Efficacy and Safety of Gushen Antai Pill on Ongoing Pregnancy Rate in Women With Normal Ovarian Reserve Undergoing IVF-ET

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexFemale
Age21-42
SponsorShandong University of Traditional Chinese Medicine

About this trial

The purpose of this study is to investigate whether oral Gushen Antai pills supplementation for luteal phase support will improve ongoing pregnancy rate in women with normal ovarian reserve in fresh embryo transfer cycles.

Eligibility criteria

Qualifiers

Patients with normal ovarian function reserve (5 ≤ AFC ≤ 15, 1.2 ng/ml ≤ AMH ≤ 3.5 ng/ml).

Patients with regular menstrual cycle (21-35 days) and normal ovulation.

Initial IVF / ICSI treatment.

At least one embryo or blastocyst available for transfer.

Disqualifiers

Age ≥ 43 years old.

Body mass index (BMI) ≥ 28 Kg/m2.

"Freeze-all" strategy.

Those using the natural cycle or mild stimulation for IVF/ICSI treatment.

Trial design

Treatments tested in this trial

  • Gushen Antai Pill
  • Placebo pill

Treatment groups

800 Participants
are divided into 2 treatment groups