Clinical trials: Labour Induction
Fetal Distress
Sildenafil Citrate and Intrapartum Fetal Distress
Induction of labour (IOL) is done for 20% of pregnancies for various maternal and fetal indications and nearly 20% of labour inductions end up in caesarean section.
- Trial name
- NCT04325243
- Testing
- Sildenafil 50 mg
- Where
- Egypt
- Volunteers
- 410 people
- Sponsor
- Assiut University
Medical Induction of Labor Affecting Fetus
Titrated Oral Misoprostol Compared to Vaginal Dinoprostone for Induction of Labor
To test the safety and efficacy of titrated oral misoprostol compared to vaginal dinoprostone for labor induction.
- Trial name
- NCT02036437
- Testing
- Misotac® Sigma Pharmaceutical Industries, Dinoprostone 3 mg
- Where
- Egypt
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- Ain Shams University
Failed Induction of Labor
A Comparison of Transcervical Foley Catheter and Prostaglandins for Induction of Labor at Term
The purpose of this study is to assess the effectiveness and safety of transcervical foley catheter as compared to prostaglandins for preinduction cervical ripening and labor induction in term nulliparous women with unfavorable…
- Trial name
- NCT01317862
- Testing
- Transcervical foley catheter, Prostaglandins
- Where
- South Korea
- Volunteers
- 154 people
- Sponsor
- Seoul National University Hospital
Induction of Labor Affected Fetus / Newborn, Prostaglandins Causing Adverse Effects in Therapeutic Use
Induction of Labor in Term Pregnancies With Unfavourable Cervix
This is a prospective randomized trial comparing two prostaglandin E2 (dinoprostone) agents used for labor induction in pregnant women with term pregnancies and unfavorable cervix.
- Trial name
- RAND (NCT04280874)
- Testing
- Dinoprostone 0.5 MG, Dinoprostone 2 MG/2.5 ML Vaginal Gel/Jelly
- Where
- Croatia
- Volunteers
- 212 people, healthy volunteers welcome
- Sponsor
- Clinical Hospital Merkur
Virtual Reality, Induction of Labor Affected Fetus / Newborn
VR Glasses During Induction of Labour for Pain and Anxiety Relieve
In the current study, The investigators aim is to test the distraction affect of "Virtual Reality" (VR) technology on pain and anxiety in pregnant women who undergo through an induction of labour with an extra-amniotic balloon…
- Conditions
- Virtual Reality, Induction of Labor Affected Fetus / Newborn, Extra Amniotic Balloon
- Trial name
- NCT05187247
- Testing
- Virtual Reality glasses
- Where
- Israel
- Volunteers
- 145 people, healthy volunteers welcome
- Sponsor
- Wolfson Medical Center
Normal Vaginal Delivery
Oral Misoprostol Solution in Comparison to Vaginal Misoprostol in Induction of Labor
Induction of labour at term is a common obstetric intervention. Induction of labour is the artificial initiation of labour before its spontaneous onset for the purpose of delivery of the fetoplacental unit using mechanical or…
- Trial name
- NCT03863392
- Testing
- Misoprostol
- Where
- Egypt
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Ain Shams University
Induction of Labor
Cervical Foley Plus Vaginal Misoprostol for Labor Induction
The purpose of this study is to compare the efficacy of the combination of the supracervical foley bulb and vaginal misoprostol to vaginal misoprostol alone for labor induction.
- Trial name
- NCT01279343
- Testing
- Foley bulb
- Where
- United States
- Volunteers
- 123 people, healthy volunteers welcome
- Sponsor
- Washington University School of Medicine
Birth Weight, Macrosomia, Fetal
Association Between Labor Induction and Birth Weight in Cases of Fetal Macrosomia: The MACROMODA Cohort Study
The rising prevalence fof fetal macrosomia represents a significant challenge in obstetrics, affecting both maternal and neonatal outcomes. Such challenges include complications like perineal tears and postpartum hemorrhage.
- Trial name
- MACROMODA (NCT06198881)
- Where
- 3 sites in France
- Volunteers
- 4,500 people
- Sponsor
- Hospices Civils de Lyon
Induction of Labour
REgistry of MisOprostol 200 µg Vaginal dElivery System
The design of the study is post-marketing, observational, multi-centre and open-label. The study does not provide treatment; only patients to whom misoprostol 200 µg vaginal delivery system (VDS) is prescribed may be included.
- Trial name
- REMOVE (NCT02242214)
- Testing
- Misoprostol
- Where
- Netherlands
- Volunteers
- 106 people
- Sponsor
- Ferring Pharmaceuticals
Cervical Ripening, Induction of Labor
Heated Saline in Cervical Balloon for Labor Induction, a RCT
This study is a single-center, randomized, two-arm, controlled trial, including women requiring cervical ripening during the process Induction of Labor using Balloon catheter (BC).
