- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02391155
Follicular Flushing Outcomes in Singles Versus Double Lumen Oocyte Retrieval Needles in Poor Responding Patients (needles(opu))
June 29, 2018 updated by: Bulent Haydardedeoglu, Baskent University
Follicular Flushing Outcomes in Singles Versus Double Lumen Oocyte Retrieval Needles in Poor Responding Patients:a Randomized Controlled Trial
In this study, the investigators aimed to evaluate to the efficacy of the needle type used in follicular flushing in oocyte retrieval in the poorest responders undergoing IVF.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
This study will include:
- women with less than four follicles on the day of hCG administration
- women between 20-45 age old
- The value of progesterone on the day of hCG administration will be under 1.5ng/ml
Study Type
Interventional
Enrollment (Actual)
80
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Adana, Turkey, 01120
- Bulent Haydardedeoglu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 45 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- women between 20-45 years old
- the number of follicles less than 5 on the day of HCG administration
- the value of progesteron on the day of hCG administration must be under 1.5ng/ml
Exclusion Criteria:
- women under 20 years and older than 45 year
- on the day of hCG administration if the follicle number is more than 5
- if.the value of progesteron on the day of hCG administration is higher than 1.5ng/ml
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: single lumen
Single lumen needle in oocyte retrieval
|
single lumen needle use during oocyte retrieval
after aspiration of follicles, 3 times flushing will be performed in double lumen needle.
|
Active Comparator: double lumen
Double lumen needle with follicle flushing during oocyte retrieval
|
single lumen needle use during oocyte retrieval
after aspiration of follicles, 3 times flushing will be performed in double lumen needle.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
number of metaphase 2 oocyte
Time Frame: Six months
|
Six months
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
clinical pregnancy rate
Time Frame: eigth months
|
eigth months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2015
Primary Completion (Actual)
July 1, 2015
Study Completion (Actual)
July 1, 2015
Study Registration Dates
First Submitted
February 11, 2015
First Submitted That Met QC Criteria
March 11, 2015
First Posted (Estimate)
March 18, 2015
Study Record Updates
Last Update Posted (Actual)
July 2, 2018
Last Update Submitted That Met QC Criteria
June 29, 2018
Last Verified
March 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KA13/161
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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