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RCT on the Effect of Endometrial Injury on Ongoing Pregnancy Rate in Subfertile Women Undergoing IVF

Primary Purpose

Subfertility

Status
Completed
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Endometrial aspiration by pipelle
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 Endometrial injury, Pipelle, Implantation, Ongoing pregnancy rate, IVF

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Undergoing IVF for tubal, unexplained or male factor subfertility
  • Normal uterine cavity as shown on saline sonogram / hysteroscopy done at baseline

Exclusion Criteria:

  • Presence of hydrosalpinx
  • Presence of endometrial polyp or fibroid distorting uterine cavity
  • IVF cycles carried out for preimplantation genetic diagnosis
  • Use of donor gametes

Sites / Locations

  • University of Hong Kong

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Endometrial Aspirate (EA) group

Control group

Arm Description

Endometrial aspirate by pipelle

No intervention prior to scheduled IVF

Outcomes

Primary Outcome Measures

Ongoing pregnancy rate
Ongoing pregnancy rate per fresh embryo transfer

Secondary Outcome Measures

implantation rate
number of gestation sac on pelvic scan per number of embryo transferred

Full Information

First Posted
October 31, 2013
Last Updated
December 2, 2014
Sponsor
The University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT01977976
Brief Title
RCT on the Effect of Endometrial Injury on Ongoing Pregnancy Rate in Subfertile Women Undergoing IVF
Official Title
A Randomized Controlled Trial on the Effect of Endometrial Injury on Improving Ongoing Pregnancy Rate in Subfertile Women Undergoing in Vitro Fertilization Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
April 2014 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Implantation failure remains one of the major factors limiting success in IVF treatment. It was postulated that the local injury to endometrium induces secretions of cytokines and growth factors such as leukemia inhibitory factor, interleukin-11, and heparin-binding EGF-like growth factor which enhance decidualisation and facilitate implantation. It may also up-regulate the gene expressions related to endometrial receptivity and optimize the endometrial development. In stimulated cycles, local injury to the proliferative endometrium has been postulated to delay endometrial development thereby inducing synchronicity between endometrium and embryo stage and facilitate implantation (Zhou et al, 2008; Almog et al, 2010; Gnainsky et al, 2010) The aim of the study is to determine whether endometrial injury by endometrial biopsy in mid-secretory phase of the preceding cycle would improve the on-going pregnancy rate in subfertile women undergoing IVF treatment.
Detailed Description
Consecutive women attending subfertility clinic at Queen Mary Hospital, University of Hong Kong who are scheduled for IVF 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. Patients will be stratified according to the first or repeated cycle. For patients in the study group, in the cycle immediately preceding the scheduled IVF treatment, LH surge will be determined by daily serum LH level starting from 18 days before the next expected period. LH surge is defined as an elevation of LH to 2 times the level of the average of the previous 3 days and the absolute level of the LH should be more than or equal to 20 IU/L. Women randomized into the study group will have endometrial biopsy performed by pipelle 7 days after the LH surge (LH+7) and they will be instructed to use non-hormonal means of contraception during that cycle. All patients will then proceed to IVF treatment in the next cycle as scheduled. They will receive standard ovarian stimulation according to the departmental protocol and have a maximum of two embryos replaced 2 days after the oocyte retrieval. On-going pregnancy rates between the two groups will be compared.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Subfertility
Keywords
Endometrial injury, Pipelle, Implantation, Ongoing pregnancy rate, IVF

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Endometrial Aspirate (EA) group
Arm Type
Experimental
Arm Description
Endometrial aspirate by pipelle
Arm Title
Control group
Arm Type
No Intervention
Arm Description
No intervention prior to scheduled IVF
Intervention Type
Procedure
Intervention Name(s)
Endometrial aspiration by pipelle
Intervention Description
Endometrial aspiration by pipelle is to be performed on LH+7 in the cycle preceding scheduled IVF treatment
Primary Outcome Measure Information:
Title
Ongoing pregnancy rate
Description
Ongoing pregnancy rate per fresh embryo transfer
Time Frame
10-12 weeks gestation
Secondary Outcome Measure Information:
Title
implantation rate
Description
number of gestation sac on pelvic scan per number of embryo transferred
Time Frame
4 weeks after embryo transfer
Other Pre-specified Outcome Measures:
Title
Clinical pregnancy rate
Description
Presence of at least one fetal heart pulsation per fresh embryo transfer 4 weeks after transfer
Time Frame
4 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
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Undergoing IVF for tubal, unexplained or male factor subfertility Normal uterine cavity as shown on saline sonogram / hysteroscopy done at baseline Exclusion Criteria: Presence of hydrosalpinx Presence of endometrial polyp or fibroid distorting uterine cavity IVF cycles carried out for preimplantation genetic diagnosis Use of donor gametes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tracy Yeung, MRCOG
Organizational Affiliation
The University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Hong Kong
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

Citations:
PubMed Identifier
25205759
Citation
Yeung TW, Chai J, Li RH, Lee VC, Ho PC, Ng EH. The effect of endometrial injury on ongoing pregnancy rate in unselected subfertile women undergoing in vitro fertilization: a randomized controlled trial. Hum Reprod. 2014 Nov;29(11):2474-81. doi: 10.1093/humrep/deu213. Epub 2014 Sep 8.
Results Reference
derived

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RCT on the Effect of Endometrial Injury on Ongoing Pregnancy Rate in Subfertile Women Undergoing IVF

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