NCT Number: NCT02424214
Artificial Oocyte Activation Comparing Tow Different Agents
Comparing the efficacy of tow factors for artificial Oocyte Activation for poor quality Oocytes and Teratozoospermia patients.
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Notify MeKey information
Conditions
Age range
18 year–40 year
Sex eligibility
Female
Study type
Interventional
Phase
Not applicable
Primary location
Al Barka fertility center, Manama, Bahrain
About this study
The IVF outcome had been varied widely with a good portion of total fertilization failure even after the most advanced procedure for this group of patient Intracytoplasmic Sperm Injection, many factors that had been tested for assisting the failed group of patient to be fertilized artificially like Ca Ionophore, Strontium Chloride and others but we decide to compare the clinically proven factors for the efficacy and safety in a well randomized clinical trial and monitor the embryogenesis and pregnancy within the 2 groups.
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- previous fertilization failure
- poor quality Oocytes
- poor sperms
Exclusion criteria
- normal patients
Treatment and study plan
Ca Ionophore
DrugStrontium Chloride
DrugPrimary outcomes
-
Pregnancy rate ( % )
Time frame: 9 months
Secondary outcomes
-
Blastocyst rate ( % )
Time frame: 9 months
Sponsors and collaborators
Lead sponsor
Ibn Sina Hospital
Other Gov
Collaborators
- Al Baraka Fertility Hospital
- Banon IVF Center Assiut, Egypt
Registry information
Important dates
- Study start
- 2015
- Primary completion
- 2016
- Study completion
- 2016
- First posted
- Apr 22, 2015
- Registry last updated
- Feb 19, 2018
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.