ClinicalTrials.gg
RecruitingNCT06154954GenomicsUpdated Dec 4, 2023

Testicular Proteins for Sperm Retrieval Prediction Protein1, Testis-Expressed Gene 101, and Lectin Galactoside-binding Protein in Predicting Surgical Sperm Retrieval in Men With Non-Obstructive Azoospermia

An observational study in Non-obstructive Azoospermia, sponsored by Cairo University. Recruiting at 1 site in Egypt. Open to male participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-12-04.

Sponsored by Cairo University · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2023, 2 years 10 months ago, but the record still lists the study as recruiting.
  • Started Jun 2022; still recruiting 4 years 5 months later.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
90
Ages
18 Years and older
Sex
Male
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Study summary

Generally, azoospermia is characterized as obstructive (OA) or nonobstructive (NOA). Surgical spermatozoa retrieval results vary in success rates. Proposing Intracytoplasmic Sperm Injection (ICSI) to infertile couples with NOA depends on spermatogenesis, testicular histology, and the ability to extract live spermatozoa from testis biopsy pieces.

Unfortunately, only 50% of testicular sperm extraction (TESE) results are positive (Zarezadeh et al., 2021). Repeating sperm retrieval can cause TESE-induced hypoganadism, including reduced testicular volume, erectile dysfunction, and testosterone deficiency (Eliveld et al., 2018; Okada et al., 2002; Ozturk et al., 2011; Altinkilic et al., 2017; Akbal et al., 2017; Binsaleh et al., 2017). The prognostic efficacy of hormonal, molecular, cytological, and biochemical indicators for effective sperm recovery is limited (Corona et al., 2019). Molecular, biochemical, clinical, and histopathological characteristics that identify NOA males with advanced spermatogenesis foci up to the spermatozoon stage are crucial for therapeutic purposes.

Recent research suggests that seminal protein expression patterns change dramatically between azoospermic and fertile males (Zhang et al., 2021). TEX101 is a membrane protein only produced by testicular germ cells and shed into seminal plasma (SP). Research suggests that Tex101 malfunctions may impact male fertility (Jarvi et al., 2021). TEX101 is a germ cell mono-specific marker present on sperm, round spermatids, and spermatocytes. At a threshold of >5 ng/mL, TEX101 can distinguish NOA with Sertoli-cell only syndrome from other testis histologies, such as hypospermatogenesis (67% specificity, 100% sensitivity) or maturation arrest (54% sensitivity, 100% specificity) (Drabovich et al., 2013). ECM1, an epididymal mono-specific marker, was below detection limits in males with OA semen but present in detectable levels.

Research Template 3: Final Version: April 2019 NOA amounts in males. Clinical immunoassays of ECM1 and TEX101 can predict sperm retrieval outcomes for assisted reproduction and lower the cost of diagnosing azoospermia.

ELISA confirms that the lectin galactoside-binding, soluble 3 binding protein (LGALS3BP) is expressed throughout the male genital tract. Its physiological role in cell-to-cell interaction through extracellular matrix suggests a possible role in spermatogenesis, particularly in the late stage, despite not being a germ-cell specific marker (Cannarella et al., 2020). Patients with a good result of TESE had significantly greater levels of LGALS3BP in the SP. A cut-off of 153 ng/mL was observed with 100% sensitivity and 45% specificity. Freour et al. (2013) identified a key issue in their analysis due to the small number of instances (n=40) with lower AUC values. Araujo and Bertolla (2021) propose that LGALS3BP may predict TESE success in NOA patients before ICSI.

Read the detailed description

Azoospermia is mainly classified as obstructive azoospermia (OA) or nonobstructive azoospermia (NOA). Surgical retrieval of spermatozoa yields various success rates. The chance for proposing Intracytoplasmic Sperm Injection (ICSI) to infertile couple in case of NOA depends on spermatogenesis, testicular histology and on the possibility to retrieve live spermatozoa from testis biopsy fragments.

