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Natural Cycle or Stimulated Cycle Versus Hormone Replaced Cycle for Pre-eclampsia Rate

W

Women's Hospital School Of Medicine Zhejiang University

Status

Unknown

Conditions

Pre-Eclampsia

Treatments

Other: hormone replaced cycle for endometrium preparation
Other: natural cycle for endometrium preparation

Study type

Interventional

Funder types

Other

Identifiers

NCT04310683
PREECLAMPSIA

Details and patient eligibility

About

Recent sutdies indicate that the existence of corpus lutein in the ovary is a key point to prevent preeclampsia, and patients undergoing FET with hormone replaced cycle have no corpus lutein and the absence of corpus lutein significantly increases the risk of preeclampsia in these patients. We aim to conduct a single center randomized trial study to compare the preeclampsia rate between the natural cycle and the hormone replaced cycle in patients undergoing FET.

Enrollment

840 estimated patients

Sex

Female

Ages

18 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. 18 to 42 years old women;
  2. normal ovulation;
  3. Scheduled to undergo frozen-thawed embryo transfer.
  4. Agreeing with the informed consent.

Exclusion criteria

  1. Those who experienced embryo transfer cycle failure for at least three times;
  2. One or both of the ovaries removed;
  3. Hypertention disease before embryo transfer;
  4. No available embryo for transfer
  5. Oocyte or sperm donated cycles

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

840 participants in 2 patient groups

natural cycle for endometrium preparation
Other group
Description:
patients will have ovulation before embryo transfer
Treatment:
Other: natural cycle for endometrium preparation
hormone replaced cycle for endometrium preparation
Experimental group
Description:
patients will do not have ovulation before embryo transfer
Treatment:
Other: hormone replaced cycle for endometrium preparation

Trial contacts and locations

0

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Central trial contact

Dan Zhang, M.D. Ph.D.; Kai-Lun Hu, M.D.

Data sourced from clinicaltrials.gov

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