Prolutex in Frozen Embryo Transfer Cycles At the Blastocyst Stage (PROGEX)

IBSA

Status and phase

Completed

Phase 2

Conditions

Infertility

Treatments

Drug: Progesterone Vaginal Product

Drug: Progesterone subcutaneous

Study type

Interventional

Funder types

Industry

Identifiers

NCT03701490

18E-Prg06

Details and patient eligibility

About

The objective of this proof of concept clinical trial is to evaluate the impact of two different progesterone treatments for endometrial preparation (25 mg/twice-a-day, subcutaneous injection, and 200 mg/three times a day, vaginal administration) on the clinical pregnancy rate in women undergoing frozen embryo transfer (FET) at blastocyst stage.

Enrollment

213 patients

Sex

Female

Ages

18 to 49 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Women attending the clinics to undergo a frozen blastocyst embryo transfer, having given written informed consent, with the following characteristics:
18-49 years of age for subjects undergoing ET with donated oocytes (both inclusive);
18-37 years of age for subjects undergoing ET with autologous oocytes (both inclusive);
BMI <32 kg/m2;
Adequate endometrium preparation (Endometrial thickness > 7 mm) and E2 levels ( >100 pg/ml) on the day progesterone treatment is started;
P4 levels <1.5 ng/ml on the day progesterone treatment is started;
Transfer of 1 or 2 frozen embryos at blastocyst stage
Transfer of frozen embryos of quality A and/or B according to Gardner criteria1;
Semen from ejaculation either from the partner or from a bank
≤ 3 previous ET (frozen and fresh) with no pregnancy
Normal uterine cavity (i.e. no polyp or protruding sub-mucosal fibroid).

Exclusion criteria

Presence of functional follicles > 10 mm of diameter on the day progesterone treatment is started;
Intramural uterine fibroids that distort the uterine cavity or polyps >1 cm;
Stage III or IV endometriosis (endometriomas);
Hydrosalpinx;
Pregnancy or lactation
Malformations of the sexual organs incompatible with pregnancy;
Patients affected by pathologies associated with any contraindication of being pregnant;
Known allergy to progesterone preparations or their excipients;
Uncontrolled adrenal or thyroid dysfunction;
Undiagnosed vaginal haemorrhage;
History of, or current arterial disease;
Patients with hepatic impairment;
HIV, Hepatitis B Virus or Hepatitis C Virus seropositive;
Neoplasias (current) or history of neoplasia that may be responsive to progesterone;
High grade cervical dysplasia;
Active thrombophlebitis or thromboembolic disorders, or a history of hormone-associated thrombophlebitis or thromboembolic disorders;
Currently dependent on alcohol, drugs or psychotropic drugs
History of recurrent pregnancy loss defined as 3 or more spontaneous miscarriages wherein pregnancy developed to a minimum of a gestational sac on transvaginal ultrasonography;
Participation in a concurrent clinical trial or another trial within the past 2 months;
Use of concomitant medications that might interfere with the study evaluation: hormonal treatments other than those used in the study, except thyroid hormones.