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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03113097
Other study ID # DAT-055
Secondary ID
Status Completed
Phase N/A
First received April 10, 2017
Last updated April 10, 2017
Start date June 2014
Est. completion date March 2017

Study information

Verified date April 2017
Source Ain Shams University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Women planned to undergo blastocyst-stage embryo transfer after IVF/ICSI were randomized into 2 groups:

- group I: women who had only good-quality embryo transfer.

- group II: women who had both good-quality and poor-quality embryo transfer.

primary outcome was ongoing clinical pregnancy rate


Recruitment information / eligibility

Status Completed
Enrollment 627
Est. completion date March 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

- women undergoing primary IVF/ICSI cycles for tubal factor/unexplained infertility and had blastocyst-stage ET

Exclusion Criteria:

- cleavage-stage ET.

- women who had no good-quality embryos to transfer

- women who had known poor endometrial receptivity

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Embryo transfer
Transfer of different qualities of embryos at blastocyst stage

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Ain Shams University Dar El Teb Institute

Outcome

Type Measure Description Time frame Safety issue
Primary Ongoing clinical pregnancy rate viable intrauterine pregnancy ongoing beyond 12 weeks of gestation 12 weeks
Secondary Biochemical pregnancy rate positive serum hCG 2 weeks after ET
Secondary Clinical pregnancy rate sonographic detection of viable intrauterine gestational sac 4 weeks after ET
Secondary Multiple pregnancy rate No. of intrauterine gestational sacs 4-6 weeks after ET
Secondary Ectopic pregnancy rate Extrauterine pregnancy 6 weeks after ET
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