Actively Recruiting

Phase Not Applicable
Age: 0 - 43Years
All Genders
NCT06005311

Microfluidic Chip Method Versus Density-gradient Centrifugation Method in IVF

Led by Professor Ernest Hung-Yu Ng · Updated on 2024-12-06

1136

Participants Needed

1

Research Sites

265 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Infertile patients attending IVF treatment at the Centre of Assisted Reproduction and Embryology, Queen Mary Hospital and Kwong Wah Hospital will be recruited during ovarian stimulation for IVF. Subsequently, they will be randomly assigned on the day of oocyte retrieval by a laboratory staff into one of the following two groups: (1) the microfluidic chip group and (2) the density gradient group for sperm preparation and subsequent use in fertilization. Other IVF procedures will be the same as our usual practice. Both patients and clinicians were blinded from the group allocation i.e. a double blind study. The primary outcome is the cumulative live birth rate defined as the number of pregnancies leading to live birth within 6 months of randomisation.

CONDITIONS

Official Title

Microfluidic Chip Method Versus Density-gradient Centrifugation Method in IVF

Who Can Participate

Age: 0 - 43Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Infertile women aged under 43 years at the time of ovarian stimulation for IVF
Not Eligible

You will not qualify if you...

  • Women undergoing preimplantation genetic testing for monogenic diseases, structural chromosome rearrangements, or aneuploidy
  • Male factor infertility requiring surgical sperm retrieval such as microscopic epididymal sperm aspiration or testicular sperm extraction
  • Use of donor oocytes or donor sperm
  • Presence of submucosal fibroid or hydrosalpinx on pelvic scan that has not been surgically treated
  • Women previously recruited into this study
  • Women participating in other randomized trials

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Department of Obstetrics and Gynaecology

Hong Kong, Hong Kong, China

Actively Recruiting

Loading map...

Research Team

Y

YU WING TONG, MBBS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here