that can occur during cervical entry. Misoprostol is a prostaglandin El analogue, that can be administered either orally or vaginally, that can cause cervical ripening by inducing collagenolytic activity and synthesis of proteoglycans.

NCT ID: NCT02405637 Recruiting - Clinical trials for Necrotizing Enterocolitis

Simulated Amniotic Fluid In Preventing Feeding Intolerance and Necrotizing Enterocolitis VLBW Neonates

Start date: March 2014
Phase: Phase 1
Study type: Interventional

The human fetus swallows over 200 ml of amniotic fluid per kilogram of weight each day and such swallowing is essential for normal small bowel development.Growth factors found in the amniotic fluid have been shown to promote proliferation of fetal intestinal cells. As feeding intolerance is a common problem among premature neonates, the investigators will study the role of enteral administration of simulated amniotic fluid solution in prevention of feeding intolerance and NEC in premature neonates.

NCT ID: NCT02401438 Recruiting - Prematurity Clinical Trials

Accuracy of 5D LB Ultrasound in Predicting Birth Weight of Preterm Fetuses : A Pilot Study

Start date: March 2015
Phase:
Study type: Observational

5D and 2D ultrasound will be done for pregnant women within 72hours before preterm delivery to determine estimated fetal weight by ultrasound. The estimated fetal weight by 5D and 2D ultrasound will be compared to the actual birth weight to determine accuracy of 5D ultrasound in predicting actual birth weight .

NCT ID: NCT02396329 Recruiting - Clinical trials for Surgical Site Infection

Chlorhexidine Versus Povidone-Iodine Antisepsis for Reduction of Post Cesarean Section Surgical Site Infection

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

There is no difference between using chlorhexidine-based antisepsis protocol versus povidone-iodine protocol in reduction of surgical site infection in women undergoing cesarean section.

NCT ID: NCT02387333 Recruiting - Parastomal Hernia Clinical Trials

Role of Mesh Stoma Reinforcement Technique (MSRT) in Prevention of Parastomal Hernia After Ileal Conduit Urinary Diversion

Start date: February 2015
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of this clinical trial is to investigate the safety and efficacy of prophylactic mesh on prevention of parastomal hernia(PSH) after ileal conduit urinary diversion (IC) in a randomized controlled fashion.

NCT ID: NCT02383394 Recruiting - Clinical trials for Invitro Fertilization

Factors Associated With Pregnancy Loss in IVF Women

Start date: April 2015
Phase: N/A
Study type: Observational

Maternal and clinical characteristics associated with spontaneous second-trimester pregnancy loss (between 12 1/7 and 23 6/7 weeks of gestation) will be assessed.

NCT ID: NCT02380560 Recruiting - Clinical trials for Fetal Membranes, Premature Rupture

Myometrial Thickness as a Predictor for the Latency Interval in PPROM

Start date: March 1, 2018
Phase: N/A
Study type: Observational

100 women divided into 3 groups: - Group I: included 50 women with preterm premature rupture of membranes (PPROM, n=50) with gestational age from 24 to 34 weeks. - Group II: included 25 term non-labor control (T-CTR, n=25) with gestational age from 37 to 41 weeks. - Group III: included 25 preterm non-labor control (P-CTR, n=25) with gestational age from 24 to 34 weeks.The myometrial thickness at 4 different sites9: a) The lower uterine segment (LUS): 2cm above the reflection of the full urinary bladder (b)The anterior wall: 1cm above the maternal umbilicus. (c)Fundus: by placing the scan probe perpendicularly above the uterine fundus so that the entire curvature of the uterus was visualized. (d)The posterior wall: through using the maternal abdominal aortic pulsation as an anatomic marker. At least 3 measurements were obtained at each site and averaged. The latency interval is determined in each of the 3 groups.

NCT ID: NCT02372487 Recruiting - Clinical trials for Pregnancy Complication

Sildenafil Citrate Therapy for Oligohydramnios

Start date: March 2015
Phase: N/A
Study type: Interventional

The aim of this randomized trial is to detect whether or not the use of Sildenafil citrate therapy will increase the amniotic fluid volume expressed in term of amniotic fluid index measured via ultrasound for fetuses of pregnancies complicated by oligohydramnios, and to compare the outcomes of Sildenafil-treated pregnancies with similar pregnancies that will remain Sildenafil-naïve.

NCT ID: NCT02356744 Recruiting - Clinical trials for Pregnancy, Complications

Maternal and Neonatal Outcome in Pregnant Women Before and After 1 Year Since Bariatric Operation

Start date: February 2, 2016
Phase: N/A
Study type: Observational

Ultrasound follow up for 9 months pregnancy in women underwent baraitric surgery before and after 1 year of surgery.