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OpenTrials
Completed

NCT Number: NCT02158000

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

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

Completed

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Key information

Age range

23 year–48 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Benha univesity hospital

Banhā, El Qualyobia, 13518, Egypt

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • women with excessive endometrial fluid by transvaginal ultrasound during ICSI cycles

Exclusion criteria

  • none

Treatment and study plan

Group A

Other

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

Other names: Daflon

Primary outcomes

  1. the pregnancy rate

    Time frame: is checked 16 days after embryos transfer

    is assessed by :serum hCG test Beta sub-unit of hCG (serum hCG test)

Secondary outcomes

  1. presence of the fluid on the day of embryo transfer

    Time frame: at the day of embryo transfer

    detection of excessive endometrial fluid by transvaginal ultrasound during ICSI cycles

Sponsors and collaborators

Lead sponsor

Benha University

Other

Registry information

Important dates

Study start
2014
Primary completion
2021
Study completion
2021
First posted
Jun 6, 2014
Registry last updated
Jun 28, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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