Randomized Clinical Trial for Comparison Of Intravenous Carbeitocin Versus Oxytocin In Management Of Placental Delivery In Second Trimester Interruption

CARBETOCIN FOR PREVENTION OF PLACENTAL RETAINED Clinical Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01827124
• Other study ID #: Ain Shams U
• Status: Recruiting
• Phase: Phase 4
• First received: April 5, 2013
• Last updated: October 7, 2013
• Start date: April 2013
• Est. completion date: December 2013

Study information

• Verified date: April 2013
• Source: Ain Shams University
• Contact: WAFAA UTHMAN AHMED, M.B.CH.B
• Phone: 00201119760754
• Email: WAFAA.UTHMAN[@]YAHOO.COM
• Is FDA regulated: No
• Health authority: Egypt: Institutional Review BoardUnited States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Intravenous Carbetocin is more efficient than intravenous infusion oxytocin in management of placental delivery in 2nd trimester interruption.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 140
• Est. completion date: December 2013
• Est. primary completion date: November 2013
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 16 Years to 50 Years

Eligibility

Inclusion Criteria:

• Age:16-50 years

• Pregnancy duration: 14-24weeks

• Spontaneous abortion or medical induced abortion at 14-24weeks

Exclusion Criteria:

• Age less than 16years and more than 50 years

• Surgical termination

• Placenta previa

• Uterine fibroid

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention

Related Conditions & MeSH terms

• CARBETOCIN FOR PREVENTION OF PLACENTAL RETAINED

Intervention

Drug:
• Carbetocin

• oxytocin

Locations

Country	Name	City	State
Egypt	Ain Shams university maternity hospital department of obstetrics and gynacology	Cairo	Tertiary

Sponsors (2)

Lead Sponsor	Collaborator
Wafaa Uthman Ahmed	Ain Shams Maternity Hospital

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Record duration of spontaneous placental expulsion after delivery of fetus in second trimester interruption		at the time of delivery	Yes
Secondary	Estimation of blood loss in each group by weighing all pads put under the patient after delivery of fetus tell expulsion of placenta( before and after using of pads).		at time of delivery	Yes