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OpenTrials
Completed

NCT Number: NCT07286279

Identifying Candidates for Limited Dissection at Microdissection TESE.

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.

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Observational

Primary location

Clinique ovo

Montreal, Quebec, H4P 2S4, Canada

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

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

Treatment and study plan

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)

Sponsors and collaborators

Lead sponsor

Clinique Ovo

Industry

Registry information

Official study title

Identifying Infertile Men Who May be Amenable to a Limited Testicular Dissection at Microdissection Testicular Sperm Extraction

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Dec 16, 2025
Registry last updated
Feb 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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