Clinical Trials Directory

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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

TypeNameDescription
DRUGGranulocyte colony-stimulating factor and platelet-rich plasma groupAntagonist 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.
OTHERControl groupAntagonist 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.