5★ on Google · 450+ reviews MCh AIIMS Delhi · FRCS Oxford University, England Apollo Hospital Gurugram + Six Sigma Clinics NEW +91 78382 86336

Nil Sperm Count · Gurgaon

Azoospermia Treatment in Gurgaon

Being told there are no sperm does not mean there is no hope. Azoospermia has two distinct causes - and treatment differs entirely. Dr. Nitin Shrivastava identifies which type you have before recommending any intervention. MCh AIIMS Delhi · FRCS Oxford.

Book confidential consultation Male infertility overview

"No sperm in the ejaculate" does not mean "no sperm in the body." In obstructive azoospermia, sperm production is completely normal - the blockage just prevents them from appearing in the ejaculate. In non-obstructive azoospermia, small islands of sperm production may still be present in the testicle, retrievable with MicroTESE. The correct diagnosis determines the correct treatment.

Diagnosis first

Two types of azoospermia - completely different treatments

Obstructive Azoospermia (OA)

Sperm are produced normally but cannot exit due to a blockage in the epididymis, vas deferens, or ejaculatory ducts.

FSH:Normal
Testes:Normal size and consistency
Causes:Vasectomy, epididymal blockage (post-infection), congenital absence of vas deferens (CBAVD), ejaculatory duct obstruction
Treatment:Vasectomy reversal, PESA/TESA, surgical reconstruction
Prognosis:Excellent - high sperm retrieval rates

Non-Obstructive Azoospermia (NOA)

Sperm production itself is impaired - due to testicular failure, chromosomal causes, or hormonal problems.

FSH:Often elevated (compensatory rise)
Testes:May be small or softer
Causes:Klinefelter syndrome (47,XXY), Y-microdeletion, chemotherapy, idiopathic, hormonal failure
Treatment:MicroTESE (micro-dissection TESE) - finds sperm in 40–60% of men
Prognosis:MicroTESE retrieves sperm in 40–60%

Investigations

Complete workup before any treatment

1
Two semen analysesBoth must be examined after centrifugation of the ejaculate. A single analysis is not sufficient to diagnose azoospermia. Abstinence of 3–5 days before each test. Performed at an andrology-certified laboratory.
2
Hormonal profileFSH, LH, total testosterone, prolactin, inhibin B. Elevated FSH + low inhibin B = poor spermatogenesis (NOA). Normal FSH with normal testes = likely OA. Low FSH + low testosterone = hypogonadotrophic hypogonadism (treatable hormonally - sperm may appear without surgery).
3
Karyotype (chromosomal analysis)Identifies Klinefelter syndrome (47,XXY) - the most common chromosomal cause of NOA. Found in approximately 10–14% of NOA patients. Important before MicroTESE as it affects counselling and success rate estimation.
4
Y-chromosome microdeletion testingAZFa or AZFb deletions: MicroTESE is unlikely to retrieve sperm - couple should be counselled that donor sperm may be the path. AZFc deletion: sperm may still be present at MicroTESE (50% success rate). This blood test is mandatory before performing MicroTESE in NOA.
5
Scrotal ultrasound + transrectal ultrasoundAssesses testicular volume (atrophy suggests NOA), epididymal dilation (OA), presence of vas deferens, and ejaculatory duct cysts or calcifications (ejaculatory duct obstruction - treatable by TUIED).
6
Genetic counsellingFor chromosomal causes, Y-microdeletions, or CBAVD (associated with CFTR mutations) - genetic counselling of the couple before proceeding to sperm retrieval and IVF is strongly recommended.

Treatment options

Matched to your specific diagnosis

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Vasectomy reversal

For post-vasectomy OA - microsurgical vasovasostomy or epididymovasostomy. Restores natural fertility without IVF if done within 10–15 years. See vasectomy reversal page.

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PESA / TESA

Percutaneous epididymal or testicular sperm aspiration for OA. Simple outpatient procedure with local/sedation anaesthesia. Sperm combined with partner's eggs via IVF-ICSI.

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MicroTESE

Microdissection testicular sperm extraction for NOA. Operating microscope identifies viable tubules. 40–60% sperm retrieval rate. Dr. Nitin's technique of choice for NOA.

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Hormonal therapy

For hypogonadotrophic hypogonadism: gonadotropin injections (FSH + hCG) stimulate sperm production. Sperm may appear in ejaculate after 3–12 months - IVF may not be needed.

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TUIED

Transurethral incision of ejaculatory ducts - for ejaculatory duct obstruction (cysts or calcifications). Outpatient endoscopic procedure. Sperm return to ejaculate.

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Donor sperm

For AZFa/AZFb deletion or failed MicroTESE - when biological fatherhood is not possible. Counselled compassionately as part of the complete fertility discussion.

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Been told nothing can be done?

Many men with azoospermia are told their only option is donor sperm - before a proper diagnostic workup. MicroTESE retrieves sperm in 40–60% of NOA cases, including men with Klinefelter syndrome and some Y-microdeletion patterns. International guidelines recommend MicroTESE before excluding biological fatherhood. A complete workup (karyotype, Y-microdeletion, hormones) takes 2–3 weeks. That is all the time needed to know whether MicroTESE is worth attempting.

