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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03479879
Other study ID # AS1731
Secondary ID
Status Completed
Phase Phase 2/Phase 3
First received
Last updated
Start date March 21, 2018
Est. completion date December 20, 2018

Study information

Verified date January 2019
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare the effectiveness of estradiol pretreatment with misoprostol and vaginal misoprostol alone in induction of second trimestr miscarriage.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date December 20, 2018
Est. primary completion date December 20, 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Maternal age more than 18 years old (age of legal consent).

- Gestational age between 12-26 weeks.

- Hb level > 10 g/dL.

- BMI between 25 kg/m2 and 35 kg/m2.

- Missed abortion.

- Living fetus with multiple congenital malformations incompatible with life.

- PPROMS with drained liquor and parents are consenting for termination of pregnancy.

Exclusion Criteria:

- Maternal age less than 18 years old.

- Gestational age less than 12 weeks or more than 26 weeks.

- Hb level < 10 g/dL.

- Scared uterus (previous myomectomy - cesarean section - hysterectomy and ruptured uterus).

- Polyhydramnios.

- Anencephaly.

- Fibroid uterus.

- BMI less than 25 kg/m2 and more than 35 kg/m2.

- Coagulopathy.

- Previous attempts for induction of abortion in the current pregnancy.

- Allergy to misoprostol or estradiol.

- Placenta previa.

- Medical disorder that contraindicate induction of abortion (e.g. heart failure).

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Estradiol
Estradiol
Placebo Oral Tablet
Placebo
Misoprostol
Misoprostol

Locations

Country Name City State
Egypt Ain Shams University Maternity Hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Duration of induction of abortion 24 hours
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