Induction of Labor Clinical Trial
Official title:
Longitudinal Ultrasound Evaluation of Dilapan-S During Cervical Ripening
The goal of this observational prospective study is to assess the change in Dilapan-S rod diameters using transvaginal ultrasound over a period of 12 hours in term women undergoing induction of labor.
On admission for induction, study participants assigned to each group underwent continuous cardiotocography for 20 minutes prior to placement of the Dilapan-S rods (rod size: 4 x 65mm). Placement of the Dilapan-S rods was limited to three physicians with the majority placed by the primary investigator. Placement was completed in a sterile manner under direct visualization and in accordance with the manufacturer's guidelines. The number of rods placed varied per individual and was based on the discretion of the physician. Each participant allocated to the Dilapan-S with saturated gauze group received placement of one, 4x4 inch gauze saturated with 10 cc of normal saline and placed at the level of the external os. Immediately after placement of the Dilapan-S rods, the study participant was asked to complete a patient satisfaction survey. Pre-specified transvaginal ultrasound assessment was performed at hours 3, 6, 8, and 12 post Dilapan-S placement using a GE Voluson E10 machine with a transvaginal GE RIC 5-9D transducer. Performance of the ultrasound evaluation was limited to the primary investigator and two co-authors of the study. After completion of the 12-hour ultrasound, the Dilapan-S rods and gauze, if used, were removed as per the manufacturer's instructions. The participant was then asked to complete a post Dilapan-S patient satisfaction survey. ;
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 | |
Active, not recruiting |
NCT06056141 -
Induction of Labour at Term With Low Dose Oral Misoprostol Versus a Foley Catheter
|
Phase 4 | |
Completed |
NCT02477085 -
Methods of Labor Induction and Perinatal Outcomes
|
||
Completed |
NCT03138252 -
Study of the Effectiveness of Cervical Ripening Balloon With and Without Oxytocin
|
Phase 3 | |
Completed |
NCT02098421 -
Foley Labor Induction Trial at Term and in PROM
|
Phase 1 | |
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 |