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

Detailed Description

This study will include:

  1. women with less than four follicles on the day of hCG administration
  2. women between 20-45 age old
  3. 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:

  1. women between 20-45 years old
  2. the number of follicles less than 5 on the day of HCG administration
  3. the value of progesteron on the day of hCG administration must be under 1.5ng/ml

Exclusion Criteria:

  1. women under 20 years and older than 45 year
  2. on the day of hCG administration if the follicle number is more than 5
  3. 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.

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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