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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04694677
Other study ID # Myomectomy
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 10, 2021
Est. completion date September 10, 2021

Study information

Verified date January 2021
Source Aljazeera Hospital
Contact Mahmoud Alalfy
Phone 01002611058
Email mahmoudalalfy@ymail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Uterine leiomyomas (fibroids) are the most common benign tumors among women . Fibroids are found in approximately 15% to 30% of women in the reproductive age group


Description:

Although most of them are asymptomatic, 20-50% of fibroids may cause problems such as heavy menstrual bleeding, anemia, pelvic pain, pressure symptoms from extrinsic compression of the colorectal and urinary tract, infertility, and recurrent pregnancy losses, where surgical intervention is often indicated


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date September 10, 2021
Est. primary completion date August 15, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - women with myomas Exclusion Criteria: - with with malignant lesions

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
women receiving tranexamic acid
women receiving tranexamic acid during myomectomy
women receiving misoprostol
women receiving misoprostol in myomectomy

Locations

Country Name City State
Egypt Algazeerah Giza

Sponsors (2)

Lead Sponsor Collaborator
Aljazeera Hospital Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary the number of women who will have less blood loss how many women will have less blood loss 48 hours
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