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Sperm Retrieval Outcomes After Orchiopexy in Adult Patients with Bilateral Cryptorchidism and Nonobstructive Azoospermia: A Single-Center Retrospective Clinical Study

Sperm Retrieval Outcomes After Orchiopexy in Adult Patients with Bilateral Cryptorchidism and Nonobstructive Azoospermia: A Single-Center Retrospective Clinical Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129294
Enrollment
Unknown
Registered
2026-08-03
Start date
2026-08-14
Completion date
Unknown
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adult Patients with Bilateral Cryptorchidism and Non-obstructive Azoospermia

Interventions

Testicular fixation group:None

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Male, over 18 years old at the time of surgery or the first study of related diagnosis and treatment. 2. Previously diagnosed as bilateral cryptorchidism, and having not completed bilateral testicular descent treatment before seeking medical attention in adulthood. 3. Before the operation, the diagnosis of non-obstructive azoospermia was met, that is, no sperm was found in at least two semen analyses and centrifugation sediment tests, and a clear obstructive cause was ruled out in combination with clinical assessment. 4. During the period from March 1, 2005 to September 30, 2023, those who underwent surgical assessment, orchiopexy or related fertility preservation pathway management at Shanghai First People's Hospital. 5. Have a semen reexamination record or a postoperative micro-TESE record that can be used to determine the sperm acquisition after the operation.

Exclusion criteria

Exclusion criteria: 1. Only unilateral cryptorchidism, or the medical records cannot confirm bilateral lesions. 2. The main cause of the disease is obstructive azoospermia, or the existence of evaluable sperm acquisition before the operation makes it impossible to determine the postoperative outcome. 3. Key exposure variables or primary outcome data are missing and cannot be completed after medical record verification. 4. There are serious record conflicts, and after verification by the research team, the main diagnosis, surgery or outcome still cannot be confirmed. 5. Those whose previous medical records have been explicitly refused for scientific research analysis in their medical records or hospital records.

Design outcomes

Primary

MeasureTime frame
Postoperative fertility-usable sperm recovery;

Secondary

MeasureTime frame
The proportion and time of sperm detection in postoperative semen;The acquisition of micro-TESE sperm in patients with persistent azoospermia after surgery;The live birth outcome after using the obtained sperm;Testicular tumor events recorded in the medical records during the follow-up period;Changes in the status of biochemical hypogonadism before and after the operation;Changes in the status of biochemical hypogonadism before and after the operation;

Countries

China

Contacts

Public ContactLi Peng

Shanghai General Hospital

015123lp@shgh.cn+86 21 63240090

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 25, 2026