Overview

Luteal Support in Frozen-Thawed Embryo Transfer Cycles

Status:
Not yet recruiting
Trial end date:
2021-11-01
Target enrollment:
0
Participant gender:
Female
Summary
This study evaluates the clinical efficacy of 3 different luteal phase support in patients undergoing frozen-thawed embryo transfer cycles. Endometrium preparation will be hormone replacement in all cycles. Starting from day 11, group 1 will receive 100 mg micronized progesterone parenteral daily injections, group 2 will receive 90 mg bioadhesive gel vaginal twice daily and group 3 will receive 40 mg oral dydrogesterone daily tablets.
Phase:
Phase 4
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Centrum Clinic IVF Center
Treatments:
Dydrogesterone
Progesterone
Criteria
Inclusion Criteria:

- woman aged 20-40 years

- Having available blastocyst(s) cryopreserved by vitrification method.

Exclusion Criteria:

- requirement for fresh embryo(s);

- presence of any clinically relevant systemic disease contraindicated for assisted
reproduction or pregnancy

- history of more than three failed cycles of IVF

- history of recurrent abortions

- allergy history for relevant drugs

- body mass index of <18 or >38 kg/m2 at screening

- current breastfeeding or pregnancy

- refusal or inability to comply with the requirements of the protocol for any reason,
including scheduled clinic visits and laboratory tests

- trophectoderm or blastomere biopsy of the blastocyst(s) to be transferred