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Clomifene Citrate as First Line Treatment in in Vitro Fertilization Cycles for Patients With Lower Ovarian Reserve (clomid)

Primary Purpose

Infertility

Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
Clomifene Citrate
GnRH analog and recombinant human FSH
Sponsored by
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring ovarian reserve, ovarian stimulation, clomifene citrate, high doses Follicle Stimulating Hormone (FSH)

Eligibility Criteria

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

Inclusion Criteria:

  • age 18-42 years
  • infertility status
  • Day 3 serum FSH > 12 IU/ml in at least two occasions or previous poor response (≤3 oocytes retrieved) to hyper-stimulation

Exclusion Criteria:

  • contraindications to infertility treatments or pregnancy

Sites / Locations

  • Fondazione Ca' Granda Ospedale Maggiore Policlinico

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

High doses

Clomid

Arm Description

Administration of high doses of gonadotrophins to stimulate ovarian follicular growth

Administration of Clomiphene Citrate to obtain ovarian follicular growth

Outcomes

Primary Outcome Measures

live birth rate
general "Live birth rate" will be recorded at the end of the study when all participants have performed their In vitro Fertilization (IVF) treatment. Live birth rate per single patients will be recorded 4 weeks after embryo transfer when a intrauterine gestational sac is expected to be seen in case of pregnancy.

Secondary Outcome Measures

ratio pregnancies/costs
at the end of the study the number of obtained pregnancies will be divided by the total costs of treatments in two groups. A cost in euros will be therefore estimated for every single pregnancy in both groups.

Full Information

First Posted
July 1, 2011
Last Updated
July 11, 2011
Sponsor
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Collaborators
Istituto Clinico Humanitas, IRCCS San Raffaele, Istituti Clinici Zucchi
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1. Study Identification

Unique Protocol Identification Number
NCT01389713
Brief Title
Clomifene Citrate as First Line Treatment in in Vitro Fertilization Cycles for Patients With Lower Ovarian Reserve
Acronym
clomid
Official Title
Patients With Reduced Ovarian Reserve and In Vitro Fertilization (IVF) Cycles. A Randomized Multicentric Comparison of a Protocol With High Doses of Gonadotropins and a Protocol With Clomiphene Citrate Only. Evaluation of Clinical Effectiveness and Economic Issues
Study Type
Interventional

2. Study Status

Record Verification Date
July 2011
Overall Recruitment Status
Completed
Study Start Date
September 2008 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
December 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico
Collaborators
Istituto Clinico Humanitas, IRCCS San Raffaele, Istituti Clinici Zucchi

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Women with compromised ovarian reserve requiring in vitro fertilization (IVF) still represent a demanding challenge for clinicians. It has classically been claimed that using higher dosages of gonadotropins may overcome the scarce ovarian responsiveness to hyper-simulation and increase the chances of success. However, scientific evidence supporting this view is scanty and costs are inevitably much higher. In this study, the investigators hypothesized that similar chances of pregnancy may be achieved with a mild stimulation using exclusively Clomiphene citrate (CC).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
Keywords
ovarian reserve, ovarian stimulation, clomifene citrate, high doses Follicle Stimulating Hormone (FSH)

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
High doses
Arm Type
Active Comparator
Arm Description
Administration of high doses of gonadotrophins to stimulate ovarian follicular growth
Arm Title
Clomid
Arm Type
Experimental
Arm Description
Administration of Clomiphene Citrate to obtain ovarian follicular growth
Intervention Type
Drug
Intervention Name(s)
Clomifene Citrate
Other Intervention Name(s)
clomid
Intervention Description
3x50 mg die for 5 days from day 3 to day 7 of the menstrual cycle
Intervention Type
Drug
Intervention Name(s)
GnRH analog and recombinant human FSH
Other Intervention Name(s)
decapeptyl, Gonal-F
Intervention Description
daily subcutaneous 0.1 mg decapeptyl from day 1-2 of the menstrual cycle and recombinant human FSH 450 IU/die from day 3.
Primary Outcome Measure Information:
Title
live birth rate
Description
general "Live birth rate" will be recorded at the end of the study when all participants have performed their In vitro Fertilization (IVF) treatment. Live birth rate per single patients will be recorded 4 weeks after embryo transfer when a intrauterine gestational sac is expected to be seen in case of pregnancy.
Time Frame
end of the study (28 months)
Secondary Outcome Measure Information:
Title
ratio pregnancies/costs
Description
at the end of the study the number of obtained pregnancies will be divided by the total costs of treatments in two groups. A cost in euros will be therefore estimated for every single pregnancy in both groups.
Time Frame
end of the study (28 months)

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: age 18-42 years infertility status Day 3 serum FSH > 12 IU/ml in at least two occasions or previous poor response (≤3 oocytes retrieved) to hyper-stimulation Exclusion Criteria: contraindications to infertility treatments or pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
guido ragni, md
Organizational Affiliation
Fondazione Ca' Granda Ospedale Maggiore Policlinico
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fondazione Ca' Granda Ospedale Maggiore Policlinico
City
Milan
ZIP/Postal Code
20122
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
17336650
Citation
Heijnen EM, Eijkemans MJ, De Klerk C, Polinder S, Beckers NG, Klinkert ER, Broekmans FJ, Passchier J, Te Velde ER, Macklon NS, Fauser BC. A mild treatment strategy for in-vitro fertilisation: a randomised non-inferiority trial. Lancet. 2007 Mar 3;369(9563):743-749. doi: 10.1016/S0140-6736(07)60360-2.
Results Reference
background
PubMed Identifier
16239317
Citation
Eijkemans MJ, Heijnen EM, de Klerk C, Habbema JD, Fauser BC. Comparison of different treatment strategies in IVF with cumulative live birth over a given period of time as the primary end-point: methodological considerations on a randomized controlled non-inferiority trial. Hum Reprod. 2006 Feb;21(2):344-51. doi: 10.1093/humrep/dei332. Epub 2005 Oct 20.
Results Reference
background
PubMed Identifier
23249758
Citation
Ragni G, Levi-Setti PE, Fadini R, Brigante C, Scarduelli C, Alagna F, Arfuso V, Mignini-Renzini M, Candiani M, Paffoni A, Somigliana E. Clomiphene citrate versus high doses of gonadotropins for in vitro fertilisation in women with compromised ovarian reserve: a randomised controlled non-inferiority trial. Reprod Biol Endocrinol. 2012 Dec 18;10:114. doi: 10.1186/1477-7827-10-114.
Results Reference
derived

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Clomifene Citrate as First Line Treatment in in Vitro Fertilization Cycles for Patients With Lower Ovarian Reserve

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