Get a proper workup first →

Why Dr. Nitin?

Training
MCh Urology - AIIMS Delhi · FRCS Urology - Oxford University
Technique
MicroTESE with operating microscope · Microsurgical vasectomy reversal · PESA/TESA
Approach
Complete workup before surgery · Couple-centred · IVF centre coordination
Location
Apollo Hospital Gurugram · Six Sigma Clinics, Sector 50

Video Education

Watch Dr. Nitin on Azoospermia

Zero sperm count explained - causes, tests, and treatment options

Azoospermia: Zero Sperm Count Treatment – Dr. Nitin Shrivastava

Azoospermia: Zero Sperm Count Treatment

Male Infertility & Sperm Retrieval – Dr. Nitin Shrivastava

Male Infertility & Sperm Retrieval

Frequently asked questions

Azoospermia - your questions answered

Azoospermia means no sperm are detected in the ejaculate on two separate semen analyses. It affects approximately 1% of all men and 10–15% of men presenting with infertility. It does not always mean no sperm exist in the body. Obstructive azoospermia (OA) - where sperm are produced but blocked - has excellent treatment outcomes. Non-obstructive azoospermia (NOA) - where sperm production is impaired - can still yield sperm in 40–60% of cases using MicroTESE. The key is accurate diagnosis before assuming nothing can be done.

Obstructive azoospermia (OA): sperm production is normal but outflow is blocked - due to vasectomy, epididymal blockage (post-infection), absent vas deferens (CBAVD), or ejaculatory duct obstruction. FSH is typically normal, testicular size is normal, and sperm can be retrieved by PESA or TESA. Pregnancy rates with IVF-ICSI using retrieved sperm are excellent. Non-obstructive azoospermia (NOA): sperm production itself is impaired - due to Klinefelter syndrome (47,XXY), Y-chromosome microdeletions, hormonal failure, chemotherapy, or idiopathic causes. FSH is often elevated, testes may be small. MicroTESE can retrieve sperm in 40–60% of cases.

MicroTESE (microdissection TESE) uses an operating microscope to examine the testicular tissue directly and identify dilated seminiferous tubules - the ones more likely to contain sperm - rather than taking random biopsy cores. This approach retrieves more sperm, removes far less testicular tissue, and causes significantly less post-operative testosterone decline than conventional TESE. Success rates for NOA are 40–60% with MicroTESE versus 16–45% with conventional TESE. For men with NOA, MicroTESE is the internationally recommended approach and Dr. Nitin's preferred technique.

A complete workup includes: two semen analyses (both must show zero sperm on centrifuged sample). Hormones: FSH, LH, testosterone, prolactin, inhibin B - these distinguish OA from NOA. Karyotype (chromosomal analysis): to detect Klinefelter syndrome (47,XXY) or other chromosomal abnormalities. Y-chromosome microdeletion analysis: AZFa, AZFb deletions predict no sperm will be found at MicroTESE (AZFa or AZFb deletion = MicroTESE not recommended). AZFc deletion: partial sperm production may still be present. Scrotal and transrectal ultrasound: assess testicular volume, detect ejaculatory duct obstruction or absent vas. Testicular biopsy: only if needed to confirm maturation arrest or Sertoli-cell-only syndrome.

Hormonal treatment is beneficial in specific cases: hypogonadotrophic hypogonadism (low FSH and LH causing low testosterone) responds dramatically to gonadotropin injections - sperm may appear in the ejaculate after 3–12 months of treatment, avoiding the need for surgical sperm retrieval. This is a reversible, treatable cause that must not be missed. Post-chemotherapy or radiation-induced azoospermia occasionally recovers spontaneously or with hormonal support - semen analysis should be repeated at 12 and 24 months before considering sperm retrieval surgery. Idiopathic NOA does not reliably respond to empirical hormone treatment; MicroTESE is the primary option.

Sperm retrieved at MicroTESE can be used fresh for same-day IVF-ICSI (intracytoplasmic sperm injection) with your partner's eggs, or cryopreserved (frozen) for future IVF cycles. Cryopreservation is often preferred as it allows the female partner's ovarian stimulation to be optimised separately. IVF-ICSI success rates using testicular sperm depend on female partner age and ovarian reserve, sperm quality retrieved, and the fertility centre's laboratory capabilities. Dr. Nitin coordinates closely with IVF centres for optimal timing and sperm handling.

Yes - in approximately 40–50% of cases. Klinefelter syndrome (47,XXY) is the most common chromosomal cause of male infertility and azoospermia, but focal areas of sperm production may persist in the testicle. MicroTESE can retrieve sperm in approximately 40–50% of Klinefelter men, particularly before age 35 and when testosterone levels have been optimised. The retrieved sperm are used for IVF-ICSI. Genetic counselling is recommended beforehand, as there is a small increased risk of sex chromosome abnormalities in offspring (though preimplantation genetic testing can screen for this).

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