Abnormal Menstrual Cycle Clinical Trial
Official title:
The Use of Luteal Support After NC-FET
The investigators are going to examine prospectively the need of luteal support after NC-FET.
Status | Recruiting |
Enrollment | 100 |
Est. completion date | December 2014 |
Est. primary completion date | December 2014 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 39 Years |
Eligibility |
Inclusion Criteria: - Women under 39 years old, regular menstruation going through IVF NC-FET Exclusion Criteria: |
Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care
Country | Name | City | State |
---|---|---|---|
Israel | Wolfson medical center | Holon |
Lead Sponsor | Collaborator |
---|---|
Wolfson Medical Center |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pregnancy rate | We would like to investigate whether there is need for luteal support in NC-FET cycle. | 4 weeks | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02035930 -
Effect of Dexmedetomidine on Bispectral Index and Propofol Requirements During Different Menstrual Cycle
|
Phase 4 |