ClinicalTrials.gg
CompletedNCT07286279Updated Feb 27, 2026

Identifying Candidates for Limited Dissection at Microdissection TESE.

An observational study in Non Obstructive Azoospermia, Cryptozoospermia and Oligoasthenoteratozoospermia, sponsored by Clinique Ovo. Completed at 1 site in Canada. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-27.

Sponsored by Clinique Ovo · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
248
Ages
18 Years and older
Sex
Male
01

Study summary

The goal of this retrospective observational study is to learn whether certain clinical characteristics can help predict which infertile men may successfully have sperm retrieved using a less-invasive "mini-incision" version of micro-TESE. The study focuses on men with very low or absent sperm counts (non-obstructive azoospermia, cryptozoospermia, or severe OAT).

The main questions it aims to answer are:

Can sperm be successfully found using only a small, limited-dissection micro-TESE in some men?

Which clinical factors (such as hormone levels or medical history) help identify men who may benefit from this less-invasive approach?

Researchers will compare men who had successful sperm retrieval with the mini-incision alone to men who required a more extensive micro-TESE to see if certain characteristics predict which approach is likely to work.

Read the detailed description

This retrospective cohort study evaluates whether preoperative clinical characteristics can help identify infertile men who are likely to achieve successful sperm retrieval through a limited-dissection, mini-incision micro-TESE. The stepwise surgical approach begins with a small equatorial incision for targeted micro-biopsies and is expanded only when sperm are not initially identified.

The study includes men who underwent their first micro-TESE at a high-volume fertility center over a 10-year period. All procedures followed a standardized surgical protocol and were performed by a single experienced surgeon, ensuring uniformity in technique.

Clinical data routinely collected before surgery, such as hormone levels, semen parameters, testicular volume, and relevant medical history, were analyzed and compared between men who required only the mini-incision and those who proceeded to an extended dissection. By examining these differences, the study aims to determine whether certain patient characteristics can predict the success with the less-invasive approach.

The findings may help guide pre-surgical counseling and support more tailored surgical planning for men with severe male factor infertility

02

Conditions studied

  • Non Obstructive Azoospermia
  • Cryptozoospermia
  • Oligoasthenoteratozoospermia
  • Male Infertility

Keywords

  • micro-TESE
  • male infertility
  • non-obstructive azoospermia
  • cryptozoospermia
  • oligoasthenoteratozoospermia
  • mini-incision
03

In context

Oligospermia

64 studies on the registry are indexed under Oligospermia; 17 are open to participants now.

This study's enrollment of 248 is below the median of 300 across 17 observational studies indexed under Oligospermia.

Browse Oligospermia studies →

Lead sponsor

Clinique Ovo is the lead sponsor of 36 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Male
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Men who underwent micro-TESE procedure from March 2015 to June 2025

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients with cryptozoospermia or non obstructive azoospermia that underwent a micro-TESE

Exclusion criteria

Exclusion Criteria:

  • Patients with a potentially reversible cause of cryptozoospermia (i.e., presence of a varicocele, febrile illness, or recent toxin exposure)
  • Patients with suspected partial genital tract obstruction (i.e post-vaso-vasostomy, post-vasoepididymostomy, and low volume cryptozoospermia with ejaculatory duct obstruction)
  • Patients who have previously undergone a micro-TESE, TESA or TESE procedure
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
248 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Successful sperm retrieval rate defined as the presence of spermatozoa during limited dissection (mini-incision) micro-TESE

    Time frame: At the time of limited dissection (mini-incision)

Secondary outcomes

  1. Serum FSH levels

    Time frame: At baseline

  2. Serum testosterone levels

    Time frame: At baseline

  3. Testicular volume

    Time frame: At baseline

  4. Genetic abnormalities rate

    Time frame: At baseline

  5. Procedure conversion from limited to extensive micro-TESE rate

    Time frame: At the time of limited dissection (mini-incision)

07

Study locations

1 site
  • Clinique ovo
    Montreal, Quebec H4P 2S4, Canada
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07286279
Lead sponsor
Clinique Ovo
Responsible party
Sponsor
First posted
Dec 16, 2025
Start date
Dec 15, 2025
Primary completion
Dec 31, 2025
Completion
Jan 15, 2026
Last update
Feb 27, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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