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Not yet recruitingNCT07684963Updated Jul 6, 2026

Effect of Varicocelectomy on Spermatogenic Cell Count and Semen Parameters

An interventional study of Subinguinal Microsurgical Varicocelectomy in Varicocele, Male Infertility and Infertility, sponsored by Assiut University. Not yet recruiting. Open to male participants aged 20 Years to 45 Years. Per ClinicalTrials.gov, last updated 2026-07-06.

Sponsored by Assiut University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Not applicable
Ages
20 Years to 45 Years
Sex
Male
01

Study summary

This study aims to evaluate how varicocele surgery (varicocelectomy) affects the number of immature sperm cells (spermatogenic cells) found in the semen of infertile men. Varicocele, an abnormal dilation of veins in the scrotum, is a common cause of male infertility that can negatively impact semen quality and overall testicular function. While surgery is widely performed to improve standard semen parameters, this study specifically investigates its impact on the shedding of immature germ cells into the seminal fluid, which can be an indicator of impaired sperm production.

Researchers will enroll 40 infertile married men, aged 20 to 45, who have been diagnosed with a clinical varicocele and exhibit abnormal semen parameters. All participants will undergo a single surgical intervention known as a subinguinal microsurgical varicocelectomy. To measure the effects of the surgery, participants will undergo careful semen analysis before the procedure, and again at 3 and 6 months postoperatively. The primary goal is to track changes in the spermatogenic cell count and abnormal sperm morphology, and to explore how these changes correlate with conventional semen parameters like sperm concentration, motility, and vitality.

Read the detailed description

Male factor infertility contributes as the sole factor in approximately 20-25% of infertile couples. While semen analysis remains the cornerstone for evaluating male infertility , conventional parameters may not fully reflect underlying functional and molecular alterations. Varicocele, characterized by abnormal dilatation and tortuosity of the pampiniform venous plexus, is one of the most common correctable causes of male infertility. The pathological changes associated with varicocele can adversely affect the seminiferous epithelium, leading to defective spermatogenesis and an increased sloughing of immature germ cells (spermatogenic cells) into the seminal fluid. According to World Health Organization (WHO) recommendations, the presence of these spermatogenic cells is clinically relevant as it reflects impaired spermatogenesis and testicular dysfunction.

This prospective interventional study aims to evaluate changes in seminal spermatogenic cell counts and conventional semen parameters following surgical correction. Participants will undergo a subinguinal microsurgical varicocelectomy. During the procedure, the spermatic cord is delivered and examined under 5-10X microscopic magnification. The internal spermatic artery is carefully identified, utilizing an intraoperative USG probe if necessary, and dissected free of surrounding structures. Internal spermatic veins and cremasteric veins are ligated, while testicular arteries, cremasteric arteries, lymphatic vessels, and the vas deferens are preserved.

To assess the surgical outcomes, semen samples will be collected after 3-5 days of sexual abstinence preoperatively (at least a week apart, utilizing the second sample) and postoperatively at 3 and 6 months. The differentiation of seminal round cells into leukocytes and spermatogenic cells will be conducted using combined morphological and enzymatic methods. Semen smears will be stained with Papanicolaou stain and examined under light microscopy to identify spermatogenic cells based on nuclear morphological features. A peroxidase (Endtz) test will concurrently be used to differentiate peroxidase-positive leukocytes from peroxidase-negative spermatogenic cells. The spermatogenic cell concentration will be quantified using a Neubauer hemocytometer according to the WHO 2021 manual equation.

02

Conditions studied

  • Varicocele
  • Male Infertility
  • Infertility
  • Varicocelectomy

Keywords

  • Spermatogenic Cells
  • Semen Parameters
  • Immature Germ Cells
  • Semen Analysis
  • Sperm Morphology
  • Round Cells
03

In context

Varicocele

53 studies on the registry are indexed under Varicocele; 15 are open to participants now.

This study's planned enrollment of 40 is below the median of 72 across 36 interventional studies indexed under Varicocele.

Browse Varicocele studies →

Lead sponsor

Assiut University is the lead sponsor of 5,078 studies on the registry; 2,178 are open to participants now.

Of its 14 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

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

04

Who can participate

Ages eligible
20 Years to 45 Years
Sexes eligible
Male
Accepts healthy volunteers
No

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

  • Infertile married males diagnosed with clinical varicocele.
  • Age between 20-45 years.
  • Patients indicated for varicocelectomy according to standard clinical guidelines.
  • Abnormal or suboptimal semen parameters on at least two semen analyses.

Exclusion criteria

Exclusion Criteria:

  • Azoospermic patients (complete absence of sperm in semen).
  • History of previous varicocelectomy or scrotal surgery.
  • Presence of other known causes of infertility (e.g., genetic abnormalities, obstructive azoospermia).
  • Active genital infection or systemic infection affecting semen analysis.
  • Use of medications affecting spermatogenesis within the last 3 months (e.g., testosterone, chemotherapy).
  • Chronic systemic diseases known to affect fertility (e.g., uncontrolled diabetes, liver failure).
  • Severe leukocytospermia as confirmed by peroxidase (Endtz) test exceeding WHO reference limits.
  • Pus cell > 1 million/ml by peroxidase.
05

Study design

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

Study arms

  • Experimental
    Microsurgical Varicocelectomy

    Infertile married males aged 20-45 with clinical varicocele and abnormal semen parameters will form a single study arm. All participants will undergo a subinguinal microsurgical varicocelectomy. The surgical technique involves opening the spermatic fasciae under microscopic magnification (up to 10X), identifying and preserving the internal spermatic artery, and ligating the internal spermatic and cremasteric veins. Semen analysis, including spermatogenic cell quantification using combined morphological and enzymatic methods, will be conducted preoperatively and at 3 and 6 months postoperatively.

    Procedure: Subinguinal Microsurgical Varicocelectomy

Interventions

  • ProcedureSubinguinal Microsurgical Varicocelectomy

    A 3-4 cm subinguinal incision will be made below the external ring. Under 5-10X microscopic magnification, the internal spermatic artery will be identified and preserved. The internal spermatic veins and cremasteric veins, with the exception of vasal veins, will be ligated. The testicular arteries, cremasteric arteries, cremaster muscle fibers, nerves, lymphatic vessels, and vas deferens will be preserved before the spermatic cord is returned and the incision is closed.

06

What researchers measure

Primary outcomes

  1. Change in Seminal Spermatogenic Cell Count

    Spermatogenic cell concentration will be quantified using a Neubauer hemocytometer and expressed as x10⁶ cells/mL.

    Time frame: Preoperatively, and at 3 and 6 months postoperatively.

Secondary outcomes

  1. Change in Sperm Concentration

    The change in sperm concentration will be analyzed and measured in 10⁶/ml according to the World Health Organization (WHO) Laboratory Manual.

    Time frame: Preoperatively, and at 3 and 6 months postoperatively.

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07684963
Lead sponsor
Assiut University
Responsible party
Abdulkarim Mohammed Abdulkarim (Resident at Andrology and Sexology and STDs, Assiut University, Assiut University) — Principal investigator
First posted
Jul 6, 2026
Start date
Aug 2026 (estimated)
Primary completion
Aug 2027 (estimated)
Completion
Sep 2027 (estimated)
Last update
Jul 6, 2026

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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