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Completed

NCT Number: NCT04665232

Immunomodulatory Effects of Subcutaneous Progesterone in Patients Affected by Autoimmune Diseases

This study evaluates the immunomodulatory effects of subcutaneous progesterone in patients undergoing IVF by determination of anti-nuclear antibodies (ANA),extractable nuclear antigen antibodies (ENA),anti- neutrophil cytoplasmic antibodies(ANCA),anti-DNA antibodies, anti-cardiolipin antibodies (ACA),Lupus anticoagulant antibodies (LAC) and C3 and C4 fractions of complement on the day of beta hCG dosage and during the eigth week of gestation.

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Key information

Age range

18 year–42 year

Sex eligibility

Female

Study type

Observational

Primary location

Assunta Iuliano

Potenza, 85100, Italy

About this study

The aqueous progesterone preparation for s.c. injection is the first systemic progesterone of its kind for the provision of luteal phase support (LPS) in patients undergoing IVF.

The the high solubility and rapid absorption of the new preparation are enhanced using cyclodextrins that are starch residues with no therapeutic activity and with a particular molecular structure that closely resembles a 'cap'.

Once absorbed after injection, the progesterone molecule is immediately dissociated from its cyclodextrin 'cap', remaining free in the circulation as if produced endogenously by the ovaries.

In comparison to progesterone-in-oil preparation, the new aqueous solution administered by s.c.route resulted in a 3 fold higher and more rapid progesterone peak serum concentrations.

The immunomodulating effects of progesterone are mediated outside of the pelvic cavity, on the peripheral cell of the immune system. For this reason only the injection procedure has this advantage Furthermore, the faster absorption rate and the higher peak serum concentration should increas the systemic immunomodulatory effect of subcutaneous progesterone compared to the vaginal and intramuscular administration

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Infertile patients affected by autoimmune diseases undergoing IVF

Exclusion criteria

  • infertile patients without autoimmune diseases, fertile patients affected by autoimmune diseases

Treatment and study plan

aqueous subcutaneous progesterone

Drug

25 mg/die of aqueous subcutaneous progesterone from the day of oocytes retrieval for two weeks.

Primary outcomes

  1. Pregnancy Rate percentage, Implantation Rate percentage, Live Birth Rate percentage

    Time frame: 12 mounths

    number of pregnancies / 100 embryotransfer, number of implanted embryos/ number of embryos trafsferred, number of live birth

Sponsors and collaborators

Lead sponsor

San Carlo Public Hospital, Potenza, Italy

Other

Registry information

Official study title

Immunomodulatory Effects of Subcutaneous Progesterone in Patients Undergoing IVF Affected by Autoimmune Diseases

Important dates

Study start
2014
Primary completion
2017
Study completion
2017
First posted
Dec 11, 2020
Registry last updated
May 28, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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