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G-CSF and Assisted Reproductive Techniques outcomes in repeated implantation failures

G-CSF and Assisted Reproductive Techniques outcomes in repeated implantation failures

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013063011653N2
Enrollment
100
Registered
2013-07-16
Start date
2013-07-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Infertility. In vitro fertilization

Interventions

Intervention 1: In Intervention group 1cc(300)microgram Granulocyte-colony stimulating factor will be injected in to uterine cavity through vagina. Intervention 2: In Control group 1cc normal salin wi
Treatment - Drugs
In Intervention group 1cc(300)microgram Granulocyte-colony stimulating factor will be injected in to uterine cavity through vagina.
In Control group 1cc normal salin will be injected in to uterine cavity through vagina.

Sponsors

Avicenna Infertility Treatment Center
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 38 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: ART failure>3; Age:20-38; Normal karyotype and uterus anatomy; Do not have infection,endocrine and immune and coagulation disorders ,thrombophilia; Normal TSH,LH,FBS; FSH<10 TPO<500; Negative lupus anti coagulant; Negative Toxoplasma,CMV,Rhubella; Normal Factor 5leiden,factor2 prothrombin,protein C, Pr S Exclusion criteria:Azoospermia with negative testis biopsy; Egg donation; Suffering from cancer

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical pregnancy. Timepoint: After intervention. Method of measurement: Gestational Sac in sonography.

Secondary

MeasureTime frame
Chemical pregnancy. Timepoint: After intervention. Method of measurement: HCG.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Sara Mokhtar

Avicenna Infertility treatment center

smkhtr@yahoo.com+98 21 2261 7930

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026