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IVF Treatment in Women With Immature Oocytes in Previous Cycle

Primary Purpose

Infertility

Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
GnRH agonist 0.2 mg + hCG 250 mcg
high dose hCG 500 mcg
Sponsored by
Sheba Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring double triggering, Oocyte maturation, GNRH Agonist, hCG, IVF treatment, immature oocytes

Eligibility Criteria

18 Years - 42 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients with low proportion of mature-MII oocytes oocytes (75%) per number oocytes retrieved at the prior IVF cycle
  • Age between 18-42

Exclusion Criteria:

  • Women with high ovarian response:anti-mullerian hormone ( AMH) >5, antral follicle count ( AFC) >15
  • more than 20 oocytes retrieved at the prior cycle.

Sites / Locations

  • Sheba Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

High dose hCG

Double trigger

Arm Description

The hCG group- will be triggered for final follicular maturation with high dose hCG (500 mcg)-38 hours prior to oocyte aspiration

Double trigger Group- will receive GnRH agonist (Decapeptyl 0.2mg) 40 hours prior to oocyte aspiration and hCG (250mcg) 34 hours prior to the oocyte aspiration

Outcomes

Primary Outcome Measures

Number MII oocytes per number of oocytes retrieved
Rate of mature oocytes from total oocytes retrieved

Secondary Outcome Measures

Total oocytes
Pregnancy rate
Number of top quality embryos

Full Information

First Posted
February 10, 2015
Last Updated
June 23, 2022
Sponsor
Sheba Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02368964
Brief Title
IVF Treatment in Women With Immature Oocytes in Previous Cycle
Official Title
Treatment for Final Follicular Maturation Induction in Patients With Previous High Ratio of Immature Oocytes
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
February 1, 2015 (Actual)
Primary Completion Date
June 1, 2020 (Actual)
Study Completion Date
June 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sheba Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In standard IVF stimulation cycle,human chorionic gonadotropin (hCG) is usually used at the end of controlled ovarian hyperstimulation (COH) as a surrogate to only the luteinizing hormone (LH) surge. Yet, the last dose of follicle stimulating hormone (FSH) is usually given between 12-24 hours before the hCG triggering dose.One protocol used at the investigators unit, after a cycle with low proportion of mature oocytes per number oocytes retrieved, is triggering with high dose hCG (500 mcg)-38 hours prior to oocyte aspiration. Lately, new researches showed that dual triggering of final oocyte maturation with a combination of GnRH- agonist and hCG, could improve the live-birth rate of normal responders undergoing the GnRH-antagonist COH protocol Another treatment option is high dose hCG. Only few case reports have described the use of high dose hCG after aspiration of non mature oocytes at a previous cycle. At the investigators IVF unit, patients with previous history of high percentage of immature oocytes retrieved, are triggered at the following cycle, either with double trigger or with high dose of hCG decided by the physician consulting the patient. It is still not known with which way of triggering more mature oocytes is retrieved. The aim of this study is to perform a prospective randomized controlled study in patients with low proportion of mature-MII oocytes oocytes (<75%) per number oocytes retrieved, despite normal response to controlled ovarian hyperstimulation ( COH ) comparing cycles triggered with high dose hCG to those triggered with hCG+GnRH agonist.
Detailed Description
Patients will be prospectively randomized into two groups. The randomization will be organized through the computer. The hCG group- will be triggered for final follicular maturation with high dose hCG (500 mcg)-38 hours prior to oocyte aspiration, and the Double trigger Group- will receive gonadotropin-releasing hormone (GnRH) agonist (Decapeptyl 0.2mg) 40 hours prior to oocyte aspiration and hCG (250mcg) 34 hours prior to the oocyte aspiration. All patients will be supplemented with the same progesterone preparation( Crinone gel 8% once a day) for luteal support. Women that suffer from vaginal spotting or vaginal bleeding during the luteal phase will receive supplementation of Geston 50MG intramuscular once every 2 days. At the day of oocyte aspiration, blood will be drawn for serum LH, FSH, estrogen (E2) and progesterone. Moreover, clear follicular fluid will be collected and tested for LH, FSH, E2 and progesterone levels.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
double triggering, Oocyte maturation, GNRH Agonist, hCG, IVF treatment, immature oocytes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High dose hCG
Arm Type
Experimental
Arm Description
The hCG group- will be triggered for final follicular maturation with high dose hCG (500 mcg)-38 hours prior to oocyte aspiration
Arm Title
Double trigger
Arm Type
Experimental
Arm Description
Double trigger Group- will receive GnRH agonist (Decapeptyl 0.2mg) 40 hours prior to oocyte aspiration and hCG (250mcg) 34 hours prior to the oocyte aspiration
Intervention Type
Drug
Intervention Name(s)
GnRH agonist 0.2 mg + hCG 250 mcg
Other Intervention Name(s)
GnRH agonist - Decapeptyl , hCG - Ovitrelle
Intervention Description
Treatment for triggering
Intervention Type
Drug
Intervention Name(s)
high dose hCG 500 mcg
Other Intervention Name(s)
Ovitrelle
Intervention Description
Treatment for triggering
Primary Outcome Measure Information:
Title
Number MII oocytes per number of oocytes retrieved
Description
Rate of mature oocytes from total oocytes retrieved
Time Frame
day of retrieving the oocytes
Secondary Outcome Measure Information:
Title
Total oocytes
Time Frame
day of retrieving the oocytes
Title
Pregnancy rate
Time Frame
Two weeks from induction of ovulation
Title
Number of top quality embryos
Time Frame
day of retrieving the oocytes

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
42 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients with low proportion of mature-MII oocytes oocytes (75%) per number oocytes retrieved at the prior IVF cycle Age between 18-42 Exclusion Criteria: Women with high ovarian response:anti-mullerian hormone ( AMH) >5, antral follicle count ( AFC) >15 more than 20 oocytes retrieved at the prior cycle.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aya Mohr Sasson, M.D
Organizational Affiliation
Sheba Medical Center - IVF Unit
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sheba Medical Center
City
Ramat Gan
Country
Israel

12. IPD Sharing Statement

Citations:
PubMed Identifier
21315341
Citation
Lamb JD, Shen S, McCulloch C, Jalalian L, Cedars MI, Rosen MP. Follicle-stimulating hormone administered at the time of human chorionic gonadotropin trigger improves oocyte developmental competence in in vitro fertilization cycles: a randomized, double-blind, placebo-controlled trial. Fertil Steril. 2011 Apr;95(5):1655-60. doi: 10.1016/j.fertnstert.2011.01.019.
Results Reference
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PubMed Identifier
23993928
Citation
Lin MH, Wu FS, Lee RK, Li SH, Lin SY, Hwu YM. Dual trigger with combination of gonadotropin-releasing hormone agonist and human chorionic gonadotropin significantly improves the live-birth rate for normal responders in GnRH-antagonist cycles. Fertil Steril. 2013 Nov;100(5):1296-302. doi: 10.1016/j.fertnstert.2013.07.1976. Epub 2013 Aug 28.
Results Reference
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PubMed Identifier
25385007
Citation
Zilberberg E, Haas J, Dar S, Kedem A, Machtinger R, Orvieto R. Co-administration of GnRH-agonist and hCG, for final oocyte maturation (double trigger), in patients with low proportion of mature oocytes. Gynecol Endocrinol. 2015 Feb;31(2):145-7. doi: 10.3109/09513590.2014.978850. Epub 2014 Nov 11.
Results Reference
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IVF Treatment in Women With Immature Oocytes in Previous Cycle

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