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NCT Number: NCT05017740

PICSI RCT in Couples With a Previous Poor Fertilisation Cycle in IVF

Poor fertilisation plays a significant role in poor artificial reproductive technique outcomes. Male factor infertility accounts for a large portion of such cases. Several modalities have been proposed as a solution, including physiological intra-cytoplasmic sperm injection (PICSI). PICSI is a technique used to select the sperm to use in intra-cytoplasmic sperm injection (ICSI) treatment. It involves placing sperm with hyaluronic acid, a natural compound found in the body. PICSI identifies sperm that can bind to hyaluronic acid and these sperms are selected for use in treatment.

Some studies have suggested that PISCI may be advantageous to reduce miscarriage. However, the evidence is not strong and it remains unknown if PICSI is effective in a selected group of couples with a history of poor fertilisation. Based on previous medical records, we observed a higher clinical pregnancy rate (CPR) and a trend towards lower miscarriage rates with PICSI. To verify the findings and address the clinical gap, we propose a randomised controlled trial (RCT) with 234 couples (117 in each group) to evaluate the effectiveness of PICSI comparing with ICSI for improving CPR and reducing miscarriage rate in couples with a fertilisation rate of <50% in their first cycle of ICSI.

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Key information

Age range

21 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

KK Women's and Children's Hospital

Singapore, 229899

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Couples with <50% fertilisation in their first ICSI cycle, and scheduled for their second ICSI/PICSI cycle

Exclusion criteria

  • Women with diminished ovarian reserves (AMH <1.2ng/ml) or severe endometriosis (rAFS Stage III or IV)
  • Male partner with severe oligoasthenoteratozoospermia (Density < 5 million, Total motility < 40) or those require surgically retrieved sperm
  • Couples using donor gametes
  • Couples using frozen gametes
  • Couples undergoing split IVF-ICSI cycles
  • Couples where a freeze all approach has been done, either clinically indicated or secondary to patient choice

Treatment and study plan

ICSI

Procedure

In ICSI, the sperm is chosen based on motility and gross morphology to be inseminated directly into the cytoplasm of the oocyte.

PICSI

Procedure

In PICSI, the sperm is selected via hyaluronic binding before insemination into the cytoplasm of the oocyte.

Primary outcomes

  1. Clinical pregnancy rate

    Time frame: 6-9 weeks after fresh embryo transfer

    The presence of fetal heartbeat or gestational sac at 6-9 weeks after fresh embryo transfer

  2. Miscarriage rate

    Time frame: 6 to 23+6 gestational weeks

    Pregnancy loss before 23+6 completed weeks after confirmation of clinical pregnancy

Secondary outcomes

  1. Fertilisation rate

    Time frame: 2-5 days after oocyte retrieval

    Successful embryo transfer

  2. Live birth rate

    Time frame: After 24 completed weeks of gestation

    Live birth after 24 completed weeks of gestation

Sponsors and collaborators

Lead sponsor

KK Women's and Children's Hospital

Other Gov

Registry information

Official study title

A Randomised Clinical Trial in the Use of Physiological Intra-cytoplasmic Spermatozoa Injection (PICSI) in Couples With a Previous Poor Fertilisation Cycle in In-vitro Fertilisation.

Important dates

Study start
2022
Primary completion
2025
Study completion
2025
First posted
Aug 24, 2021
Registry last updated
Aug 27, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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