Study About Patients Using Copper Intrauterine Device (IUD)
|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. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01541241|
Recruitment Status : Unknown
Verified February 2012 by Egymedicalpedia.
Recruitment status was: Recruiting
First Posted : February 29, 2012
Last Update Posted : February 29, 2012
|Condition or disease|
|Copper Intrauterine Device Induced Bleeding|
Show Detailed Description
|Study Type :||Observational|
|Estimated Enrollment :||100 participants|
|Observational Model:||Case Control|
|Official Title:||Uterine Haemodynamic Changes in Patients With Copper Intrauterine Device Induced Bleeding|
|Study Start Date :||January 2012|
|Actual Primary Completion Date :||January 2012|
|Estimated Study Completion Date :||May 2012|
copper IUD used
Group I: includes 50 cases using CIUD and complaining of menorrhagia or menometrorrhagia.
Group II: includes 50 cases using CIUD and not complaining of abnormal uterine bleeding.
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): NCT01541241
|Contact: Mohamed SE Elsafty, lecturer||01003922211 ext 002|
|Contact: Mohamed Elmandouh Mohamed, ass proff|
|Shoubra Maternity Hospital||Recruiting|
|Cairo, Shoubra, Egypt|
|Contact: Ayman Abdelazeem elgamal, Resident 010003385499 ext 002|
|Contact: Mohamed SE Elsafty, Lecture 01003922211 ext 002|
|Principal Investigator: Ayman Abdelazim Elgamal, resident|
|Principal Investigator:||Ayman Abdelazim Elgamal, Residant||Shoubra General Hospital|