Last reviewed · How we verify
NCT02651285
G-CSF Supplemented Medium for IVF Embryo Culture in Patients Undergoing IVF
Phase 4 trial testing G-CSF medium in Infertility in 180 participants. Status unknown.
1 December 2016
Quick facts
| Lead sponsor | Centre for Endocrinology and Reproductive Medicine, Italy |
|---|---|
| Phase | Phase 4 |
| Status | Status unknown |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Enrollment | 180 |
| Start date | 1 January 2016 |
| Primary completion | 1 December 2016 |
| Estimated completion | 1 March 2017 |
| Sites | 1 location across Italy |
Drugs / interventions tested
- G-CSF medium
- Control
Conditions studied
- Infertility — all drugs for Infertility →
- Embryo Development — all drugs for Embryo Development →
- IVF — all drugs for IVF →
Sponsor
Centre for Endocrinology and Reproductive Medicine, Italy — full company profile →
Who can join
Adults 20 to 38, female only, with Infertility or Embryo Development. Patients with the condition only — healthy volunteers not accepted.
What's being measured
Primary outcomes are the specific endpoints the trial is designed to prove or disprove.
-
pregnancy rate
Time frame: 12 months
The number of patients become pregnant after IVF where G-CSF medium is used divided for the number of patients treated -
implantation rate
Time frame: 12 months
The number of embryos implanted after IVF where G-CSF medium is used divided for the number of embryos transferred
Sponsor's own description
The purpose of this study is to determine whether in Assisted Reproductive Technologies the use of culture medium supplemented with G-CSF, a growth factor working on stem cells, may improve the embryo implantation and pregnancy rate in infertile patients undergoing IVF cycles.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
GM-CSF (granulocyte macrophage colony-stimulating factor) supplementation in culture media for women undergoing assisted reproduction.
Armstrong S, MacKenzie J, Woodward B, Pacey A, et al · · 2020 · cited 10× · PMID 32672358 · DOI 10.1002/14651858.cd013497.pub2
Verify or expand the search:
- PubMed search for NCT02651285
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Centre for Endocrinology and Reproductive Medicine, Italy trials
Trials by the same sponsor.
- NCT06641440 — Treatment With Prednisone of Women With RPL or RIF Positive to Antithyroid Antibodies and Embryotoxicity Test · Phase 4 · completed
- NCT03421639 — Aromatase Plus GnRH Analogue Versus GnRH Analog Alone in Adenomyosis · Phase 4 · unknown
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02651285 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Centre for Endocrinology and Reproductive Medicine, Italy
- Last refreshed: 7 January 2016
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02651285.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing