TY - JOUR
T1 - Intracytoplasmic sperm injection (ICSI) versus conventional in vitro fertilisation (IVF) in couples with non-severe male infertility (NSMI-ICSI)
T2 - protocol for a multicentre randomised controlled trial
AU - Zheng, Danni
AU - Zeng, Lin
AU - Yang, Rui
AU - Lian, Ying
AU - Zhu, Yi-Min
AU - Liang, Xiaoyan
AU - Tang, Li
AU - Wang, Huichun
AU - Cao, Yunxia
AU - Hao, Guimin
AU - Liu, Jianqiao
AU - Zhao, Junli
AU - Wang, Rui
AU - Mol, Ben Willem
AU - Li, Rong
AU - Huang, He Feng
AU - Qiao, Jie
N1 - Funding
This study was supported by National Key Research and Development
Program of China (2016YFC1000201; 2018YFC1002104) and the National Science
Foundation of China (81730038). The study funders had no rule in the study design,
implementation, analysis, manuscript, preparation or decision to submit this article
for publication.
PY - 2019/9/30
Y1 - 2019/9/30
N2 - Introduction Intracytoplasmic sperm injection (ICSI), originally introduced as add-on to in vitro fertilisation (IVF) for couples with severe male infertility, is in current clinical practice also used in couples with mild male or even unexplained infertility. However, ICSI has involved unresolved concerns regarding the selection and damage to gametes and the health conditions of the offspring, and it is also labour intensive and therefore more expensive than conventional IVF. High-quality well-powered randomised clinical trials (RCTs) comparing ICSI and IVF are lacking. Methods and analysis We propose a multicentre, open-label RCT in 10 reproductive medical centres across China. We will study couples with non-severe male infertility (defined as a semen concentrate 5-15×10 6/mL or sperm with a progressive motility 10%-32%) scheduled for their first or second ICSI or IVF cycle, as low fertility rate after fertilisation are more frequent in this population, which could lead to controversy about ICSI or conventional IVF for fertilisation. On the day of oocyte retrieval, eligible participants are after informed consent be randomised to undergo either ICSI or conventional IVF in a 1:1 treatment ratio. Other standard assisted reproductive treatments are similar and parallel between two groups. Our primary outcome is ongoing pregnancy leading to live birth after the first cycle with embryo transfer. To demonstrate or refute a difference of 7% between ICSI and conventional IVF, we need to include 2346 women (1173 in each intervention arm). In addition, we will follow-up neonatal outcomes after delivery to identify the influence of ICSI on offspring. Ethics and dissemination Ethical approval was obtained from Peking University Third Hospital medical science research ethics committee. The findings will be disseminated to the public through conference presentations and peer-reviewed scientific journals.
AB - Introduction Intracytoplasmic sperm injection (ICSI), originally introduced as add-on to in vitro fertilisation (IVF) for couples with severe male infertility, is in current clinical practice also used in couples with mild male or even unexplained infertility. However, ICSI has involved unresolved concerns regarding the selection and damage to gametes and the health conditions of the offspring, and it is also labour intensive and therefore more expensive than conventional IVF. High-quality well-powered randomised clinical trials (RCTs) comparing ICSI and IVF are lacking. Methods and analysis We propose a multicentre, open-label RCT in 10 reproductive medical centres across China. We will study couples with non-severe male infertility (defined as a semen concentrate 5-15×10 6/mL or sperm with a progressive motility 10%-32%) scheduled for their first or second ICSI or IVF cycle, as low fertility rate after fertilisation are more frequent in this population, which could lead to controversy about ICSI or conventional IVF for fertilisation. On the day of oocyte retrieval, eligible participants are after informed consent be randomised to undergo either ICSI or conventional IVF in a 1:1 treatment ratio. Other standard assisted reproductive treatments are similar and parallel between two groups. Our primary outcome is ongoing pregnancy leading to live birth after the first cycle with embryo transfer. To demonstrate or refute a difference of 7% between ICSI and conventional IVF, we need to include 2346 women (1173 in each intervention arm). In addition, we will follow-up neonatal outcomes after delivery to identify the influence of ICSI on offspring. Ethics and dissemination Ethical approval was obtained from Peking University Third Hospital medical science research ethics committee. The findings will be disseminated to the public through conference presentations and peer-reviewed scientific journals.
KW - assisted reproductive technology
KW - in vitro fertilisation
KW - intracytoplasmic sperm injection
KW - non-severe male infertility
UR - http://www.scopus.com/inward/record.url?scp=85072848364&partnerID=8YFLogxK
U2 - 10.1136/bmjopen-2019-030366
DO - 10.1136/bmjopen-2019-030366
M3 - Article
C2 - 31575574
AN - SCOPUS:85072848364
VL - 9
JO - BMJ Open
JF - BMJ Open
SN - 2044-6055
IS - 9
M1 - e030366
ER -