- Conditions
- Cervical Ripening, Induction of Labor, Unfavorable Cervix, Mechanical Method
- Trial name
- NCT05864326
- Testing
- Warm group, Room temperature group
- Where
- Switzerland
- Volunteers
- 290 people, healthy volunteers welcome
- Sponsor
- Begona Martinez de Tejada
Pregnancy
Induction With Misoprostol: Oral Mucosa Versus Vaginal Epithelium (IMPROVE)
The primary objective of this study is to compare the efficacy and safety of vaginal and buccal misoprostol for women undergoing labor induction at greater than or equal to 37+ 0 completed weeks gestation.
- Trial name
- IMPROVE (NCT02408315)
- Where
- 2 sites in United States
- Volunteers
- 300 people
- Sponsor
- Indiana University
Induction of Labor
Induction of Labor With a Foley Balloon Catheter: Inflation With 30ml Compared to 60ml
The rate of labor induction is rising throughout the United States for a variety of reasons. Medical conditions that lead to increased risk of prolonging the pregnancy to both mother and fetus are not infrequent.
- Trial name
- NCT00451308
- Testing
- Induction of labor with foley balloon - 60cc of saline, Induction of labor with foley balloon with 30cc
- Where
- United States
- Volunteers
- 192 people
- Sponsor
- University of California, San Francisco
Induction of Labor Affected Fetus / Newborn
Dilapan-S® for Induction of Labor The Feasibility Study
This is a prospective feasibility study to investigate Dilapan-S® as an outpatient method of cervical ripening in low risk pregnancies >=39 weeks.
- Trial name
- DILATE (NCT04521062)
- Testing
- Dilapan S
- Where
- United States
- Volunteers
- 22 people, healthy volunteers welcome
- Sponsor
- Albany Medical College
Labour Induction
Vaginally Administered Versus Per Oral Misoprostol in Induction of Labour
The purpose of this study is to investigate the effectiveness and safety of vaginally administered misoprostol (Misodel) versus per orally administered misoprostol (Cytotec) in induction of labour in nulliparous women.
- Trial name
- NCT02539199
- Testing
- Misoprostol, modified-release pessary, Misoprostol, per-oral tablets
- Where
- 5 sites in Finland
- Volunteers
- 270 people
- Sponsor
- Tampere University Hospital
Labor, Induced
The Efficacy of Early Amniotomy for Induction of Labor
The purpose of this clinical trial is to investigate the efficacy of early amniotomy on reducing both the duration of labor and the frequency of dystocia in nulliparous women undergoing an induction of labor.
- Trial name
- NCT00133016
- Testing
- Amniotomy
- Where
- United States
- Sponsor
- University of Pennsylvania
Pregnancy, Induced Labor
Evaluation the Blood Loss in Pregnancies With Misoprostol-induced Labour
The purpose of this study is to evaluate the blood loss in induced vaginal delivery by misoprostol and caesarians section with induction attempt.
- Trial name
- NCT01231126
- Testing
- Misoprostol
- Where
- Brazil
- Volunteers
- 161 people
- Sponsor
- Maternidade Escola Assis Chateaubriand
Failed Induction of Labor
Comparison Between Ultrasonographic Cervical Length and Bishop Score in Preinduction Cervical Assessment
To compare the ultrasonographic cervical length with the Bishop score in determining the administration of prostaglandin for preinduction cervical ripening in nulliparas at term.
- Trial name
- NCT01317706
- Testing
- Assessment of cervical status
- Where
- South Korea
- Volunteers
- 154 people
- Sponsor
- Seoul National University Hospital
Induction of Labor
Methods of Labor Induction and Perinatal Outcomes
Since it is a frequent intervention in Obstetrics, labor induction is rarely evaluated from national population-based cohorts. The study aims to assess the frequency of different induction methods used in France from a…
- Trial name
- MEDIP (NCT02477085)
- Testing
- all women with an induced labor
- Where
- France
- Volunteers
- 3,049 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Obesity, Induction of Labor Affected Fetus / Newborn
Antibiotic Prophylaxis to Prevent Obesity-Related Induction Complications in Nulliparae at Term
Obesity increases the risk of pregnancy complications, including among others puerperal infections and cesarean delivery, and risk rises with increasing body mass index (BMI).
- Trial name
- APPOINT (NCT03801252)
- Testing
- Cefazolin, Azithromycin
- Where
- United States
- Volunteers
- 186 people, healthy volunteers welcome
- Sponsor
- University of Oklahoma
Intrahepatic Cholestasis
Induction of Labor in Intrahepatic Cholestasis of Pregnancy
Induction of Labour in Intrahepatic Cholestasis of Pregnancy (ICP) has become a common procedure in management of ICP to avoid fetal complications.
- Trial name
- ILICP (NCT01381939)
- Volunteers
- 5,000 people
- Sponsor
- Karolinska Institutet