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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04510870
Other study ID # FI028.DEX001.2019
Secondary ID 2019-002040-24KL
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date August 17, 2020
Est. completion date February 28, 2022

Study information

Verified date August 2020
Source Dextra Fertility Clinic
Contact Annika Tulenheimo-Silfvast, M.D.
Phone +358503507991
Email annika.tulenheimo-silfvast@fimnet.fi
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Iron deficiency may play a critical role in human infertility, oocyte quality and may even play a role in endometrial receptivity. By correcting iron deficiency, low ferritin values, in infertile women with intravenous iron supplementation, embryo quality and pregnancy rates may improve.

The main objective is to evaluate the effect of intravenous iron supplementation on embryo quality (number of good quality blastocysts).

Randomized, double blind, parallel group, cross-over study of ferric carboxymaltose compared to placebo (NaCl infusion).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 62
Est. completion date February 28, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 42 Years
Eligibility Inclusion Criteria:

- Patient's 18 to 42 years and in full consent

- Ferritin = 30 ug/l

- Anti-mullerian hormone (AMH) > 1ug/l

- Planned for IVF/ ICSI treatment

- Diagnosis for treatment: tubal factor, male factor or unexplained infertility (NUD)

Exclusion Criteria:

- Endometriosis

- Poor responder

- Inflammatory bowel disease (IBD), colitis ulcerosa

- Rheumatoid arthritis

- Renal insufficiency

- Cardiac insufficiency

- Body Mass Index (BMI) over 35

- Known hypersensitivity to the active substance, to ferric carboxymaltose or any of its excipients, or to other parental iron products

- Clinical evidence of iron overload or disturbances in the utilization of iron

- use of atosiban or filgrastim during stimulation or embryo transfer

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ferric Carboxymaltose Injection
Infusion prior the start of IVF/ICSI cycle. Dosing according to the summary of product characteristics (SmPC) chart. Placebo infusion before frozen embryo transfer if needed.
NaCl infusion
Placebo infusion prior the start of IVF/ICSI cycle. Ferric Carboxymaltose infusion before frozen embryo transfer if needed. Dosing according to the summary of product characteristics (SmPC) chart.

Locations

Country Name City State
Finland Dextra Fertility Clinic Helsinki

Sponsors (1)

Lead Sponsor Collaborator
Dextra Fertility Clinic

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Other endometrial thickness difference of endometrial thickness in mm compared at the day of infusion and the day of embryo transfer 1 month after infusion, at the time of embryo transfer
Primary Number of good quality blastocysts good quality blastocyst are defined as blastocyst, which are transferable or may be frozen day 5-7 after oocyte pick up
Secondary blastulation rate number of blastocysts /fertilized oocyte day 5-7 after oocyte pick up
Secondary ongoing pregnancy/ pregnancy rate ongoing pregnancy at 12 weeks of gestation/ positive pregnancy test (%) 10 weeks after oocyte pick up,at oocyte pick up it counted to be 2 weeks of gestation.
Secondary mature oocyte rate number of mature oocytes / total number of oocytes (%) 1 day after oocyte pick up
Secondary fertilization rate number of fertilized oocytes/total number of oocytes (%) 1 day after oocyte pick up
Secondary implantation rate number of attached embryos/ embryo transfer (%) 5 weeks after embryo transfer
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