Trials / Unknown
UnknownNCT04411212
G-CSF and PRP in Patients With Recurrent Implantation Failure
Granulocyte Colony-stimulating Factor and Platelet-rich Plasma Group in Patients With Recurrent Implantation Failure
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 112 (estimated)
- Sponsor
- Riyadh Fertility and Reproductive Health center · Academic / Other
- Sex
- Female
- Age
- 1 Year – 35 Years
- Healthy volunteers
- Not accepted
Summary
The aim of this randomized controlled trial is to determine whether granulocyte colony-stimulating factor and platelet-rich plasma can be used to enhance the IVF-ET outcomes in patients with recurrent implantation failure
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Granulocyte colony-stimulating factor and platelet-rich plasma group | Antagonist protocol is used . Oocyte retrieval under transvaginal ultrasound guidance is performed 34 to 36 hours after HCG administration. Autologous platelet-rich plasma is prepared from the blood using the two step centrifuge process. Under ultrasound guidance and complete aseptic procedures, 1 ml of the PRP is infused inside the uterus while performing the mock embryo transfer. Moreover, G-CSF (Filgrastim®, 300μg/0.5ml) is injected subcutaneously. G-CSF is injected weekly until the 12th gestation week or negative pregnancy test. |
| OTHER | Control group | Antagonist protocol is used . Oocyte retrieval under transvaginal ultrasound guidance is performed 34 to 36 hours after HCG administration. Mock embryo transfer is performed without injecting anything inside the uterus. |
Timeline
- Start date
- 2020-05-28
- Primary completion
- 2020-12-31
- Completion
- 2021-03-31
- First posted
- 2020-06-02
- Last updated
- 2020-06-02
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT04411212. Inclusion in this directory is not an endorsement.