Prospective Randomized Trial Comparing Embryo Transfers of Cases with and without Catheter Rotation during Its Withdrawal

Gynecol Obstet Invest. 2018;83(4):397-403. doi: 10.1159/000489493. Epub 2018 May 14.

Abstract

Objective: To compare embryo transfer (ET) technique based on catheter rotation during its withdrawal in cases with unexplained infertility in a prospective, randomized trial (NCT03097042).

Methods: Two hundred intracytoplasmic sperm injection (ICSI) patients undergoing ET with cleaving or blastocyst-stage fresh embryos were randomized into 2 groups: cases with (n = 100), and without (n = 100) catheter rotation during its withdrawal. Groups were matched for age and some clinical parameters. A soft catheter was used to transfer a single embryo with catheter rotation during its withdrawal in the study group and without rotation in the control. The use of a stiff catheter or tenaculum was not needed in any case. Groups were compared in terms of cycle characteristics and clinical pregnancy rates.

Results: Pregnancy rate was significantly higher in the study group (41 vs. 26%, p = 0.04). Clinical pregnancy rate was also significantly higher in the study group (39 vs. 25%, OR 1.9 [1.1-3.5], p = 0.05). On the other hand, the ongoing pregnancy rate was similar between the 2 groups (33 vs. 23%, p = 0.2).

Conclusion: Catheter rotation during its withdrawal may be associated with increased pregnancy and clinical pregnancy rates; however, the difference in ongoing pregnancy rates did not reach statistical significance.

Keywords: Assisted reproductive technique outcome; Assisted reproductive technology; Ultrasound-guided embryo transfer.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Catheters*
  • Device Removal / methods*
  • Embryo Transfer / instrumentation*
  • Embryo Transfer / methods
  • Female
  • Humans
  • Infertility / therapy*
  • Pregnancy
  • Pregnancy Rate
  • Prospective Studies
  • Rotation*
  • Sperm Injections, Intracytoplasmic / methods
  • Treatment Outcome

Associated data

  • ClinicalTrials.gov/NCT03097042