Perifollicular Doppler in Natural Cycle In Vitro Fertilization

NCT ID: NCT01668212

Last Updated: 2013-06-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

160 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-03-31

Brief Summary

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Perifollicular Doppler could reflect the quality of the follicle's vascularization and, consequently, the one of the oocyte that ensues from it. Perifollicuar Doppler is the analysis, in ultrasound, of the blood flow in vessels surrounding the follicle.

The goal of this study is to evaluate if there is a link, in natural cycle In Vitro Fertilization, between the quality of the vascularization and the one of the oocyte, the embryo and the pregnancy.

Detailed Description

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Conditions

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Infertility

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

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natural In Vitro Fertilization cycle

Patient doing following natural In Vitro fertilization cycle

Doppler ultrasound

Intervention Type PROCEDURE

Doppler Ultrasound

Interventions

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Doppler ultrasound

Doppler Ultrasound

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patient with a natural In Vitro Fertilization cycle.
* Patient under 38 years old
* Body mass indice under 35
* Ovulatory cycles between 20-35 days

Exclusion Criteria

* Patient with a stimulation In Vitro Fertilization cycle
* Patient with a naturalIn Vitro Fertilization cycle with egg donor
* Patient with a natural In Vitro Fertilization cycle with freezing embryo
* Smoking patient
* Diabetic patient
* Patient with treatment of antihypertensive drug, anticoagulant, antiplatelet, vasodilator
* Body mass indice over 35
* Patient over 38 years old
* Patient without ovulation or cycle over 35 days
* Percutaneous Epididymal Sperm Aspiration (PESA), Testicular Sperm Extraction (TESE) or micro TESE
Minimum Eligible Age

18 Years

Maximum Eligible Age

38 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Clinique Ovo

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Delphine Delrieu, MD

Role: PRINCIPAL_INVESTIGATOR

Clinique Ovo

Locations

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Ovo Fertilité

Montreal, Quebec, Canada

Site Status

Countries

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Canada

Other Identifiers

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OVO-11-01

Identifier Type: -

Identifier Source: org_study_id

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