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Cavity Evaluation Before Intracytoplasmic Sperm Injection

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT04257708
Recruitment Status : Not yet recruiting
First Posted : February 6, 2020
Last Update Posted : February 6, 2020
Sponsor:
Information provided by (Responsible Party):
Aljazeera Hospital

Brief Summary:
Uterine cavity evaluation is an integral part of assessment Of women for ICSI

Condition or disease Intervention/treatment
Infertility Diagnostic Test: ultrasound

Detailed Description:
Transvaginal us is the main role in this aspect

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Study Type : Observational
Estimated Enrollment : 50 participants
Observational Model: Other
Time Perspective: Prospective
Official Title: Cavity Evaluation Before Intracytoplasmic Sperm Injection in Women With Infertility
Estimated Study Start Date : February 9, 2020
Estimated Primary Completion Date : November 10, 2020
Estimated Study Completion Date : January 10, 2021

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Infertility

Group/Cohort Intervention/treatment
normal uterine cavity Diagnostic Test: ultrasound
Transvaginal us to assess the cavity

abnormal uterine cavity Diagnostic Test: ultrasound
Transvaginal us to assess the cavity




Primary Outcome Measures :
  1. The number of women who will has positive pregnancy test [ Time Frame: within a year ]
    The women who will got pregnant



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years to 42 Years   (Adult)
Sexes Eligible for Study:   Female
Gender Based Eligibility:   Yes
Gender Eligibility Description:   Infertile women
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Women with infertility
Criteria

Inclusion Criteria:

  • women with infertility more than one year

Exclusion Criteria:

  • 2omen with medical disorders

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04257708


Contacts
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Contact: Mahmoud Alalfy 01002611058 mahmoudalalfy@ymail.com

Locations
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Egypt
Algazeerah
Giza, Egypt
Contact: Mahmoud Alalfy, master    +201002611058    mahmoudalalfy@ymail.com   
Contact: Ahmed Elgazzar, M.D    +201014005959      
Principal Investigator: Mahmoud Alalfy, master         
Sponsors and Collaborators
Aljazeera Hospital
Investigators
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Study Chair: Mahmoud Alalfy, PhD Algezeera

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Responsible Party: Aljazeera Hospital
ClinicalTrials.gov Identifier: NCT04257708    
Other Study ID Numbers: Uterus
First Posted: February 6, 2020    Key Record Dates
Last Update Posted: February 6, 2020
Last Verified: February 2020

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Infertility
Genital Diseases, Male
Genital Diseases, Female