A comparison of the effects of three different luteal phase support protocols on in vitro fertilization outcomes: a randomized clinical trial
- PMID: 20674911
- DOI: 10.1016/j.fertnstert.2010.06.057
A comparison of the effects of three different luteal phase support protocols on in vitro fertilization outcomes: a randomized clinical trial
Abstract
Objective: To evaluate the effects of three different luteal phase support protocols on pregnancy and implantation rates, as well as luteal phase hormone profile in intracytoplasmic sperm injection-ET cycles.
Design: A prospective, randomized study.
Setting: A tertiary teaching and research hospital.
Patient(s): Two hundred eighty-eight patients who were undergoing intracytoplasmic sperm injection with a long protocol of controlled ovarian hyperstimulation.
Intervention(s): Group 1 (E(2) + P) received daily P plus 4 mg of E(2), group 2 (hCG + P) received P plus 1,500 IU of hCG, and group 3 (P only) received daily vaginal P gel. Blood samples were drawn on the day of hCG administration, as well as 7 and 10 days after the hCG for the E(2) and P measurements.
Main outcome measure(s): The clinical pregnancy rate.
Result(s): No difference existed between the E(2) + P and hCG + P groups with respect to pregnancy rate, but it was significantly lower in the P-only group.The implantation rate was significantly lower in the P-only group than in the other groups.The highest miscarriage rate was in the P-only group (38%).
Conclusion(s): In assisted reproductive technology cycles including treatment with GnRH agonist, adding 4 mg of oral E(2) to P during the luteal phase significantly increased the pregnancy and implantation rates and decreased the miscarriage rate compared with the use of P only.
Copyright © 2011 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.
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