Hyaluronan-enriched Embryo Transfer Medium for Frozen-thawed Embryo Transfer
Study Details
Study Description
Brief Summary
This is a randomized-controlled trial evaluating the effect of the use of hyaluronan (HA)-enriched embryo transfer medium on the live birth rate in women undergoing frozen-thawed embryo transfer. For half of the women, hyaluronan-enriched medium will be used as embryo transfer medium. For the other half of women, a control will be used.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
Women being scheduled for FET will be assessed for eligibility. Eligible women will be recruited for the study and each woman will only be included in the study with one FET cycle. Informed written consent will be obtained. Their baseline characteristics will be collected.
Women with regular ovulatory cycles will undergo the standard procedures of blood taking to identify the day of luteinizing hormone (LH) surge. Women with irregular cycles will either receive clomiphene or letrozole followed by detection of the LH surge, or undergo hormone replacement therapy (HRT) cycle with oral oestradiol 6 mg daily for 14 days for endometrial priming followed by the addition of vaginal micronized progesterone 100 mg three times daily. HRT cycle may also be used for scheduling purposes.
Embryo transfer will be performed 3 or 4 days (for cleavage-stage embryos) or 6 or 7 days (for blastocysts) after the LH surge. For women in HRT cycles, FET will be scheduled on the 4th or 5th day (for cleavage-stage embryos) or the 7th or 8th day (for blastocysts) of starting vaginal progesterone. They will continue oral oestradiol and vaginal progesterone after FET up to 12 weeks of gestation.
Randomization:
One day before scheduled FET, recruited women will be randomized into one of the following two groups: (1) HA group and (2) control group according to a computer-generated randomization list prepared by a designated research nurse.
One the day of FET, frozen embryos or blastocysts will be thawed and incubated for at least 10 minutes in embryo transfer medium. For women allocated to the HA group, EmbryoGlue (Vitrolife) will be used as embryo transfer medium, while in the control group the usual medium used in the study center will used. The main difference between the two media is that EmbryoGlue contains a higher concentration of HA.
The rest of the embryo transfer procedure will be the same as the usual practice.
Blinding:
The patient and the physicians performing the FET and involved in her care will not know the group allocation. Only the embryologist will know the group allocation, but they will not be involved in the patient care, the FET procedure and subsequent assessment.
Follow-up and data collection:
A urine pregnancy test is performed 18 days after the LH surge or starting vaginal progesterone. If the pregnancy test is positive, transvaginal ultrasound will be performed 2 weeks later to locate the pregnancy and fetal viability. Subsequent management will be the same as other women with early pregnancy. They will be referred for antenatal care when the pregnancy is on-going at 8 weeks.
Follow-up:
Written consent regarding retrieval of pregnancy and delivery data from both public and private sectors will be sought from the patient at the time of study. The obstetric outcomes will be traced from the electric patient record system if the patients deliver in Hospital Authority hospitals. A pre-formatted letter with replying address available will be given to the patient at the end of the study period and is to be filled by the private obstetrician and returned to us after delivery. If no reply letter is received 2-3 months after the expected date of confinement of the patient, a letter including patient's authorization will be sent to the corresponding private obstetrician to retrieve the information of the pregnancy outcomes. The outcome of the pregnancy (delivery, miscarriage), number of babies born, birth weights and obstetrics complications will be recorded.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: HA group One the day of frozen-thawed embryo transfer, frozen embryos will be thawed and incubated for at least 10 minutes in embryo transfer medium. For women allocated to the HA group, EmbryoGlue (Vitrolife), a hyaluronan-enriched embryo transfer medium, will be used as embryo transfer medium. EmbryoGlue contains a higher concentration of hyaluronan than the control medium. |
Other: EmbryoGlue (Vitrolife)
A hyaluronan-enriched embryo transfer medium
|
| Active Comparator: Control group For women allocated to the control group, the usual transfer medium used in the study centers will be used and will serve as control. The main difference between the two media is that EmbryoGlue contains a higher concentration of HA. |
Other: Control medium
The usual embryo transfer medium used in the study centres.
|
Outcome Measures
Primary Outcome Measures
- Live-birth rate per embryo transfer procedure [1 year]
Secondary Outcome Measures
- pregnancy rate [4 weeks]
positive urine pregnancy test
- clinical pregnancy rate [4 weeks]
presence of intrauterine gestational sac on ultrasound
- implantation rate [8 weeks]
number of gestational sacs per embryo transferred
- on-going pregnancy rate [8 weeks]
viable pregnancy beyond gestation 8 weeks
- adverse events [12 weeks]
- obstetric complications [1 year]
Eligibility Criteria
Criteria
Inclusion Criteria:
- Women panning to replacing early cleavage embryos or blastocysts after thawing.
Exclusion Criteria:
-
Frozen early cleavage embryos thawed and cultured to blastocysts prior to transfer as requested by the patient
-
Preimplantation genetic diagnosis treatment
-
Use of donor oocytes or donor embryos
-
Endometrial thickness <8mm on the day of the luteinizing hormone surge or after two weeks of estrogen in hormonal replacement cycles
-
Hydrosalpinx shown on pelvic scanning and not surgically treated
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Kwong Wah Hospital | Hong Kong | Hong Kong | ||
| 2 | Queen Mary Hospital, University of Hong Kong | Hong Kong | Hong Kong |
Sponsors and Collaborators
- The University of Hong Kong
- Kwong Wah Hospital
Investigators
- Principal Investigator: Shuk Fei Sofie Yung, MBBS, The University of Hong Kong
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- UW 16-158