Induction of Labor Clinical Trial
Official title:
Induction of Labour at Term With Low Dose Oral Misoprostol Versus a Foley Catheter: a Multicentre Randomised Controlled Trial
Comparison of efficacy and safety of low-dose oral Misoprostol versus folley catheter for preinduction in women with an immature cervix at term.
Open-label randomised trial in 2 hospitals in the Almaty,Kazakhstan. Women with a term singleton pregnancy in cephalic presentation, an unfavourable cervix, intact membranes, and without a previous caesarean section will be randomly allocated to 2 groups: 1 group -cervical ripening with 25 μg oral misoprostol once every 2 hour, 2 nd group- a 30 mL transcervical Foley catheter. The primary outcome will be vaginal delivery within 24 hours(to evaluate effectiveness) and secondary outcoms 1-5-min Apgar score and hospitalization in ICU, hyperstimulation frequency and hemorrage (for evaluating safety) ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT01127581 -
Efficacy & Safety Study Comparing Misoprostol Vaginal Insert (MVI) Versus Dinoprostone Vaginal Insert (DVI) for Reducing Time to Vaginal Delivery
|
Phase 3 | |
| Completed |
NCT01139801 -
Cervical Ripening for Induction of Labor: Misoprostol Versus Oxytocin in Conjunction With Foley Balloon
|
N/A | |
| Active, not recruiting |
NCT06324279 -
Cervical Sliding Sign to Predict Outcome of Induction of Labor
|
||
| Recruiting |
NCT05864326 -
Heated Saline in Cervical Balloon for Labor Induction, a RCT
|
N/A | |
| Completed |
NCT04529837 -
Ultrasound Assessment of DILAPAN-S
|
||
| Completed |
NCT02477085 -
Methods of Labor Induction and Perinatal Outcomes
|
||
| Completed |
NCT02098421 -
Foley Labor Induction Trial at Term and in PROM
|
Phase 1 | |
| Completed |
NCT03138252 -
Study of the Effectiveness of Cervical Ripening Balloon With and Without Oxytocin
|
Phase 3 | |
| Recruiting |
NCT01720394 -
Efficacy of Induction of Labor on Term Using a Double Balloon Catheter Compared to Dinoprostone Vaginal-insert
|
Phase 4 | |
| Completed |
NCT00451308 -
Induction of Labor With a Foley Balloon Catheter: Inflation With 30ml Compared to 60ml
|
Phase 4 | |
| Not yet recruiting |
NCT05511727 -
Use of Single Versus Double Foley's Catheter in Pre-induction Cervical Ripening
|
N/A | |
| Recruiting |
NCT02762942 -
Comparison of Vaginal Misoprostol Plus Supracervical Balloon Versus Vaginal Misoprostol Alone for Induction of Labor
|
Phase 4 | |
| Completed |
NCT01283022 -
Pharmacokinetic (PK) Study of the 200 Microgram (mcg) Misoprostol Vaginal Insert (MVI 200) in Women at Term Gestation (The MVI-PK Study)
|
Phase 2 | |
| Recruiting |
NCT00684606 -
Transcervical Foley Catheter With or Without Oxytocin for Induction of Labor
|
N/A | |
| Recruiting |
NCT05759364 -
The Effect of IV PAPAVERINE 80 mg Prior to Catheter Balloon Insertion on Bishop Score and Pain
|
N/A | |
| Recruiting |
NCT03854383 -
Using Isosorbide Mononitrate in Reducing Time in Induction of Labor in Post Date Women
|
Phase 2 | |
| Completed |
NCT01428037 -
Safety and Efficacy Study of Vaginal Misoprostol for Cervical Ripening and Induction of Labor
|
Phase 3 | |
| Terminated |
NCT03752073 -
Comparison of Two Mechanical Methods of Outpatient Ripening of the Cervix
|
N/A | |
| Recruiting |
NCT03045939 -
Cervical Ripening With the Double Balloon Device for 6 Hours Compared With 12 Hours
|
N/A | |
| Completed |
NCT03976037 -
Buccal Versus Vaginal Misoprostol In Combination With Foley Bulb
|
Early Phase 1 |