Prognostic Value of Progesterone on Oocyte Retrieval Day for In Vitro Fertilization Outcome
NCT ID: NCT02109900
Last Updated: 2014-04-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
180 participants
OBSERVATIONAL
2014-02-28
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
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.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Prognostic Value of Progesterone for In Vitro Fertilization (IVF) Outcome
NCT01067664
Predictive Value of Mid-luteal Serum Progesterone Levels in Egg Donation Cycles
NCT02696694
Progesterone on the Day of Ovulation Induction is Associated With Pregnancy Outcome
NCT01426152
Progesterone Rise in Agonist Versus Antagonist in Vitro Fertilization (IVF) Cycles
NCT01191710
Assessment of Two Methods for Progesterone Dosage During IVF
NCT05987657
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Serum Progesteron Levels
Serum Progesterone Levels
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Serum Progesterone Levels
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Basal FSH \< 12 IU/L
* Basal P \< 1.6 ng/mL
Exclusion Criteria
* Women with Stage III-IV Endometriosis
* Women with a pathological condition of the adrenal glands
18 Years
39 Years
FEMALE
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Acibadem University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Turgut Aydın
Specialist, Gynecology and Obstetrics
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Turgut Aydin
Role: PRINCIPAL_INVESTIGATOR
Acıbadem Kayseri Hospital
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
OpudayPivfOutcome
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.