Supervision of Pregnancy Resulting From In-vitro Fertilization Clinical Trial
— PLUSOfficial title:
Optimal Planning of a Day 3 Cryopreserved(Frozen)-Thawed Embryo Transfer in a Natural Cycle With hCG Administration or After Spontaneous LH Peak?
| NCT number | NCT02145819 |
| Other study ID # | PLUS |
| Secondary ID | |
| Status | Completed |
| Phase | Phase 4 |
| First received | |
| Last updated | |
| Start date | January 2014 |
| Est. completion date | September 2019 |
| Verified date | September 2019 |
| Source | Universitair Ziekenhuis Brussel |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The aim of the study is to determine whether spontaneous LH peak is superior to human chorionic gonadotropin before a transfer of a day 3 frozen embryo.
| Status | Completed |
| Enrollment | 240 |
| Est. completion date | September 2019 |
| Est. primary completion date | September 2019 |
| Accepts healthy volunteers | No |
| Gender | Female |
| Age group | 18 Years to 39 Years |
| Eligibility |
Inclusion Criteria: - Natural cycles, in which a frozen-thawed day 3 embryo is replaced. - Signed informed consent. - Regular cycle (i.e. between 26 and 35 days) - Normal transvaginal ultrasound at screening, without evidence of clinically significant abnormality consistent with finding adequate for ART with respect to uterus and adnexa. - Embryos frozen by vitrification. - Single or dual embryo transfer. Exclusion Criteria: - Known allergic reactions to progesterone products. - Intake of experimental drug within 30 days prior to study start. - Contraindication for pregnancy. - Embryos of women above 39 years of age at the time of embryo freezing. - Recipients of oocyte donation cycles |
| Country | Name | City | State |
|---|---|---|---|
| Belgium | Centre of Reproductive Medicine CRG | Jette | Brussels |
| Lead Sponsor | Collaborator |
|---|---|
| Universitair Ziekenhuis Brussel |
Belgium,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | clinical pregnancy rate | We evaluate the pregnancy, at 7 weeks amenorrhoea. Outcome is clinical pregnancy rate | 7 weeks | |
| Secondary | number of monitoring visits at the clinic per cycle | 7 weeks |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Not yet recruiting |
NCT01608048 -
Transcutaneous Electrical Acupoint Stimulation to Improve Pregnancy Rates for Women Undergoing in Vitro Fertilization
|
N/A |