Prognostic Value of Progesterone on Oocyte Retrieval Day... | NCT02109900

Studies
Prognostic Value of Progesterone on Oocyte Retrieval Day for In Vitro Fertilization Outcome

NCT02109900

Sponsor

Acibadem University

Status

Unknown status

Last Update Posted

Apr 10, 2014Estimated

Enrollment

180Estimated

Phase

Not provided

Conditions

Infertility
Assisted Reproductive Technology

Interventions

Serum Progesterone Levels

Countries

Not provided

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

Apr 2014

Overall Recruitment Status or Expanded Access Status

Unknown status

Last Known Status

Active, not recruiting

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Feb 2014

Primary Completion Date

Jun 2014Estimated

Completion Date

Not provided

First Submitted Date

Apr 7, 2014

First Submission Date that Met QC Criteria

Apr 8, 2014

First Posted Date

Apr 10, 2014Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

Apr 8, 2014

Last Update Posted Date

Apr 10, 2014Estimated

Description Module

Brief Summary

This observational study aims the potential role of serum progesterone levels on the day of oocyte pick-up on the probability of pregnancy, in patients undergoing antagonist IVF cycles.

There has been evidence, that increased serum levels of progesterone on triggering day are associated with a decreased probability of pregnancy after IVF.

There is no study that investigate assocation between serum progesterone levels on the day of oocyte pick-up and IVF outcomes. This study will be the first in this case.

Detailed Description

Not provided

Design Module

Study Type

Observational

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Target Follow-Up Duration

Not provided

Phases

Not provided

Interventional Study Design

Allocation

Not provided

Intervention Model

Biospecimen

No data available

No data is available for this block.

Enrollment

180Estimated

Label	Type	Description	Intervention Names
Serum Progesteron Levels			Other: Serum Progesterone Levels

Name	Type	Description	Arm Group Labels	Other Names
Serum Progesterone Levels	Other		Serum Progesteron Levels

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Clinical pregnancy	Clinical pregnancy, defined as ultrasound evidence of gestational sac at 6 weeks of gestation	At 6-8 weeks of gestation

Secondary Outcomes

Not provided

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Age < 40 years
Basal FSH < 12 IU/L
Basal P < 1.6 ng/mL

Exclusion Criteria:

Women with polycystic ovaries syndrome (PCOS)
Women with Stage III-IV Endometriosis
Women with a pathological condition of the adrenal glands

Accepts Healthy Volunteers

Yes

Sex

Female

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

39 Years

Standard Ages

Adult

Study Population

Patients who are referred to Acibadem Kayseri Hospital IVF Unit

Sampling Method

Probability Sample

Name	Affiliation	Role
Turgut Aydin	Acıbadem Kayseri Hospital	Principal Investigator

Condition Browse Module

MeSH Terms

ID	Term
D007246	Infertility

Ancestor Terms

ID	Term
D000091662	Genital Diseases
D000091642	Urogenital Diseases

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Browse Branches

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