Effect of Intervention on Progesterone Levels Before Euploid Embryo Transfer in Pregnancy Outcomes.

Sponsor
Institut Universitari Dexeus (Other)
Overall Status
Completed
CT.gov ID
NCT03740568
Collaborator
Fundación Santiago Dexeus Font (Other), Dexeus Clinic Woman (Other)
598
1
2
15.4
38.7

Study Details

Study Description

Brief Summary

Transferring an euploid embryo avoids one of the main reasons of miscarriage and implantation failure (1), overcoming confounding factors such as embryo ploidy or maternal age. Frozen Euploid Embryo Transfer (FEET) is routinely performed under standard hormone replacement therapy (HRT) and could be considered the best model for evaluating the impact of the endometrial preparation in clinical pregnancy rate and also in miscarriage rate.

Recently several authors have paid attention to serum progesterone (P) as a possible factor influencing Frozen Embryo Transfer (FET) outcomes. P plays an important role in endometrial gland formation, embryonic implantation and pregnancy maintenance. Labarta et al. (2) described in blastocyst FET performed under HRT that serum P <9.2 ng/mL measured on the transfer day is associated to significantly lower ongoing pregnancy rate (OR 0.297, 95% CI:0.113-0.779).

Recently the investigators have analyzed 244 FEET performed under HRT in a retrospective study (3). Preimplantation genetic testing for aneuploidies (PGT-A) was carried out as previously described (4). Embryos that reached the blastocyst stage were biopsied and frozen immediately afterwards using the vitrification method (5). Euploid embryos were transferred in a subsequent cycle under HRT. Serum P was analyzed the day previous to FEET. Patients with serum P <10.6 ng/mL had significantly higher miscarriage rate (26.6% vs 9.5%, p=0.007) and lower live birth rate (47.5% vs 62.3 %, p= 0.029) than those with serum P >10.6 ng/mL. The investigators also observed that patients with serum P >13.1 ng/mL had the lowest miscarriage rate (9.1%) and the highest live birth rate (65.6%). The worst outcomes were observed when serum P was <8.06 ng /mL (41% live birth rate and 32.4% miscarriage rate).

As miscarriage was higher among FEET cycles with serum P <10.6 ng/ml, the investigators hypothesize that altering the progesterone supplementation scheme could potentially reduce miscarriage rates and increase live birth rate. The purpose of this study is to modify the standard progesterone supplementation in FEET under HRT (vaginal micronized progesterone 200 mg every 8 hours) (6) according to serum P measured not only on the day prior to transfer but also on Beta subunit of Human Chorionic Gonadotropin (β-hCG) analysis day, and to probe if this intervention reduces miscarriage rate and increases pregnancy outcome.

Condition or Disease Intervention/Treatment Phase
  • Drug: Low Progesterone
  • Drug: Normal Progesterone
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
598 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effect of Intervention on Progesterone Levels Before Euploid Embryo Transfer in Pregnancy Outcomes
Actual Study Start Date :
Nov 15, 2018
Actual Primary Completion Date :
Feb 28, 2020
Actual Study Completion Date :
Feb 28, 2020

Arms and Interventions

Arm Intervention/Treatment
Other: Normal Progesterone group

Progesterone level >10.64 ng/mL on day 4 of progesterone supplementation

Drug: Normal Progesterone
Same Progesterone supplementation (vaginal micronized P 200mg/200mg/200mg) Warming and transfer on D5 Beta-hCG and P analysis is performed on the 14th day of P supplementation (D14). In case of positive Beta-hCG analysis: If P is >10.64 ng /mL: the same P supplementation is continued. If P is <10.64 ng /mL: an additional dosage of vaginal micronized P (200 mg) is added at night

Experimental: Low Progesterone group

Progesterone level <10.64 ng/mL on day 4 of progesterone supplementation

Drug: Low Progesterone
Additional daily dosage of subcutaneous progesterone (Psc) 25 mg/day at night since D4 (vaginal micronized P 200mg/200mg/200mg + Psc 25 mg/night) New Progesterone analysis on D5 before warming the embryo. Group 2a (Canceled Group, P on D5 <10.64 ng/mL): cancel PGT-FET. Scheduling a new procedure under different P supplementation. Group 2b (Restored Progesterone Group, P on D5 >10.64 ng/mL): continue HRT as previously described (vaginal micronized P 200mg/200mg/200mg + Psc 25 mg/night). Warming and transfer the same day (D5) Beta-hCG and P analysis is performed on the 14th day of P supplementation (D14). In case of positive Beta-hCG analysis: If P is >10.64 ng /mL: the same P supplementation is continued. If P is <10.64 ng /mL: an additional dosage of vaginal micronized P (200 mg) is added at night

Outcome Measures

Primary Outcome Measures

  1. Ongoing Pregnancy Rate (OPR) [12 weeks after transfer procedure]

    Ongoing Pregnancy Rate (OPR) beyond pregnancy week 12 in FEET according to serum P level and interventions on D4 and D5

  2. Miscarriage Rate (MR) [12 weeks after transfer procedure]

    Miscarriage Rate (MR) in FEET according to serum P level and interventions on D4 and D5.

  3. Concentration of serum P level [D4, D5 and D14 of P supplementation]

    P level

Secondary Outcome Measures

  1. Rate of cancellation due to lack of response in case of additional Psc dose on D4. [Day 5 of progesterone supplementation]

  2. Rate of rescued cycles in case of additional Psc dose [Day 5 of progesterone supplementation]

  3. Ongoing Pregnancy Rate and Live Birth Rate according to serum P level and interventions n D14 [On day 14 of progesterone supplementation]

  4. Live birth Rate (LBR) [40 weeks after transfer procedure]

    Live birth Rate (LBR) in FEET according to serum P level and interventions on D4 and D5 and D14.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • FEET of at least one single embryo

  • HRT

  • Endometrial thickness >= 6 mm measured day 4 of progesterone supplementation

Exclusion Criteria:
  • Patients with mosaic embryos.

  • Uterine abnormality.

  • Natural cycle protocol

Contacts and Locations

Locations

Site City State Country Postal Code
1 Departamento Ginecología, Obstetricia y Reproducción . Hospital Universitari Dexeus Barcelona Spain 08028

Sponsors and Collaborators

  • Institut Universitari Dexeus
  • Fundación Santiago Dexeus Font
  • Dexeus Clinic Woman

Investigators

  • Study Chair: Bueaventura Coroleu, PhD, Hospital Universitari Dexeus. Departamento de Ginecología, Obstetricia y Reproducción

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Buenaventura Coroleu, Head Reproductive Service, Institut Universitari Dexeus
ClinicalTrials.gov Identifier:
NCT03740568
Other Study ID Numbers:
  • FSD-PRG-2018-09
First Posted:
Nov 14, 2018
Last Update Posted:
Jul 29, 2020
Last Verified:
Jul 1, 2020
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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 29, 2020