| Recruiting | PGE2 Followed by Oxytocin vs Oxytocin in Term PROM (POXY-PROM) NCT07366359 | National Hospital of Obstetrics and Gynecology | N/A |
| Recruiting | Maternal Informing on Labor Induction: Impact on Childbirth Experience NCT07272785 | Turku University Hospital | — |
| Recruiting | Use of Papaverine to Shorten the Second Stage/Duration of Labor in Pregnant Women After Cervical Ripening by D NCT07237880 | Hillel Yaffe Medical Center | N/A |
| Recruiting | Membrane Stripping for Cervical Ripening NCT06591247 | Meir Medical Center | N/A |
| Recruiting | Topical Anesthesia During Catheter Insertion for Cervical Ripening (TOLERANCE) NCT07288021 | Bnai Zion Medical Center | Phase 4 |
| Recruiting | Mifepristone Outpatient Labour Induction NCT05177510 | Chelsea and Westminster NHS Foundation Trust | Phase 2 |
| Completed | Should I Have an Elective Induction? NCT05838313 | University of South Florida | N/A |
| Completed | Impact of Timing of Neuraxial Analgesia on Obstetric, Anesthesiologic and Neonatal Outcomes in Induced Labour NCT06886555 | Fondazione IRCCS Policlinico San Matteo di Pavia | — |
| Completed | 'Extended Balloon Catheter' Labour Induction; a Single Arm Pilot Trial' NCT05885087 | University of Botswana | N/A |
| Completed | Effect of Acidic Vaginal pH on the Efficacy of Dinoprostone for Labor Induction NCT05100264 | Alexandra Hospital, Athens, Greece | N/A |
| Completed | Labor Induction With Oral Versus Vaginal Misoprostol NCT04755218 | University of Texas Southwestern Medical Center | — |
| Completed | Outpatient Labor Induction Using Oral Misoprostol in Norway NCT04746248 | Oslo Metropolitan University | N/A |
| Completed | Early Versus Late Amniotomy During Labor Induction in Women With Bishop's Score of ≥ 6 NCT04731896 | University Tunis El Manar | N/A |
| Completed | Induction of Labour With a Double Balloon Catheter NCT05874024 | Jena University Hospital | — |
| Unknown | Misoprostol for Induction of Labor in Obese Women: Comparison Between 25 and 50 mcg Oral Administration NCT05857059 | Unidade Local de Saúde de Coimbra, EPE | N/A |
| Completed | Prediction of Spontaneous Onset of Labor at Term NCT05109247 | University Hospital, Geneva | — |
| Completed | Comparing Outpatient to Inpatient Cervical Ripening Using Dilapan-S® NCT03665688 | The University of Texas Medical Branch, Galveston | N/A |
| Completed | Labor Induction With a Combined Method (Pharmacologic and Mechanical): Randomized Controlled Trial NCT03928600 | Centro Hospitalar De São João, E.P.E. | N/A |
| Completed | Foley Bulb With Oral Misoprostol for Induction of Labor NCT03407625 | University of Texas Southwestern Medical Center | N/A |
| Completed | Oxytocin Dosage to Decrease Induction Duration NCT03140488 | University of Arizona | Phase 4 |
| Unknown | Efficacy and Safety of Hourly Titrated Misoprostol Versus Vaginal Dinoprostone and Misoprostol for Cervical Ri NCT02902653 | Oihane Lapuente Ocamica | Phase 4 |
| Terminated | Elastography for Evaluating Cervical Maturity in Preparation for Labor Induction at 37 to 42 Weeks of Gestatio NCT02373800 | Centre Hospitalier Universitaire de Nīmes | — |
| Unknown | A Trial of Prostaglandin E2 Tablets Versus Foley Catheter for Labor Induction NCT02486679 | Wolfson Medical Center | Phase 4 |
| Completed | Randomized Controlled Trial: Induction of Labour of Obese Women With Dinoprostone or Single Balloon Catheter NCT01962831 | Saskatchewan Health Authority - Regina Area | N/A |
| Terminated | Prehospital Cervical Ripening Before Induction and the Maternal Experience NCT01641601 | University of California, San Francisco | N/A |
| Completed | Oral Titrated Misoprostol for Induction of Labour NCT00992524 | Instituto Materno Infantil Prof. Fernando Figueira | N/A |
| Completed | 24-Hour Vaginal Dinoprostone Pessary Versus Gel for Labour Induction NCT00843362 | Università degli Studi di Brescia | Phase 4 |
| Withdrawn | The Efficacy of Early Amniotomy for Induction of Labor NCT00133016 | University of Pennsylvania | N/A |
| Completed | Safety/Efficacy Study Comparing the Misoprostol Vaginal Insert to Cervidil for Cervical Ripening and Induction NCT00308711 | Ferring Pharmaceuticals | Phase 3 |
| Completed | Study of Ultrasound Imaging to Predict Time and Outcome in Pregnancies With Induced Labor NCT00465998 | Helse Stavanger HF | — |
| Completed | Recombinant Human Relaxin (rhRlx) in Pregnant Women Scheduled for Induction of Labor NCT00259103 | Corthera, Inc.(formerly BAS Medical, Inc.), a member of the Novartis group of companies | Phase 2 |
| Completed | A Randomized Study on Comparing the Efficacy of Foley Catheter and Extraamniotic Saline Infusion for Labor Ind NCT00366951 | Rush University Medical Center | N/A |
| Completed | A Randomized, Control Trial for Preinduction Cervical Ripening NCT00393731 | The University of Texas Health Science Center, Houston | Phase 2 |
| Withdrawn | Cervical Ripening Before Induction of Labour at Term: a Randomised Comparison of Prostin vs Propess NCT00545194 | Institut National de la Santé Et de la Recherche Médicale, France | Phase 3 |