Effects of Recombinant LH in Patients With Repeated Implantation Failure (late-rLH)
Primary Purpose
Female Infertility, Female Subfertility
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
rFSH + r-LH in combination
rFSH alone
Sponsored by
About this trial
This is an interventional treatment trial for Female Infertility
Eligibility Criteria
Inclusion Criteria:
- Only patients with repeated implantation failure in at least two previous IVF cycles were included.
Exclusion Criteria:
- Patients were excluded from the study if they had any clinically significant systemic disease, polycystic ovarian syndrome (PCOS), a previous history of severe ovarian hyperstimulation syndrome (OHSS), abnormal gynaecological bleeding of unknown origin, a previous history of intolerance to any of the agents used in the study.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
rFSH + r-LH in combination
rFSH alone
Arm Description
treatment group
control group
Outcomes
Primary Outcome Measures
Number of ovocites retrived
Possible beneficial effects of rLH in the late phase of stimulation in patient with repeated implantation failure
Secondary Outcome Measures
Full Information
NCT ID
NCT03204253
First Posted
December 9, 2016
Last Updated
June 28, 2017
Sponsor
University of Roma La Sapienza
1. Study Identification
Unique Protocol Identification Number
NCT03204253
Brief Title
Effects of Recombinant LH in Patients With Repeated Implantation Failure
Acronym
late-rLH
Official Title
Effects of Recombinant LH in Late Phase of Ovarian Stimulation in Patients With Repeated Implantation Failure, Clinical Results
Study Type
Interventional
2. Study Status
Record Verification Date
June 2017
Overall Recruitment Status
Completed
Study Start Date
January 2016 (undefined)
Primary Completion Date
September 2016 (Actual)
Study Completion Date
September 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Roma La Sapienza
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Pregnancy rates fall dramatically in women after 35 years undergoing to IVF or ICSI. While ovarian aging obviously plays the major role in this phenomenon, over suppression of endogenous LH concentrations with GnRH agonists or antagonists-an integral part of standard IVF/ ICSI protocols-may also play a pivotal role.
Assisted reproduction technology protocols using GnRH agonists have been considered as the standard protocol during the last two decades, but the use of GnRH antagonists offers the opportunity to control the endogenous LH surge in a rapid and more convenient way.
LH plays a key role in the intermediate-late phases of folliculogenesis. The presence of receptors for LH in cumulus granulosa cells and its correlation with oocyte maturation has been demonstrated. Although ovarian stimulation is efficiently achieved in most cases by the administration of exogenous FSH alone, specific subgroups of women may benefit from LH activity supplementation during ovarian stimulation. Some authors have found improved outcome with LH activity supplementation in advanced reproductive age women.
LH has a number of roles in follicular development, induction of ovulation, completion of meiosis I, early luteinization and the production of progesterone.
The efficacy of recombinant human follicle-stimulating hormone (r-hFSH) for ovarian stimulation is well established however, the role of supplementary recombinant human luteinizing hormone (r-hLH) is less clear.
Aim of the present study is to evaluate If adding rLH in the late phase of stimulation can benefit in some patient awith repeated implantation failure.
Detailed Description
Study Design, Size and Duration
The study was conducted at the - Bio fertility IVF Center, Rome, Italy, on infertile couples due to male factor undergoing ICSI treatment.
The study was reviewed and approved by the institutional review board at the - Biofertilty IVF Center.
All patients undergoing ICSI and participating in the study gave informed consent.
Patients included in the study had regular spontaneous menstrual cycles (26-39 days) and were aged < 42 years.
All patients had acceptable follicular phase serum concentrations of FSH (≤10IU/L), LH (<10IU/L) and oestradiol (<60pg/ml), body mass index (BMI) ≤ 30 kg/m2, presence of both ovaries and normal uterine cavity.
Only patients with repeated implantation failure in at least two previous IVF cycles were included.
Patients were excluded from the study if they had any clinically significant systemic disease, polycystic ovarian syndrome (PCOS), a previous history of severe ovarian hyperstimulation syndrome (OHSS), abnormal gynaecological bleeding of unknown origin, a previous history of intolerance to any of the agents used in the study.
This was a prospective, randomized study.
All patient sighed a detailed informed consent.
The study is in accordance to the GCP guidelines
They were randomly divided into two groups (A and B).
All patients were stimulated in GnRH antagonist flexible protocol cycles using rFSH started on day 2 of a spontaneous or induced cycle. HCG (10000 iu ) was administered by I.M route when at least 2 folliclesreached 18 mm in diameter.
Group A included 29 women stimulated with rFSH supplemented by rLH in the late follicular phase started at the same time of starting the antagonist administration.
Those patients received 75 iu of rLH (Luveris serono) daily and 150 iu about 12 hours before triggering ovulation with HCG while Group B included 32 women who were stimulated with recombinant FSH (gonal F serono) only. The oocytes were decumulated and assessed for the maturation two hours after pick up which was done 36 hours after hcg injection. Mature oocyte should have an intact first polar body and homogeneously fine granular and light-colored ooplasm
The rate of metaphase II oocytes was calculated and the MII oocytes were assessed for cytoplasmic morphology and maturity. MII oocytes with a light color and fine homogeneous granulate ooplasm were considered oocytes normal morphology and classified as oocytes that have completed their cytoplasmic maturation.
Embryo transfer was done after 2 days of icsi. Pregnancy test was done after 12 days and clinical pregnancy and number of gestional sacs were assured after 2 weeks of positive pregnancy test with presence of featal heart beats. The mean, SD, T-test and Chi square test were used for statistic calculations of the results.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Female Infertility, Female Subfertility
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
rFSH + r-LH in combination
Arm Type
Experimental
Arm Description
treatment group
Arm Title
rFSH alone
Arm Type
Active Comparator
Arm Description
control group
Intervention Type
Drug
Intervention Name(s)
rFSH + r-LH in combination
Intervention Description
29 women stimulated with rFSH supplemented by rLH in the late follicular phase started at the same time of starting the antagonist administration.
Intervention Type
Drug
Intervention Name(s)
rFSH alone
Intervention Description
32 women who were stimulated with recombinant FSH alone
Primary Outcome Measure Information:
Title
Number of ovocites retrived
Description
Possible beneficial effects of rLH in the late phase of stimulation in patient with repeated implantation failure
Time Frame
1 cicle of stimulation of 14 days
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
42 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Only patients with repeated implantation failure in at least two previous IVF cycles were included.
Exclusion Criteria:
Patients were excluded from the study if they had any clinically significant systemic disease, polycystic ovarian syndrome (PCOS), a previous history of severe ovarian hyperstimulation syndrome (OHSS), abnormal gynaecological bleeding of unknown origin, a previous history of intolerance to any of the agents used in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Davide Francomano
Organizational Affiliation
University of Roma La Sapienza
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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Effects of Recombinant LH in Patients With Repeated Implantation Failure
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