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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04265495
Other study ID # AlBarakaBH-KAMAL
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 9, 2020
Est. completion date December 1, 2021

Study information

Verified date September 2021
Source Al Baraka Fertility Hospital
Contact Kamal eldin Rageh, M.D.
Phone 0097333153871
Email dr_kamal_rageh@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

a comparative study among dual trigger, urinary HCG and recombinant HCG regarding the outcome of ICSI- antagonist cycles


Description:

a comparative study among dual trigger, urinary HCG and recombinant HCG regarding the outcome (oocyte quality, fertilization rate, implantation rate, clinical pregnancy rate as well as the incidence of OHSS) in ICSI- antagonist cycles


Recruitment information / eligibility

Status Recruiting
Enrollment 600
Est. completion date December 1, 2021
Est. primary completion date November 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 22 Years to 40 Years
Eligibility Inclusion Criteria: - patients <40 years of age who underwent IVF/ICSI cycles using a GnRH antagonist protocol Exclusion Criteria: - age: > 40 years - BMI > 30 , - long agonist protocol - were chromosomal and genetic disorders, abnormal ultrasonogram of the uterine cavity

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Bahrain Al-BARAKA FERTILITY HOSPITAL Manama Adliya

Sponsors (1)

Lead Sponsor Collaborator
Al Baraka Fertility Hospital

Country where clinical trial is conducted

Bahrain, 

Outcome

Type Measure Description Time frame Safety issue
Primary clinical pregnancy rate, 4 WEEKS
Primary implantation rate, 2 WEEKS
Primary incidence of OHSS. 1 WEEK
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