Clinical trials: Fetus Fetus
Induction of Labor Affected Fetus / Newborn
Vaginal Misoprostol and Foley Catheter for Induction of Labor
to compare between sequential and concurrent use of vaginal misopristol plus foleys catheter for induction of labor
- Trial name
- NCT02952807
- Testing
- Misoprostol, Foley Catheter
- Where
- Egypt
- Volunteers
- 160 people, healthy volunteers welcome
- Sponsor
- Zagazig University
Umbilical Cord; Complications, Affecting Fetus
Perinatal Outcomes in Umbilical Cord Entanglement
Umbilical Cord Entanglement and Perinatal Outcomes.
- Trial name
- AssiutU (NCT03504969)
- Volunteers
- 201 people, healthy volunteers welcome
- Sponsor
- Assiut University
Induction of Labor Affected Fetus / Newborn
A Comparison Between the Effect of Oxytocin Only and Oxytocin Plus Propranolol on Induction of Labor in Term Pregnancy
The present study is conducted to compare the effect of Oral Propranolol and Oxytocin, versus Oxytocin only on induction of labor in term pregnancy.
- Trial name
- NCT03533699
- Testing
- Propranolol
- Where
- Egypt
- Volunteers
- 202 people, healthy volunteers welcome
- Sponsor
- Ain Shams Maternity Hospital
Induction of Labor Affected Fetus / Newborn
The Impact of a Customized Informative Video Prior to Induction of Labor on Anxiety Relieve.
To determine whether watching a personalized video prior to medically indicated labor induction among term parturients reduces anxiety levels according to the STAI questionnaire, compared to a standard counselling.
- Trial name
- NCT06375746
- Testing
- Personalized video
- Where
- Israel
- Volunteers
- 180 people, healthy volunteers welcome
- Sponsor
- Wolfson Medical Center
Induction of Labor Affected Fetus / Newborn
Vaginal Misoprostol With Intracervical Foley Catheter in Induction of Labor
The aim of present study is to compare the safety and efficacy of vaginal misoprostol versus the combination of vaginal misoprostol and intracervical Foley catheter in induction of labor at term pregnancy.
- Trial name
- NCT03682718
- Testing
- Transcervical Foley catheter, Misoprostol
- Where
- Egypt
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Ain Shams University
Dystocia; Fetal, Labor Long
Mouth Guard Use in the Second Stage of Labor
Shortening the second stage of labor, the time spent pushing the baby out, is important for positive mother and infant's outcomes.
- Conditions
- Dystocia; Fetal, Labor Long, Cesarean Section, Affecting Fetus or Newborn
- Trial name
- NCT03520530
- Testing
- Mouth Guard
- Where
- United States
- Volunteers
- 154 people, healthy volunteers welcome
- Sponsor
- Christiana Care Health Services
Identification of the Mother or Fetus Contamination by SARS Cov-2, Research the Presence of Viruses at Different Sites of the Mother and the Fetus or Father
Study of Late Fetal Loss in Poitou-Charentes. GYNE-COVID
Maternal-fetal transmission in the second or third trimester of pregnancy of the SARS-COV-2 virus could explain some late fetal losses. Finding a cause in the context of fetal loss is essential for parents and caregivers.
- Conditions
- Identification of the Mother or Fetus Contamination by SARS Cov-2, Research the Presence of Viruses at Different Sites of the Mother and the Fetus or Father, The Survey Builds on a Network Work Already Organized Around the CPDPN of Poitou-Charentes, Analysis Laboratories of the Poitiers CHU
- Trial name
- NCT04387253
- Testing
- Identification by PCR of the SARS-COV-2 virus in samples taken from the fetus
- Where
- France
- Volunteers
- 28 people, healthy volunteers welcome
- Sponsor
- Poitiers University Hospital
Maternal Death Affecting Fetus or Newborn, Delivery Complication
Impact of a Smartphone Intervention on Tanzanian Women's Childbirth Location
This study investigates whether training Community Health Workers (CHW) to use a smartphone-based prenatal counseling application as a "job aid" instead of the existing paper based standard is associated with increased women's…
- Conditions
- Maternal Death Affecting Fetus or Newborn, Delivery Complication, Obstetric Complication, Birth Injuries
- Trial name
- SUSTAIN1 (NCT03161184)
- Testing
- SUSTAIN Smartphone training of CHW (SP+), SUSTAIN Paperbased training of CHW (SOC)
- Volunteers
- 572 people, healthy volunteers welcome
- Sponsor
- University of Toronto
Medical; Abortion, Fetus
Fertility and Obstetric Outcomes After Medical Management Versus Surgical Treatment for First-trimester Miscarriage First-trimester Miscarriage
Study Objective: To compare the time to new pregnancy and pregnancy outcomes in women who received Misoprostol for uterus evacuation versus those treated surgically with dilatation and curettage.
- Trial name
- NCT03570307
- Testing
- medical VS surgical evacuation of the uterus
- Volunteers
- 400 people, healthy volunteers welcome
- Sponsor
- Tel-Aviv Sourasky Medical Center
Induction of Labor Affected Fetus / Newborn
Obesity Study to Assess Induction of Labor
There are more and more pregnant women who are obese. It is very difficult for obese women to get into labor. That is why when women are obese, half are likely to need a Cesarean delivery(C-section).
