search
Back to results

A RCT on the Effect of Endometrial Injury on Improving Ongoing Pregnancy Rate in Subfertile Women Undergoing FET Cycles

Primary Purpose

Subfertility

Status
Terminated
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Endometrial biopsy
control procedure
Pipelle catheter (Pipelle de Cornier, Laboratoire C.C.D., France)
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Subfertility focused on measuring Frozen thawed embryo transfer, Endometrial injury, Ongoing pregnancy rates

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Undergoing FET treatment cycles
  • Normal uterine cavity as shown on transvaginal scanning or saline sonogram done at baseline
  • endometrial thickness >=8mm during the stimulated IVF cycle and FET cycle

Exclusion Criteria:

  • Pregnancy in previous IVF or FET cycles
  • Presence of hydrosalpinx not surgically corrected prior to FET
  • Presence of endometrial polyp or fibroid distorting uterine cavity
  • IVF cycles carried out for preimplantation genetic diagnosis
  • Arrange for blastocyst transfer
  • Use of donor oocytes

Sites / Locations

  • Queen Mary Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

EA

Control

Arm Description

in the cycle immediately preceding the scheduled FET treatment, an endometrial biopsy would be arranged on day 21-23 of the menstrual cycles and they will be instructed to use non-hormonal means of contraception during that cycle.

The procedure was performed in a standard approach using a Pipelle catheter (Pipelle de Cornier, Laboratoire C.C.D., France). The pipelle catheter was introduced through the cervix but not into the uterine cavity, only entering the endocervical canal as control.

Outcomes

Primary Outcome Measures

Ongoing pregnancy rate
Pregnancy at 10-12 weeks

Secondary Outcome Measures

Implantation rate
Implantation rate = number of gestation sacs on ultrasound (USG) / number of embryos transferred
Clinical pregnancy rate
Clinical pregnancy rate is the presence of gestation sac on USG scan.

Full Information

First Posted
July 20, 2014
Last Updated
December 10, 2015
Sponsor
The University of Hong Kong
search

1. Study Identification

Unique Protocol Identification Number
NCT02197832
Brief Title
A RCT on the Effect of Endometrial Injury on Improving Ongoing Pregnancy Rate in Subfertile Women Undergoing FET Cycles
Official Title
A Randomized Controlled Trial on the Effect of Endometrial Injury on Improving Ongoing Pregnancy Rate in Subfertile Women Undergoing Frozen-thawed Embryo Transfer Treatment Cycles
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Terminated
Why Stopped
Difficulty in recruiting participants.
Study Start Date
September 2012 (undefined)
Primary Completion Date
March 2015 (Actual)
Study Completion Date
March 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Hong Kong

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a randomised controlled trial on the effect of endometrial injury in the cycle preceding the frozen-thawed embryo transfer (FET) cycles. The study hypothesis is that endometrial injury will increase the ongoing pregnancy rate in FET cycles.
Detailed Description
Consecutive women attending subfertility clinic at Queen Mary Hospital, University of Hong Kong who are scheduled for FET treatment will be recruited. Women who have normal uterine cavity will be randomized into study and control groups in 1 to 1 ratio according to a computer-generated randomization list. For patients in the study group, in the cycle immediately preceding the scheduled FET treatment, an endometrial biopsy would be arranged on day 21-23 of the menstrual cycles and they will be instructed to use non-hormonal means of contraception during that cycle. For patient in the control group, a similar procedure would be performed on the same timing during the preceding cycles without entering the uterine cavity, ie endometrial biopsy catheter entering the endocervical canal without entering the endometrial cavity. All patients will then proceed to FET treatment in the next cycle as scheduled. The FET would be carried out as per our protocol. In short, patients attend the clinic daily from 18 days before the next expected period for the determination of serum E2 and luteinising hormone (LH) concentrations until the LH surge, which was defined as the day on which the LH level was above 20 IU/L and doubled the average of the LH levels over the past three days. For patients with irregular menstrual cycles or no ovulation demonstrated during natural cycle monitoring, clomiphene citrate (CC, Clomid, Merrell, Staines, U.K.) 50-100 mg will be given daily for five days from Days 3-7. The cycle will be monitored by blood tests from day 10 of the cycle as above. FET was performed on the third day after the LH surge. Up to two frozen-thawed embryo(s) can be transferred. No luteal phase support is used. On-going pregnancy rates, defined as viable fetuses beyond 10-12 gestational weeks, between the two groups will be compared. We should measure endometrial thickness on LH+1 in natural and clomid-induced cycles.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Subfertility
Keywords
Frozen thawed embryo transfer, Endometrial injury, Ongoing pregnancy rates

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
EA
Arm Type
Experimental
Arm Description
in the cycle immediately preceding the scheduled FET treatment, an endometrial biopsy would be arranged on day 21-23 of the menstrual cycles and they will be instructed to use non-hormonal means of contraception during that cycle.
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
The procedure was performed in a standard approach using a Pipelle catheter (Pipelle de Cornier, Laboratoire C.C.D., France). The pipelle catheter was introduced through the cervix but not into the uterine cavity, only entering the endocervical canal as control.
Intervention Type
Procedure
Intervention Name(s)
Endometrial biopsy
Intervention Description
The procedure was performed in a standard approach using a Pipelle catheter (Pipelle de Cornier, Laboratoire C.C.D., France). The pipelle catheter was introduced through the cervix up to the uterine fundus. The piston was drawn back to the end of the sheath to create a negative pressure. The sheath was rotated and moved back and forth between the fundus and internal os for at least 3-4 times before it was gently withdrawn.
Intervention Type
Procedure
Intervention Name(s)
control procedure
Intervention Description
Using pipelle catheter without entering the uterine cavity.
Intervention Type
Device
Intervention Name(s)
Pipelle catheter (Pipelle de Cornier, Laboratoire C.C.D., France)
Primary Outcome Measure Information:
Title
Ongoing pregnancy rate
Description
Pregnancy at 10-12 weeks
Time Frame
pregnancy at 10-12 weeks
Secondary Outcome Measure Information:
Title
Implantation rate
Description
Implantation rate = number of gestation sacs on ultrasound (USG) / number of embryos transferred
Time Frame
4-6 weeks after embryo transfer
Title
Clinical pregnancy rate
Description
Clinical pregnancy rate is the presence of gestation sac on USG scan.
Time Frame
6 weeks after embryo transfer

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Undergoing FET treatment cycles Normal uterine cavity as shown on transvaginal scanning or saline sonogram done at baseline endometrial thickness >=8mm during the stimulated IVF cycle and FET cycle Exclusion Criteria: Pregnancy in previous IVF or FET cycles Presence of hydrosalpinx not surgically corrected prior to FET Presence of endometrial polyp or fibroid distorting uterine cavity IVF cycles carried out for preimplantation genetic diagnosis Arrange for blastocyst transfer Use of donor oocytes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vivian CY Lee, MBBS
Organizational Affiliation
Queen Mary Hospital / University of Hong Kong.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Queen Mary Hospital
City
Hong Kong
ZIP/Postal Code
852
Country
Hong Kong

12. IPD Sharing Statement

Learn more about this trial

A RCT on the Effect of Endometrial Injury on Improving Ongoing Pregnancy Rate in Subfertile Women Undergoing FET Cycles

We'll reach out to this number within 24 hrs