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Adjuvant Growth Therapy in in Vitro Fertilization

Primary Purpose

Infertility

Status
Completed
Phase
Phase 4
Locations
Canada
Study Type
Interventional
Intervention
Adjuvant Growth Hormon
Sponsored by
Clinique Ovo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring In vitro fertilization, Antagonist protocol, Growth Hormone

Eligibility Criteria

35 Years - 42 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women between the ages of 35 to 42
  • Primary or secondary infertility)

    • No previous treatment IVF cycle using the same proposed protocol
  • Negative pregnancy test at randomization (urine or blood)

Exclusion Criteria:

  • Contraindication to Saizen®
  • Simultaneous participation in another clinical trial
  • follicle stimulating hormone > 12 IU/L and/or anti-mullerian hormone < 0.5 pg/ml
  • Body mass index ≥ 35 kg/m2
  • Known risk of gestational diabetes
  • Administration of any investigational medication three months prior to study enrolment
  • Positive results of screening for either partner for HIV antibodies, Hepatitis B (other than surface antibodies present after vaccination) or Hepatitis C
  • Not able to communicate in French or English

Sites / Locations

  • Clinique Ovo

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Growth Hormon

Control

Arm Description

The participants randomized in the control group will be prescribed a regular antagonist IVF cycle with dose appropriate stimulation medication and will receive 2.5 mg of Adjuvant Growth Hormon (Saizen) daily via subcutaneous injections, from the beginning of the ovarian reserve stimulation until the day of the ovulation triggering.

The participants randomized in the control group will be prescribed a regular antagonist IVF cycle with dose appropriate stimulation medication without Adjuvant Growth Hormon (Saizen).

Outcomes

Primary Outcome Measures

Clinical pregnancy rate
To determine if the clinical pregnancy rate during the course of one treatment cycle in women receiving Growth Hormone daily in addition to gonadotropin-releasing hormone antagonist protocol is significantly higher than those receiving only gonadotropin-releasing hormone antagonist protocol (control group).

Secondary Outcome Measures

Total dose of gonadotropins
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Number of observed follicles
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Number of mature (Metaphase II) oocytes retrieved
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Oocyte morphology
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Fertilization rate
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Embryo morphology
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Embryo cleavage rate
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Number of embryos available
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Number of supernumerary embryos available for cryopreservation
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Implantation rate
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Miscarriage rate
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Live birth rate
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Adverse side effects in women
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.

Full Information

First Posted
October 24, 2012
Last Updated
January 7, 2022
Sponsor
Clinique Ovo
Collaborators
EMD Serono
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1. Study Identification

Unique Protocol Identification Number
NCT01715324
Brief Title
Adjuvant Growth Therapy in in Vitro Fertilization
Official Title
Adjuvant Growth Therapy in in Vitro Fertilization: A Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
June 25, 2014 (Actual)
Primary Completion Date
July 2021 (Actual)
Study Completion Date
August 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Clinique Ovo
Collaborators
EMD Serono

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
In an In Vitro Fertilization (IVF) cycle super ovulating drugs (gonadotropins) are usually taken to stimulate the ovaries to produce more than one egg. In Vitro Fertilization protocols are constantly under review in order to improve the recruitment of the follicles, which contain the eggs, whilst minimizing the doses of gonadotrophins required, with the ultimate aim of increasing the live birth rate.
Detailed Description
The addition of growth hormone, which is a biological hormone that can be synthetically produced, as a supplement to gonadotrophins in an In Vitro Fertilization cycle has been suggested as a way in which In Vitro Fertilization pregnancy rates may be increased.Growth hormone has been shown, in animal and human studies, to be important in the recruitment of follicles.However, to date, only a limited number of clinical studies have been performed in order to assess whether the addition of growth hormone can improve the probability of pregnancy in women undergoing ovarian stimulation for In Vitro Fertilization. As the total number of patients analysed in these studies was small it has not been possible to determine whether if there is any improvement the outcome of an In Vitro Fertilization cycle when a woman is given growth hormone therapy as a supplement during her treatment. This goal of this study is to determine the effectiveness of using growth hormone therapy as a supplement to the administration of gonadotropins in an antagonist In Vitro Fertilization protocol.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
In vitro fertilization, Antagonist protocol, Growth Hormone

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
288 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Growth Hormon
Arm Type
Experimental
Arm Description
The participants randomized in the control group will be prescribed a regular antagonist IVF cycle with dose appropriate stimulation medication and will receive 2.5 mg of Adjuvant Growth Hormon (Saizen) daily via subcutaneous injections, from the beginning of the ovarian reserve stimulation until the day of the ovulation triggering.
Arm Title
Control
Arm Type
No Intervention
Arm Description
The participants randomized in the control group will be prescribed a regular antagonist IVF cycle with dose appropriate stimulation medication without Adjuvant Growth Hormon (Saizen).
Intervention Type
Drug
Intervention Name(s)
Adjuvant Growth Hormon
Other Intervention Name(s)
Saizen
Intervention Description
The treatment group will receive 2.5 mg of Saizen daily via subcutaneous injections, from the beginning of the ovarian reserve stimulation until the day of the ovulation triggering
Primary Outcome Measure Information:
Title
Clinical pregnancy rate
Description
To determine if the clinical pregnancy rate during the course of one treatment cycle in women receiving Growth Hormone daily in addition to gonadotropin-releasing hormone antagonist protocol is significantly higher than those receiving only gonadotropin-releasing hormone antagonist protocol (control group).
Time Frame
7 weeks
Secondary Outcome Measure Information:
Title
Total dose of gonadotropins
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks
Title
Number of observed follicles
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks
Title
Number of mature (Metaphase II) oocytes retrieved
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks
Title
Oocyte morphology
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks
Title
Fertilization rate
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks
Title
Embryo morphology
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks
Title
Embryo cleavage rate
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks
Title
Number of embryos available
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks
Title
Number of supernumerary embryos available for cryopreservation
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks
Title
Implantation rate
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks
Title
Miscarriage rate
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
40 weeks
Title
Live birth rate
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
40 weeks
Title
Adverse side effects in women
Description
To evaluate the effectiveness of Growth Hormon adjuvant therapy in gonadotropin-releasing hormone antagonist protocol when compared to the control group.
Time Frame
7 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
42 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women between the ages of 35 to 42 Primary or secondary infertility) No previous treatment IVF cycle using the same proposed protocol Negative pregnancy test at randomization (urine or blood) Exclusion Criteria: Contraindication to Saizen® Simultaneous participation in another clinical trial follicle stimulating hormone > 12 IU/L and/or anti-mullerian hormone < 0.5 pg/ml Body mass index ≥ 35 kg/m2 Known risk of gestational diabetes Administration of any investigational medication three months prior to study enrolment Positive results of screening for either partner for HIV antibodies, Hepatitis B (other than surface antibodies present after vaccination) or Hepatitis C Not able to communicate in French or English
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jacques Kadoch, MD
Organizational Affiliation
Clinique Ovo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Clinique Ovo
City
Montreal
State/Province
Quebec
ZIP/Postal Code
H4P 2S4
Country
Canada

12. IPD Sharing Statement

Citations:
PubMed Identifier
34808697
Citation
Sood A, Mohiyiddeen G, Ahmad G, Fitzgerald C, Watson A, Mohiyiddeen L. Growth hormone for in vitro fertilisation (IVF). Cochrane Database Syst Rev. 2021 Nov 22;11(11):CD000099. doi: 10.1002/14651858.CD000099.pub4.
Results Reference
derived

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Adjuvant Growth Therapy in in Vitro Fertilization

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