- Trial name
- Obtainable (NCT03796416)
- Testing
- Misoprostol
- Volunteers
- healthy volunteers welcome
- Sponsor
- University of Maryland, Baltimore
Maternal-Fetal Relations, Microcephaly
Fetal and Maternal Head Circumference During Pregnancy in Israeli Population
In this study, measurements of fetal and maternal head circumference will be collected. This data will be presented in table or graph form.
- Trial name
- NCT02510170
- Testing
- no intervention
- Where
- Israel
- Volunteers
- 188 people, healthy volunteers welcome
- Sponsor
- Clalit Health Services
EOS, Pregnancy Related
Breech Pelvimetry by EOS® Technique With Change of Maternal Position and Delivery Route
When a patient presents with a fetus in PS after 36+0SA, after acceptance of participation in the study, pelvimetry with evaluation of the height of the fetal presentation by EOS® system in the upright and sitting position will…
- Conditions
- EOS, Pregnancy Related, Fetus Fetus, Breech Fetal Presentation
- Trial name
- PelviEOS (NCT05224908)
- Testing
- EOS
- Where
- France
- Volunteers
- 90 people, healthy volunteers welcome
- Sponsor
- University Hospital, Clermont-Ferrand
Breastfeeding, Self Efficacy
The Effect of Emotional Freedom Technique on Breastfeeding Success and Self-Efficacy
This study was planned to determine the effect of emotional freedom technique (EFT) on breastfeeding success and self-efficacy in primiparous women in the early postpartum period who had a cesarean delivery.
- Conditions
- Breastfeeding, Self Efficacy, Cesarean Delivery Affecting Fetus, First Birth
- Trial name
- NCT06199245
- Testing
- emotional freedom technique experimental group
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Medipol University
Fetal Cardiac Disorder
Fetal Cardiac Function Evaluation With aCMQ-Strain Fetal (STRAIN)
To assess whether the aCQM-Strain ultrasound method allows a good analysis of fetal cardiac function. Establish normality parameters and compare it with fetuses with risk factors of cardiac dysfunction.
- Trial name
- STRAIN (NCT03536000)
- Testing
- Fetal echocardiography using the aCMQ-Strain method
- Volunteers
- 250 people, healthy volunteers welcome
- Sponsor
- Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau
Low Birthweight, Preterm Birth
Enhancing Nutrition and Antenatal Infection Treatment for Maternal and Child Health in Ethiopia
The ENAT study will test the impact of packages of antenatal interventions to enhance maternal nutrition and manage pregnancy infections on the outcomes of infant birth size, gestational length, and infant growth in the first 6…
- Conditions
- Low Birthweight, Preterm Birth, Maternal; Malnutrition, Affecting Fetus, Sexually Transmitted Diseases
- Trial name
- ENAT (NCT04171388)
- Testing
- Azithromycin 500 mg, Multiple Micronutrient or Fortified Balanced Energy Protein Supplement, Enhanced Infection Management Package (EIMP)
- Volunteers
- healthy volunteers welcome
- Sponsor
- Brigham and Women's Hospital
Labor; Forced or Induced, Affecting Fetus or Newborn, Labor Onset and Length Abnormalities
Clinical Evaluation of Cervical Ripening in the Outpatient Setting
A randomized controlled trial of mifepristone 200mg vs balloon catheter for cervical ripening.
- Trial name
- NCT04271722
- Testing
- Cervical ripening
- Where
- Portugal
- Volunteers
- 101 people, healthy volunteers welcome
- Sponsor
- Centro Hospitalar Lisboa Norte
Nephropathy
Amniotic Biomarkers for the Prediction of Postpartum Renal Function.
The discovery of antenatal bilateral renal anomaly poses an essential question: can we predict postnatal renal function? Ultrasound is insufficiently precise to predict postnatal renal function evolution.
- Trial name
- BIOMAN (NCT02675686)
- Where
- 31 sites in France
- Volunteers
- 358 people, healthy volunteers welcome
- Sponsor
- University Hospital, Toulouse
Previous; Cesarean Section, Cicatricial, Complicating Pregnancy or Childbirth, Affecting Fetus or Newborn, Prelabor Rupture of Membranes
Balloon Induction of Labor in PROM for TOLAC
A prospective randomized controlled trial to evaluate the safety and efficacy of labor induction with a double balloon catheter (Atad Ripener Device) in women desiring TOLAC (trial of labor after cesarean) with PROM (pre labor…
- Trial name
- BILROM-TOLAC (NCT03399266)
- Testing
- Double Balloon catheter for induction of labor
- Where
- Israel
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- Soroka University Medical Center
Induction of Labor Affected Fetus / Newborn
Nitroglycerin Skin Patches for Facilitating Cervical Ripening: A Randomized Controlled Trial
This study aims to establish the efficacy of transdermal glyceryl trinitrate as a nitric oxide donor in addition to dinoprostone for induction of cervical ripening in the third trimester through progression in the Bishop's score…
- Trial name
- NCT03320187
- Testing
- Nitroderm TTS, Dinoprostone
- Where
- Egypt
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Ain Shams Maternity Hospital
Labor; Forced or Induced, Affecting Fetus or Newborn
The Effects of Increased IV Hydration on Nulliparous Women Undergoing an Induction of Labor
The objective of this study is to compare the effects of intravenous fluid rate on the course of labor in nulliparous patients who are undergoing labor induction and have an unfavorable cervix.
- Trial name
- NCT02989571
- Testing
- Intravenous normal saline administered at 250ml/hr, Intravenous normal saline administered at 125ml/hr
- Where
- United States
- Volunteers
- 180 people, healthy volunteers welcome
- Sponsor
- MemorialCare Health System