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Clinical Trials/NCT05017740
NCT05017740
Active, not recruiting
Not Applicable

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.

KK Women's and Children's Hospital1 site in 1 country47 target enrollmentMarch 15, 2022
ConditionsInfertilityIVF

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Infertility
Sponsor
KK Women's and Children's Hospital
Enrollment
47
Locations
1
Primary Endpoint
Clinical pregnancy rate
Status
Active, not recruiting
Last Updated
8 months ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
March 15, 2022
End Date
December 1, 2025
Last Updated
8 months ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Sponsor
KK Women's and Children's Hospital
Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

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

Miscarriage rate

Time Frame: 6 to 23+6 gestational weeks

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

Secondary Outcomes

  • Fertilisation rate(2-5 days after oocyte retrieval)
  • Live birth rate(After 24 completed weeks of gestation)

Study Sites (1)

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