Oxidative Stress in Testicular Tissue Before and After Cryopreservation

NCT ID: NCT03621995

Last Updated: 2019-07-16

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 58 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2018-09-10
• Study Completion Date: 2018-11-30

Brief Summary

The absence of sperms in ejaculated semen, is the most severe form of male-factor infertility and is present in approximately 5 % of all investigated infertile couples.

Detailed Description

Obstructive azoospermia is defined as the absence of spermatozoa in the ejaculate despite normal spermatogenesis.Infection, Iatrogenic injury, Vasectomy and congenital atresia are the possible causes of it. Non obstructive or functional azoospermia results from testicular failure, which is the absence or inadequate production of fully developed spermatozoa within the testes.

Etiologies for testicular failure include genetic disorders such as sexual chromosomal abnormalities ; translocations and microdeletions of the Y chromosome; cryptorchidism; testicular torsion; radiation and toxins.

The advent of intra-cytoplasmic sperm injection has transformed the treatment of this type of severe male-factor infertility.

Surgical techniques for sperm retrieval:Testicular sperm aspiration: In men with obstructive azoospermia ,testicular sperm aspiration invariably generates enough sperm for intra-cytoplasmic sperm injection.

Testicular sperm extraction:This conventional method of surgical sperm extraction generally offers the best chance of retrieving spermatozoa, especially in functional cases and when guided by surgical microscope. However, it can be done by simple open conventional biopsy and closed surgical extraction resembling Trucut biopsy using a special cannula.

Cryopreservation Cryopreservation of human testicular tissue obtained by biopsy can be used as a potential future source of sperms. For adult cancer survivors, cryopreservation of testis biopsies may be the only option remaining if they prefer to father their own biological progeny.

There are 4 types of cryopreservation :

Slow freezing: involves step-wise programmed decrease in temperature. Rapid freezing: was first proposed by . Ultra-rapid freezing :can be considered midway technique between slow freezing and vitrification.

Vitrification: solidifies the sample into a glass-like state. During the freezing process,increasing in susceptibility of spermatozoa to lipid peroxidation,as affected by cold shock, plays an important role in ageing of spermatozoa ,shortening their lifespan and affecting the preservation of semen.The major susceptibility is related in, part to the content of polyunsaturated fatty acids.

Oxidative stress and antioxidants: Oxygen is required to support life, but its metabolites, such as reactive oxygen species, can modify cell functions and endanger cell survival. For this reason,reactive oxygen species is inactivated continuously to maintain only the small amount necessary to maintain normal cell function. There is a balance between the different antioxidants and oxidants at normal status. Oxidative stress is a cellular condition associated with an imbalance between the production of free radicals, mainly reactive oxygen species, and the scavenging capacity of antioxidants.

Superoxide dismutase and catalase are endogenous antioxidants, which protect cells from oxidative stress. Scavengers of reactive oxygen species and antioxidants are important in treating and preventing the damage caused by such stress.

Catalase has been reported from testis, seminal plasma, and spermatozoa Tissue level of malondialdehyde is proven indicator of oxidative stress resulting from lipid peroxidation .

The process of cryopreservation is known to cause more production and/or accumulation of reactive oxygen species, as antioxidant defenses are reduced in the process.

Conditions

Oxidative Stress

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: RETROSPECTIVE

Study Groups

Obstructive azoospermia

Malondialdehyde and Catalase level measurement before and after cryopreservation

Malondialdehyde and Catalase level measurement

Intervention Type: OTHER

Malondialdehyde and Catalase level measurement by colorimetric method

Non obstructive azoospermia

Malondialdehyde and Catalase level measurement before and after cryopreservation

Malondialdehyde and Catalase level measurement

Intervention Type: OTHER

Malondialdehyde and Catalase level measurement by colorimetric method

Negative group

Malondialdehyde and Catalase level measurement without cryopreservation

Malondialdehyde and Catalase level measurement

Intervention Type: OTHER

Malondialdehyde and Catalase level measurement by colorimetric method

Interventions

Malondialdehyde and Catalase level measurement

Malondialdehyde and Catalase level measurement by colorimetric method

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Men with azoospermia at reproductive age .

Exclusion Criteria

• Pyospermia.
• Previous trial of cryopreservation.
• Systemic diseases.
• Cryptorchidism history.
• Smoking

• Minimum Eligible Age: 14 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

Assiut University

OTHER

Sponsor Role: lead

Responsible Party

Aya Hasan

Resident in dermatology department

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Aya H Younis, Resident

Role: PRINCIPAL_INVESTIGATOR

Assiut University

Locations

Assuit University Hospital

Asyut, , Egypt

Countries

Egypt

Other Identifiers

OSITTBAAC

Identifier Type: -

Identifier Source: org_study_id