Unfortunately, this favorable outcome is obtained in only 50% of testicular sperm extraction (TESE) (Zarezadeh et al., 2021). Repeating the sperm retrieval procedure may lead to TESE induced hypoganadism (Eliveld et al., 2018) including the chance of reduced testicular volume (Okada et al., 2002, Ozturk et al., 2011, Altinkilic et al., 2017), the probability of erectile dysfunction (Akbal et al., 2017) and testosterone deficiency (Altinkilic et al., 2017, Binsaleh et al., 2017). Various hormonal, molecular, cytological, biochemical predictive parameters for successful sperm recovery offer limited predictive power (Corona et al., 2019). It is obvious that the establishment of molecular, biochemical, clinical or histopathological parameters that have a role in identifying subpopulations of NOA men positive for foci of advanced spermatogenesis, up to the spermatozoon stage, has great clinical importance. Recent studies demonstrated that the seminal protein expression pattern could differ significantly between azoospermic patients and fertile men (Zhang et al., 2021). Testis-expressed gene 101 (TEX101) is a cell membrane protein exclusively expressed by testicular germ cells and shed into seminal plasma (SP). There have been indications that the malfunction of Tex101 may affect male fertility (Jarvi et al., 2021). TEX101 is a germ cell mono-specific marker found on sperm, round spermatids, and spermatocytes. TEX101, at a threshold >5 ng/mL, could differentiate NOA underlined by Sertoli-cell only syndrome from NOA due to other testis histology (e.g., hypospermatogenesis, with a 67% specificity and a 100% sensitivity, or maturation arrest, with a 54% sensitivity and a 100% specificity) (Drabovich et al., 2013). ECM1 is an epididymal mono-specific marker which was below detection limits for men with OA, but present in the semen in detectable Research Template 3 Final Version: Ap ril 2019 amounts in men with NOA. Clinical immunoassays of extracellular matrix protein1 (ECM1) and TEX101 have the potential to facilitate prediction of the outcome of sperm retrieval procedures used for assisted reproduction, and reduce the total cost of azoospermia diagnosis. The lectin galactoside-binding, soluble 3 binding protein (LGALS3BP) is expressed in the whole male genital tract, with an expression level compatible with ELISA confirmation method, and because its physiological role in cell to cell interaction through extracellular matrix supports a possible role in spermatogenesis especially the late stage of spermatogenic activity, even if it is not a germ-cell specific marker (Cannarella et al., 2020). Significantly higher levels of lectingalactoside-binding, soluble 3 binding protein (LGALS3BP) in the SP were found in patients with a positive outcome of TESE. The cut-off of 153 ng/mL was reported with a sensitivity of 100% and a specificity of 45%. However, the limited number of cases (n=40) with a consequent lower AUC value represent a major flaw in that study (Freour et al., 2013). Araujo and Bertolla suggest that LGALS3BP could potentially be used as a predictive marker of success of TESE in NOA patients before ICSI (Araujo and Bertolla 2021).

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Conditions studied

  • Non-obstructive Azoospermia

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03

In context

Azoospermia

59 studies on the registry are indexed under Azoospermia; 17 are open to participants now.

This study's planned enrollment of 90 is close to the median of 95 across 24 observational studies indexed under Azoospermia.

Browse Azoospermia studies →

Lead sponsor

Cairo University is the lead sponsor of 4,941 studies on the registry; 1,458 are open to participants now.

Of its 37 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

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

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Who can participate

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

Study population

Azoospermic patients whom are scheduled for TESE operation attending at Andrology clinic, Kasr Al Ainy hospital.

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

  • Men with Non-obstructive azoospermia

Exclusion criteria

Exclusion Criteria:

  1. Sex reversal syndrome.
  2. Macro-deletion on the Y chromosome (To those accepting the chromosomal study)
  3. AZF a, AZF b microdeletion (To those accepting the Y chromosome microdeletion analysis).
  4. Obstructive azoospermia.
  5. Undescended testis.
  6. Hypogonadotrophic Hypogonadism
  7. Testicular procedures and operations -
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Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
90 participants (estimated)
Patient registry
No

Interventions

  • Diagnostic testSemen analysis

    Semen analysis for extracellular matrix proteins analysis

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What researchers measure

Primary outcomes

  1. Calculating the cut off level of the following markers a. ECM, b. TEX 101 and c. LAGALS3BP

    These proteins if present, they would provide the highest yield of sperms

    Time frame: 6 months

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Study locations

1 of 1 sites recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jun 2022 (actual). Primary completion is estimated for Dec 2023, 18 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 24, 2023
First posted
Dec 4, 2023
StartActual
Jun 1, 2022
Primary completionEst.
Dec 30, 2023
CompletionEst.
Mar 30, 2024
Last update
Dec 4, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Dec 4, 2023, 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
NCT06154954
Lead sponsor
Cairo University
Responsible party
Mohamed Wael Ragab (Lecturer, Cairo University) — Principal investigator
First posted
Dec 4, 2023
Start date
Jun 1, 2022
Primary completion
Dec 30, 2023 (estimated)
Completion
Mar 30, 2024 (estimated)
Last update
Dec 4, 2023

Oversight

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

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