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CompletedNCT00484081Updated Jun 8, 2007

Microdissection Testicular Sperm Extraction (MicroTESE) and IVF-ICSI Outcome in Non-Obstructive Azoospermia (NOA)

An interventional study of Microdissection Testicular Sperm Extraction and ICSI in Azoospermia and Infertility, sponsored by Clinic and Research Center in Human Reproduction Roger Abdelmassih. Completed at 1 site in Brazil. Per ClinicalTrials.gov, last updated 2007-06-08.

Sponsored by Clinic and Research Center in Human Reproduction Roger Abdelmassih · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
53
Allocation
Not applicable
Sex
All
01

Study summary

We evaluated the application of surgical testicular exploration with the aid of a microscope (MictoTESE) to increase the chances of obtaining sperm in men with impaired sperm production, a condition known as non-obstructive azoospermia.

We also evaluated the outcomes of these couples when the sperm obtained were used in ICSI (Intracytoplasmic Sperm Injection) during assisted reproductive technology treatment.

We believe that excellent results may be obtained with the use of the following techniques in the treatment of couples where non-obstructive azoospermia is a significant cause.

Read the detailed description

Men diagnosed with non-obstructive azoospermia and seeking assisted reproductive technology treatment (ART) are candidates for surgical sperm retrieval with the aid of microdissection. We believe that this approach may currently be the best option for these subjects.

We evaluated our surgical sperm retrieval rate associated to their serum LH, FSH, TOTAL TESTOTERONE and PROLACTIN levels, pre-operative testicular volume and also compared to the post-operative histological analysis of fixed testicular tissue specimens collected during the procedure, stained with haematoxylin and eosin.

We also evaluated the outcomes using ICSI based ART for these couples observing mean ICSI and fertilized oocytes, number and quality of embryos transferred, implantation and pregnancy rates.

02

Conditions studied

  • Azoospermia
  • Infertility

Keywords

  • TESE
  • NON-OBSTRUCTIVE
  • MICRODISSECTION
  • AZOOSPERMIA
  • ICSI
03

In context

Infertility

2,506 studies on the registry are indexed under Infertility; 407 are open to participants now.

This study's enrollment of 53 is below the median of 120 across 1,698 interventional studies indexed under Infertility.

Browse Infertility studies →

Lead sponsor

Clinic and Research Center in Human Reproduction Roger Abdelmassih is the lead sponsor of 2 studies on the registry; none are open to participants now.

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

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Men undergoing ART treatment with clinical diagnosis of non-obstructive azoospermia.
  • Female partner undergoing ICSI based ART treatment

Exclusion criteria

Exclusion Criteria:

  • Men where non-obstructive azoospermia was not confirmed based on histological analysis of fixed testicular tissue specimens collected by open surgical testicular biopsy and stained with haematoxylin and eosin.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
53 participants (actual)

Interventions

  • ProcedureMicrodissection Testicular Sperm Extraction
  • ProcedureICSI
06

What researchers measure

Primary outcomes

  1. Sperm retrieval rate,mean male and female partner age,mean ICSI and fertilized oocytes, implantation, pregnancy and miscarriage rates.Testicular histology was also compared.

    Time frame: 17 months

Secondary outcomes

  1. Sperm retrieval associated to pre-operative serum FSH, LH, Total Testosterone,Prolactin, testicular volume and post-operative testicular histology. ICSI and pregnancy results associated to sperm motility.

    Time frame: 17 months

07

Study locations

1 site
  • Clinic and Research Center in Human Reproduction Roger Abdelmassih
    São Paulo, SP 01431-000, Brazil
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 8, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00484081
Lead sponsor
Clinic and Research Center in Human Reproduction Roger Abdelmassih
First posted
Jun 8, 2007
Start date
Jun 2005
Completion
Oct 2006
Last update
Jun 8, 2007

Study contacts

Pedro Ravizzini, Dr.
principal investigator · Clinic and Research Center in Human Reproduction Roger Abdelmassih

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2007. You cannot join it, but the record below documents what was studied.

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