CIRCAPRO: The Circadian Variability of Serum Progesterone During the Day of a Frozen Embryo Transfer

Sponsor
Universitair Ziekenhuis Brussel (Other)
Overall Status
Recruiting
CT.gov ID
NCT05511272
Collaborator
(none)
44
1
1
4.6
9.6

Study Details

Study Description

Brief Summary

Serum progesterone levels will be evaluated at four different time points during the day of an artificially prepared frozen embryo transfer cycle (HRT FET cycle) and a modified natural cycle frozen embryo transfer cycle (mNC FET cycle) (at 08:00, 12:00, 16:00 and 20:00).The pairwise percentage differences in serum progesterone levels for each patient will be calculated. The intra-day variability of progesterone will be analyzed using mixed models. Pregnancy outcomes will also be assessed.

Condition or Disease Intervention/Treatment Phase
  • Biological: blood test
N/A

Detailed Description

In the HRT FET, estradiol valerate (Progynova) will be administered for endometrial preparation. If the endometrial thickness will be ≥ 6,5 mm during an ultrasound scan planned following an initial period of estrogen priming, micronized vaginal progesterone will be started (Utrogestan 800 mg/d). The transfer of a single blastocyst will be performed on the 6th day of progesterone administration. In a modified NC FET, there is no intake of medication but endocrine and ultrasound monitoring during the proliferative phase. Ovulation trigger with hCG will be considered when a dominant follicle between 16 and 20 mm will be observed and when the endometrial thickness will be ≥ 6,5 mm. The transfer of a single blastocyst will take place on the 7th day after hCG injection.

Serum progesterone levels will be evaluated at four different time points during the day of an artificially prepared frozen embryo transfer cycle (HRT FET cycle) and a modified natural cycle frozen embryo transfer cycle (mNC FET cycle) (at 08:00, 12:00, 16:00 and 20:00). Pairwise percentage differences in serum progesterone levels for each patient will be calculated. The intra-day variability of progesterone will be analyzed using mixed models. Pregnancy outcomes will also be assessed.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
44 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Circadian Variability of Serum Progesterone During the Day of a Frozen Embryo Transfer in an Artificially Prepared Cycle and in a Modified Natural Cycle
Actual Study Start Date :
Jul 14, 2022
Anticipated Primary Completion Date :
Nov 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Frozen embryo transfer cycle

Patients who will undergo a frozen embryo transfer in the modified natural cycle and in an artificially prepared cycle will be included

Biological: blood test
four blood samples will be withdrawn from the participants during the day of their frozen embryo transfer cycle

Outcome Measures

Primary Outcome Measures

  1. The existence of circadian variability of serum progesterone during the day of a frozen embryo transfer [the day of the embryo transfer (from 8 am to 8 pm)]

    To evaluate if there is significant variability in circadian level of serum progesterone on the day of an artificially prepared frozen embryo transfer cycle and during the day of a modified natural frozen embryo transfer cycle

Secondary Outcome Measures

  1. Pregnancy outcomes after the frozen embryo transfer [from the day of the embryo transfer to 12 weeks of pregnancy]

    To evaluate the Clinical pregnancy rate (CPR) in patients who underwent HRT FET or mNC FET. CPR is defined as a pregnancy documented by ultrasound at 6-8 gestational weeks that showed a gestational sac in the uterus

  2. The critical progesterone threshold to optimize pregnancy outcomes [from the day of the embryo transfer to 12 weeks of pregnancy]

    To evaluate the critical threshold of serum progesterone on the day of the FET below which pregnancy rates are significantly lower

  3. The assessment of serum progesterone on the day of frozen embryo transfer [the day of the embryo transfer (from 8 am to 8 pm)]

    To study when is the best moment to measure serum progesterone on the day of FET

  4. Pregnancy outcomes after the frozen embryo transfer [from the day of the embryo transfer to 7 weeks of pregnancy]

    To evaluate the on going pregnancy rate (OPR) in patients who underwent HRT FET or mNC FET. OPR is defined as a viable pregnancy at the ultrasound taken at 12 weeks of gestation that shows the presence of fetal heartbeat

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age ≥ 18 and ≤ 40 years old

  • BMI ≥ 18.5 and ≤ 25,9 kg/m2

  • The patient will undergo a hormone replacement therapy frozen embryo transfer cycle (HRT FET) or a modified natural cycle frozen embryo transfer cycle (mNC FET) according to the standard clinical practice in Brussels IVF

  • In the HRT FET cycle the patient will be administered estradiol valerate and 6 days of micronized vaginal progesterone before the embryo transfer

  • Adequate endometrial pattern (triple layer) and thickness (>6.5 mm) at the moment of planning of the transfer

  • Single blastocyst embryo transfer

  • Signed informed consent

  • Non-smokers

Exclusion Criteria:
  • Age > 40 (women > 40 years old demonstrated an enhanced rate of absorption of progesterone using vaginal tablets compared to younger patients)

  • BMI ≥ 26 (serum progesterone levels on the day of embryo transfer are lower in overweight and obese women compared to those with normal weight)

  • Patients who need to take vaginal estradiol valerate during the HRT FET cycle

  • Intake of any experimental drug or any participation in any other clinical trial within 30 days prior to study start

  • Mental disability or any other lack of fitness, in the investigator's opinion, to preclude subjects in or to complete the study.

  • Current or recent substance abuse, including alcohol and tobacco (patients who stopped tobacco usage at least 3 months prior to screening visit would be allowed)

  • Refusal or inability to comply with the requirements of the study protocol for any reason, including scheduled clinic visits and laboratory tests.

  • Embryo transfer after IVM cycle, PGT or oocyte acceptance

  • Uterine pathologies (fibroids, polyps, chronic endometritis), uterine malformations (septum, Mullerian malformation) and hydrosalpinx

Contacts and Locations

Locations

Site City State Country Postal Code
1 Brussels IVF Brussel Jette Belgium 1090

Sponsors and Collaborators

  • Universitair Ziekenhuis Brussel

Investigators

  • Principal Investigator: Christophe Blockeel, MD, Universitair Ziekenhuis Brussel

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Universitair Ziekenhuis Brussel
ClinicalTrials.gov Identifier:
NCT05511272
Other Study ID Numbers:
  • 1432022000124
First Posted:
Aug 22, 2022
Last Update Posted:
Aug 22, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Aug 22, 2022