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Compares treatment options for Bilateral Varicocele
Official title Single Infrapubic Versus Bilateral Subinguinal Microsurgical Varicocelectomy
ClinicalTrials.gov ID: NCT07650955
What this study is testing
- What it's testing
- Bilateral varicocele is commonly treated by microsurgical varicocelectomy. The conventional bilateral subinguinal approach usually requires two separate skin incisions, one on each side.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 45, men only
You may be able to join if
- Male patients aged 18 to 45 years.
- Clinically palpable bilateral varicocele, grade II or grade III.
- Diagnosis confirmed by color Doppler ultrasound.
- Infertility for at least 12 months and/or abnormal semen analysis.
- Female partner evaluation performed or planned to exclude major uncorrected female-factor infertility.
You likely can't join if
- Subclinical varicocele detected only by Doppler ultrasound.
- Unilateral varicocele.
- Recurrent varicocele after previous surgery, embolization, or sclerotherapy.
- Previous inguinal, scrotal, pelvic, or penile surgery likely to distort surgical anatomy.
- Associated inguinal hernia, hydrocele, spermatocele, epididymal cyst, or other scrotal condition requiring simultaneous surgery.
- Azoospermia, especially suspected non-obstructive azoospermia.
See the full eligibility criteria
- Male patients aged 18 to 45 years.
- Clinically palpable bilateral varicocele, grade II or grade III.
- Diagnosis confirmed by color Doppler ultrasound.
- Infertility for at least 12 months and/or abnormal semen analysis.
- Female partner evaluation performed or planned to exclude major uncorrected female-factor infertility.
- Patient fit for surgery and anesthesia.
- Written informed consent provided by the participant.
- Subclinical varicocele detected only by Doppler ultrasound.
- Unilateral varicocele.
- Recurrent varicocele after previous surgery, embolization, or sclerotherapy.
- Previous inguinal, scrotal, pelvic, or penile surgery likely to distort surgical anatomy.
- Associated inguinal hernia, hydrocele, spermatocele, epididymal cyst, or other scrotal condition requiring simultaneous surgery.
- Azoospermia, especially suspected non-obstructive azoospermia.
- Active urinary tract or genital infection.
- Coagulopathy or anticoagulant therapy that cannot be safely interrupted.
- Severe obesity, defined as body mass index greater than 40 kg/m², or any anatomical condition preventing safe exposure by either surgical approach.
- Refusal to participate or inability to complete follow-up.
The study team makes the final eligibility decision.
Where it's taking place
- Banī Suwayf, Beni Suweif Governorate, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling male, 18 years to 45 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Banī Suwayf, Beni Suweif Governorate, Egypt. Enter your location above to see the nearest site and check your eligibility.
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BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.