Induction of Labor Clinical Trial
Official title:
The Use of Castor Oil for Induction of Labour in Women With Previous Caesarean Delivery: a Randomized Controlled Trial
Nowadays, more and more women embark on pregnancy with previous Caesarean scar. One in five pregnancies requires induction of labour. The use of non-pharmacological methods (methods without using medication) has been gaining popularity for women who are not good candidates, such as women with previous Caesarean scar, for induction with medications such as prostaglandin. Labour induction with prostaglandin carries a higher risk of uterine rupture and thus it is not routinely offered to women with previous Caesarean delivery in Cairo University Hospital. Non-pharmacological methods of induction of labour appear to be safe in women with previous Caesarean delivery. However, various methods are available and the efficacy among them remain in doubt.
In Cairo University Hospital, castor oil, which is a type of induction methods, is routinely offered to women with previous Caesarean delivery who require induction of labor. However, castor oil may not exert its labor induction effect immediately and the delivery may be delayed by up to 8 days. This may render a proportion of women resort to repeated Caesarean section for failed induction. Castor oil is traditionally given by midwives in order to induce labor. The investigators are intent to recruit 70 healthy pregnant women with a history of previous one cesarean section and with no contraindication to trial of labor after cesarean . Women will be randomly and blindly divided into equal-sized intervention group and control group. Intervention group will be given a single dose 60 mL of castor oil in 140 mL of orange juice, while control group will be given a placebo with similar texture. Primary outcomes to be tested are the percentage of women entering active labor within 24 hours of castor oil or placebo administration and the number of successful vaginal deliveries after cesarean. ;
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 |
NCT04529837 -
Ultrasound Assessment of DILAPAN-S
|
||
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 |