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NCT02158000 Clinical Trial

Aspiration of Excessive Endometrial Fluid at the Day of Ovum Retrieval Plus Diosmin in (ICSI) Cycles

Infertility Clinical Trial

Official title:
Aspiration of Excessive Endometrial Fluid at the Day of Ovum Retrieval Plus Diosmin in (ICSI) Cycles

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02158000
Other study ID # khalid-ahmed 5
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 2014
Est. completion date November 2021

Study information
Verified date June 2022
Source Benha University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To notify the effect of aspiration of excessive endometrial fluid in addition to Diosmin in cases undergoing intracytoplasmic sperm injection (ICSI) cycles.

Description:

Objectives: To notify the effect of aspiration of excessive endometrial fluid in addition to Diosmin in cases undergoing intracytoplasmic sperm injection (ICSI) cycles. Study design: Prospective randomized controlled clinical trial. Patients and Methods: 200 women with excessive endometrial fluid by transvaginal ultrasound during ICSI cycles are randomly scheduled into two equal groups. In group A, one tab every 8 hs Diosmin ( 500mg) beginning from the day of ovum retrieval in addition to aspiration of the fluid by an IUI catheter ; while in group B (control group), no thing is given or done. The main outcome measures are presence of the fluid on the day of embryo transfer and the pregnancy rate on those patients.

Recruitment information / eligibility
Status Completed
Enrollment 200
Est. completion date November 2021
Est. primary completion date November 2021
Accepts healthy volunteers No
Gender Female
Age group 23 Years to 48 Years
Eligibility Inclusion Criteria: - women with excessive endometrial fluid by transvaginal ultrasound during ICSI cycles Exclusion Criteria: - none

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• group A
one tab every 8 hs Diosmin ( 500mg) beginning from the day of ovum retrieval in addition to aspiration of the fluid by an IUI catheter

Locations
Country Name City State
Egypt Benha univesity hospital Banha El Qualyobia

Sponsors (1)
Lead Sponsor Collaborator
Benha University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary the pregnancy rate is assessed by :serum hCG test Beta sub-unit of hCG (serum hCG test) is checked 16 days after embryos transfer
Secondary presence of the fluid on the day of embryo transfer detection of excessive endometrial fluid by transvaginal ultrasound during ICSI cycles at the day of embryo transfer
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