Timing of Oocyte Retrieval and Micro Testicular Sperm Extraction
1 other identifier
observational
129
1 country
1
Brief Summary
This is a retrospective study to assess outcomes of micro-TESE performed 24 or 48 hours before oocyte retrieval and ICSI.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Nov 2025
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 15, 2025
CompletedFirst Submitted
Initial submission to the registry
November 17, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
November 30, 2025
CompletedFirst Posted
Study publicly available on registry
December 5, 2025
CompletedDecember 5, 2025
December 1, 2025
15 days
November 17, 2025
December 3, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of live births following ICSI with micro-TESE either 24 or 48 hours prior to oocyte retrieval
For IVF performed from June 2015 to January 2025
Secondary Outcomes (3)
Percentage of fertilized oocytes with two pronuclei (2PN)
For IVF performed from June 2015 to January 2025
Percentage of usable blastocyst (defined as frozen and transferred blastocysts)
For IVF performed from June 2015 to January 2025
Pregnancy rate based on positive β-hCG
For IVF performed from June 2015 to January 2025
Eligibility Criteria
Men who underwent a micro-TESE for IVF treatment
You may qualify if:
- Men who underwent a micro-TESE at the OVO clinic from June 2015 to January 2025.
- Patients with non-obstructive azoospermia (NOA), (absence of spermatozoa in multiple semen analyses)
- Patients with cryptozoospermia, (presence of a small number of spermatozoa detectable only after semen centrifugation)
- Patients with oligoasthenoteratozoospermia (OAT), (sperm concentration of less than 15 million/mL, reduced motility and abnormal morphology)
You may not qualify if:
- Patients who did not have any sperm noted following micro-TESE
- Use of donor sperm or oocytes
- Frozen sperm or oocytes
- Same day oocyte retrieval and sperm extraction
- Reversible cause of cryptozoospermia (i.e presence of a varicocele, febrile illness, or recent toxin exposure) Partial genital tract obstruction (i.e post-vaso-vasostomy, post-vasoepididymostomy, and low volume cryptozoospermia with ejaculatory duct obstruction)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Clinique Ovolead
Study Sites (1)
Clinique ovo
Montreal, Quebec, H4P 2S4, Canada
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Isaac-Jacques Kadoch, MD
Clinique Ovo
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 17, 2025
First Posted
December 5, 2025
Study Start
November 15, 2025
Primary Completion
November 30, 2025
Study Completion
November 30, 2025
Last Updated
December 5, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share