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Male Infertility and Assisted Reproductive Technologies Research Biobank (MARK)

R

Reproductive Medicine Associates of New Jersey

Status

Enrolling

Conditions

Male Infertility
Infertility (IVF Patients)

Study type

Observational

Funder types

Other

Identifiers

NCT06880302
RMA-2022-01

Details and patient eligibility

About

The objective of this research is to build a biobank of biological male specimens used for diagnostics and treatment of infertility or assisted reproductive technologies (ART).

Full description

The objective of this research is to build a biobank of biological male specimens used for diagnostics and treatment of infertility or assisted reproductive technologies (ART). These specimens include testicular tissue, sperm, semen samples, donor sperm or discarded sperm preps. These samples were possibly utilized for diagnostic testing such as semen analyses or DNA fragmentation testing or for ART procedures such as intrauterine insemination (IUI) in-vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) and are no longer needed clinically. Rather than discarding those samples the men who provided them or the sperm recipient in the case of donor sperm may elect to donate them for future research purposes. These samples will be used for future research regarding male infertility and assisted reproductive technologies.

Enrollment

1,000 estimated patients

Sex

Male

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Males providing testicular tissue, sperm, semen samples, discarded sperm preps for IUI/IVF/ICSI or the sperm recipient for those utilizing donor sperm, for cryopreservation at the respective site(s) for either clinical use or preservation

Exclusion criteria

  • Samples that are quarantined or in isolation dewars for infectious diseases

Trial design

1,000 participants in 1 patient group

Males providing specimen for infertility treatment
Description:
Males providing specimen for infertility treatment

Trial contacts and locations

1

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Central trial contact

Christine Whitehead, MS, BSN, RN; Caroline Zuckerman, RN BSN

Data sourced from clinicaltrials.gov

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