NCT Number: NCT03153436
The Effect of In-vitro Myoinositol Supplementation of Human Sperm on the Outcome of Cryopreservation
The objective of this study is to evaluate the effect of in-vitro myoinositol supplementation of human sperm on the outcome of cryopreservation.
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Notify MeKey information
Conditions
Age range
20 year–60 year
Sex eligibility
Male
Study type
Interventional
Phase
Phase 1 / Phase 2
About this study
Sperm cryopreservation is considered the most valuable and used way to preserve male reproductive function. Unfortunately, osmotic effects of freezing and thawing during the cryopreservation process negatively affect sperm morphology and motility .
Myoinositol is the most biologically important form of inositol in nature. In male reproductive system, myoinositol appears to regulate sperm motility, capacitation and acrosomal reaction.
The objective of this study is to evaluate the effect of in-vitro myoinositol supplementation of human sperm on the outcome of cryopreservation.
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Infertile men with normal or abnormal semen analysis
Exclusion criteria
- Azoospermic samples
Treatment and study plan
Primary outcomes
-
Cryo-survival rate
Time frame: 7 months
Post-thawing cryo-survival rates of both aliquots ( myo and control) are compared in both groups (A and B).
Sponsors and collaborators
Lead sponsor
Sohag University
Other
Collaborators
- Ajyal Hospital
Registry information
Important dates
- Study start
- 2016
- Primary completion
- 2017
- Study completion
- 2017
- First posted
- May 15, 2017
- Registry last updated
- May 16, 2017
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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