Experimental Round Spermatid Injection (ROSI) to Treat Infertile Couples

Sponsor
Wake Forest University Health Sciences (Other)
Overall Status
Recruiting
CT.gov ID
NCT04298255
Collaborator
Carolinas Fertility Institute (CFI) (Other), Wake Forest Institute for Regenerative Medicine (WFIRM) (Other), Wake Forest Department of Urology (Other)
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Study Details

Study Description

Brief Summary

The purpose of this research study is to evaluate if special types of cells called round spermatids can be gathered from men with non-obstructive azoospermia and used (in absence of elongated spermatids and spermatozoa) to reliably and effectively create pregnancy with a procedure called Round Spermatid Injection (ROSI). This process is similar to In Vitro Fertilization, or 'IVF'. In addition, this study wants to test the safety of ROSI and see what effects (good and bad) it has on embryo created from this method.

Condition or Disease Intervention/Treatment Phase
  • Other: Round Spermatid Injection (ROSI)
  • Other: Half ROSI-half Sperm Donor Fertilization
N/A

Detailed Description

Azoospermia is defined as the absence of sperm in the ejaculate. Around 1% of general population suffers from azoospermia. Men who were rendered infertile due to a non-obstructive azoospermia, who have been subjected to Testicular Sperm Extraction (TESE) surgery and found to be lacking elongated spermatids or spermatozoa, are commonly advised to consider utilizing a sperm donor or apply for adoption. It is reported that ~30% of men with non-obstructive azoospermia lack elongated spermatids and spermatozoa but may still produce round spermatids (less mature form of haploid germ cells) in their testicles. Round Spermatid Injection (ROSI) technology to fertilize oocytes is not a brand-new technology, however, it is plagued with notoriously low efficiency. Despite this limitation, it has been reported that most of these patients still desire to have the ROSI procedure instead of applying directly for other options, i.e. sperm donation or adoption.

High failure rate of traditional ROSI has been attributed to a few potential causes:
  1. Incorrect selection of round spermatids (to distinguish from diploid spermatogonia cells)

  2. Using round spermatids that were already in the process of degeneration

  3. Incomplete imprinting in the round spermatid

  4. Incomplete activation of oocytes Recently Tanaka and colleagues in Japan established a new ROSI method and reported over 90 babies born via this method1. They described a new method of round spermatid selection and oocyte activation using NEPA21 super electroporator (10 minutes prior to round spermatid injection).

Babies born from this new ROSI method in Japan have been evaluated for developmental and cognitive differences for 2 years1. Babies conceived with ROSI were found to have a shorter gestation times, and lower body weight at 12 and 18 months when compared to their naturally conceived counterparts, but also showed an increased birth weight and showed no body weight differences at 24 months of age. No diseases resulting from genetic anomalies have been reported thus far, but the relatively small sample sizes present in the literature needs to be tested in larger cohorts. Therefore, this effective ROSI method should still be considered as an "experimental fertility treatment".

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Intervention Model Description:
Infertile Male with round spermatid (but not elongated spermatids and spermatozoa) in their testes. Couples can choose either option 1 or 2.Infertile Male with round spermatid (but not elongated spermatids and spermatozoa) in their testes. Couples can choose either option 1 or 2.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Experimental Round Spermatid Injection (ROSI) to Treat Infertile Couples
Actual Study Start Date :
Aug 24, 2020
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: ROSI only

Option 1: injecting extracted round spermatids (less mature form of haploid germ cells than elongated spermatid or spermatozoon) from male partner into the harvested egg of a female partner

Other: Round Spermatid Injection (ROSI)
In Vitro Fertilization using Round Spermatid Injection (ROSI)

Experimental: Half ROSI-half Sperm Donor Fertilization

Option 2: Harvested eggs from the female partner will be separated in two groups, with one group being fertilized with round spermatids and the other group fertilized with donor sperm

Other: Half ROSI-half Sperm Donor Fertilization
Half ROSI-half Sperm Donor Fertilization

Outcome Measures

Primary Outcome Measures

  1. Fertility rate [Day 1 after round spermatid injection]

    Egg fertilization comparison between the groups undergoing the procedure with spermatids only vs spermatids and donor sperms.This fertilization process will be recorded by EmbryoScope under supervision of dedicated clinical embryologist.All the process will be followed and documented according to America Society of Reproductive Medicine (ASRM) guidelines. All the process will be followed and documented according to American Society for Reproductive Medicine (ASRM) guidelines.

Secondary Outcome Measures

  1. Blastocyst formation [Day 3 to 5 after round spermatid injection]

    Blastocyst comparison between the groups undergoing the procedure with spermatids only vs spermatids and donor sperms.Embryo grow and blastocyst formation will be recorded by EmbryoScope under supervision of dedicated clinical embryologist.All the process will be followed and documented according to American Society for Reproductive Medicine (ASRM) guidelines.

  2. Aneuploidy rate [Day 3 to 5 after round spermatid injection]

    Aneuploidy comparison and evaluation of abnormality between the groups undergoing the procedure with spermatids only vs spermatids and donor sperms. Aneuploidy will be tested using polymerase chain reaction amplification (PCR) based Preimplantation genetic diagnosis (PGD) and fluorescent in situ hybridization (FISH) analyses. All the process will be followed and documented according to American Society for Reproductive Medicine (ASRM) guidelines.

  3. Chemical Pregnancy with Positive human chorionic gonadotropin (hCG) [Post Fertilization 4 Weeks and onwards]

    Pregnancy Rate between the groups undergoing the procedure with spermatids only vs spermatids and donor sperms. Blood test to measure beta-hCG (chemical pregnancy) and follows by Ultrasound (clinical pregnancy). All the process will be followed and documented according to American Society for Reproductive Medicine (ASRM) guidelines.

  4. Live Birth Rate [Post Pregnancy Full Term Average 39 to 40 weeks]

    Live Birth comparison between the groups undergoing the procedure with spermatids only vs spermatids and donor sperms. Pregnancy will be followed as high risk and health of born children will be evaluated by a dedicated neonatologist/Pediatrician. All the process will be followed and documented according to American Society for Reproductive Medicine (ASRM) guidelines.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Males with no elongated spermatids or spermatozoa present but with round spermatids present on TESE (Testicular Sperm Extraction)

  • Male diagnosed with non-obstructive Azoospermia

  • Male partner ≥18

  • Female partner greater than 18 years of age and less than 38 years of age or Anti Mullerian Hormone (AMH) greater than 2 ng/ml.

Exclusion Criteria:
  • Males with obstructive azoospermia

  • Males with presence an adequate number of elongated spermatids or spermatozoa

Contacts and Locations

Locations

Site City State Country Postal Code
1 Carolinas Fertility Institute (CFI) Winston-Salem North Carolina United States 27103

Sponsors and Collaborators

  • Wake Forest University Health Sciences
  • Carolinas Fertility Institute (CFI)
  • Wake Forest Institute for Regenerative Medicine (WFIRM)
  • Wake Forest Department of Urology

Investigators

  • Principal Investigator: Hooman Sadri, MD, PhD, Wake Forest Institute for Regenerative Medicine (WFIRM)
  • Study Director: Hooman Sadri, MD, PhD, Wake Forest University Health Sciences

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Wake Forest University Health Sciences
ClinicalTrials.gov Identifier:
NCT04298255
Other Study ID Numbers:
  • IRB00062898
First Posted:
Mar 6, 2020
Last Update Posted:
Dec 29, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Wake Forest University Health Sciences
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 29, 2021