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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
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04411212
Enrollment
112
Registered
2020-06-02
Start date
2020-05-28
Completion date
2021-03-31
Last updated
2020-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility,Female

Keywords

IVF, Platelet-rich plasma, Granulocyte colony-stimulating factor, Recurrent implantation failure

Brief 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

Interventions

DRUGGranulocyte 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.

OTHERControl 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.

Sponsors

Riyadh Fertility and Reproductive Health center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
1 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

• Patients with history of three or more unsuccessful IVF-ET cycles with at least 2 good quality embryos transferred

Exclusion criteria

* Endometriosis * Uterine anomalies * Asherman syndrome

Design outcomes

Primary

MeasureTime frameDescription
Clinical pregnancy rateFive weeks after embryo transferGestational sac detected by ultrasound examination

Countries

Egypt

Contacts

Primary ContactUsama M Fouda, Prof.
umfrfouda@yahoo.com+0201095401375

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026