Parental Attitudes in Invitro Fertilization
Sponsor
Aljazeera Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT04126109
Collaborator
Cairo University (Other)
400
1
14
28.6
Study Details
Study Description
Brief Summary
The relationship between revelation of mode of conception and child behavior is not known
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
start of assisted reproductive techniques over the past 25 years made many otherwise infertile couples to become parents to genetically related children.
Study Design
Study Type:
Observational
Anticipated Enrollment
:
400 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Parental Reports Toward in Vitro Fertilization
Actual Study Start Date
:
Jan 1, 2019
Anticipated Primary Completion Date
:
Feb 1, 2020
Anticipated Study Completion Date
:
Mar 1, 2020
Outcome Measures
Primary Outcome Measures
- The number of women who got pregnant that will tell others by that [within one year]
The number of women who got pregnant that will tell others by that method
Eligibility Criteria
Criteria
Ages Eligible for Study:
20 Years
to 44 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
- Parents who were enrolled in ICSI and pregnancy occurred
Exclusion Criteria:
- ICSI with no pregnancy
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Algazeerah | Giza | Egypt |
Sponsors and Collaborators
- Aljazeera Hospital
- Cairo University
Investigators
- Principal Investigator: Mahmoud Alalfy, PhD, Algezeera hospitaland National Research Centre ,Egypt
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Aljazeera Hospital
ClinicalTrials.gov Identifier:
NCT04126109
Other Study ID Numbers:
- In vito fertilizaion
First Posted:
Oct 15, 2019
Last Update Posted:
Oct 15, 2019
Last Verified:
Oct 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: