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Follicular Flushing Outcomes in Singles Versus Double Lumen Oocyte Retrieval Needles in Poor Responding Patients (needles(opu))

B

Baskent University

Status

Completed

Conditions

Infertility

Treatments

Procedure: single lumen needle in oocyte retrieval
Procedure: double lumen needle in oocyte retrieval

Study type

Interventional

Funder types

Other

Identifiers

NCT02391155
KA13/161

Details and patient eligibility

About

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.

Full 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

Enrollment

80 patients

Sex

Female

Ages

20 to 45 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 2 patient groups

single lumen
Active Comparator group
Description:
Single lumen needle in oocyte retrieval
Treatment:
Procedure: single lumen needle in oocyte retrieval
Procedure: double lumen needle in oocyte retrieval
double lumen
Active Comparator group
Description:
Double lumen needle with follicle flushing during oocyte retrieval
Treatment:
Procedure: single lumen needle in oocyte retrieval
Procedure: double lumen needle in oocyte retrieval

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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