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Heated and Non Heated Ovarian Aspiration Needle Protocol

Primary Purpose

Infertility, Female

Status
Recruiting
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
warming of the follicular aspiration needle
Sponsored by
Hospital de Clinicas de Porto Alegre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Infertility, Female

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: All women submitted to IVF cycles Exclusion Criteria: Women submitted to follicular aspiration due to oocyte cryopreservation Patients without oocyte retrieved Patients without mature oocyte retrieved Procedures with needle replacement

Sites / Locations

  • Insemine Human Reproduction CentreRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Standard protocol

Warming protocol

Arm Description

The standard protocol comprises no heating of the aspiration needle.

The aspiration needle will be warm-up overnight the day before the oocyte pick-up procedure

Outcomes

Primary Outcome Measures

normal fertilization rate
Fertilization will be confirmed through the visualization of the presence of two pronuclei

Secondary Outcome Measures

number of oocyte retrieved
the total number of oocytes captured in the ovarian aspiration procedure
number of mature oocyte
total number of MII
oocyte damage rate
the number of fractured oocytes or atresia
abnormal fertilization rate
the total number of zygotes with three or more pronuclei

Full Information

First Posted
December 22, 2022
Last Updated
March 2, 2023
Sponsor
Hospital de Clinicas de Porto Alegre
Collaborators
Guedes da Luz Médicos Associados Sociedade Simples LTDA
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1. Study Identification

Unique Protocol Identification Number
NCT05683639
Brief Title
Heated and Non Heated Ovarian Aspiration Needle Protocol
Official Title
Randomized Clinical Trial in Women Submitted to in Vitro Fertilization: Warming Versus Not Warming of the Follicular Aspiration Needle.
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 1, 2022 (Actual)
Primary Completion Date
March 1, 2023 (Anticipated)
Study Completion Date
June 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospital de Clinicas de Porto Alegre
Collaborators
Guedes da Luz Médicos Associados Sociedade Simples LTDA

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
The success of IVF is influenced by factors as cause of infertility and age. Furthermore, there is a large influence of external factors, from the laboratory environment, handling and cultivation of gametes and embryos. The existence of factors capable of affecting the success of the treatment lead to the need of a quality control to attenuate the unfavorable effects. After ovarian stimulation, follicular aspiration is performed. At this moment, factors such as aspiration technique, needle type and temperature are the main variables to be controlled. It is known that oocytes are the more sensitive cells to temperature fluctuations. Currently, the standard protocol for follicular aspiration does not include the warming of the aspiration needle. However, due to the existing evidence in the literature, that the follicular fluid temperature drops during the aspiration procedure, this work aims to evaluate the influence of a pre warming of the aspiration needle as a new protocol.
Detailed Description
The estimated sample was 600 oocytes for each group, totaling a minimum of 1200 oocytes, considering a fertilization rate of 65% in the control group and 73% in the study group, for a power of 80% and p alpha 5%, i.e. , an increase of more than 10% between groups. As there is no data in the literature, when the investigators have this sample an interim analysis to evaluate the data will be performed. The investigators consider 10% a reasonable difference that can (with this sample size) increase by 48 embryos and a possible increase of 7 pregnancies within this sample. Bearing in mind that the average number of oocytes retrieved per patient is 6 oocytes, the investigators estimate that 200 patients will be needed to reach the calculated sample number. The warm-up protocol will be applied by the embryologists, which consists of heating the follicular aspiration needle to 37 Celsius, overnight, the day before the day of the ovarian aspiration procedure. The variables that will be compared between the studied groups are the rates of oocyte retrieval, maturity (MII), fracture, atresia, fertilization rates and discarded embryos. Continuous variables will be analyzed using Student's t test if they have normal distribution, for comparison of means between two independent groups or the Wilcoxon-Mann-Whitney U test if not parametric. Differences between groups will be considered significant when p<0.05.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Female

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Standard protocol
Arm Type
No Intervention
Arm Description
The standard protocol comprises no heating of the aspiration needle.
Arm Title
Warming protocol
Arm Type
Experimental
Arm Description
The aspiration needle will be warm-up overnight the day before the oocyte pick-up procedure
Intervention Type
Other
Intervention Name(s)
warming of the follicular aspiration needle
Intervention Description
the follicular aspiration needle will be heated overnight before the ovarian aspiration procedure.
Primary Outcome Measure Information:
Title
normal fertilization rate
Description
Fertilization will be confirmed through the visualization of the presence of two pronuclei
Time Frame
16 to 18 hours after fertilization procedure
Secondary Outcome Measure Information:
Title
number of oocyte retrieved
Description
the total number of oocytes captured in the ovarian aspiration procedure
Time Frame
immediately after ovarian aspiration procedure
Title
number of mature oocyte
Description
total number of MII
Time Frame
3 hours post ovarian aspiration
Title
oocyte damage rate
Description
the number of fractured oocytes or atresia
Time Frame
3 hours post ovarian aspiration
Title
abnormal fertilization rate
Description
the total number of zygotes with three or more pronuclei
Time Frame
16 to 18 hours after fertilization procedure

10. Eligibility

Sex
Female
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All women submitted to IVF cycles Exclusion Criteria: Women submitted to follicular aspiration due to oocyte cryopreservation Patients without oocyte retrieved Patients without mature oocyte retrieved Procedures with needle replacement
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lisiane Knob de Souza, MSc
Phone
+5551981625760
Email
lisiane@insemine.com
First Name & Middle Initial & Last Name or Official Title & Degree
Bruna Campos Galgaro, MSc
Phone
+5551991178290
Email
bruna@insemine.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
João da Cunha Filho, PhD
Organizational Affiliation
Hospital de Clínicas de Porto Alegre
Official's Role
Study Director
Facility Information:
Facility Name
Insemine Human Reproduction Centre
City
Porto Alegre
State/Province
Rio Grande Do Sul
ZIP/Postal Code
91330-001
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
João da Cunha Filho, phd
Phone
555133311388
Email
sabino@insemine.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Heated and Non Heated Ovarian Aspiration Needle Protocol

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