Clinical Trials Directory

Trials / Unknown

UnknownNCT05986344

Uterine Artery Doppler and Menstrual Changes After Insertion Intrauterine Contraceptive Device

Correlation Between Uterine Artery Doppler Indices and Menstrual Changes After Insertion of Copper Intrauterine Contraceptive Device and Levonorgestrel Intrauterine System

Status
Unknown
Phase
Study type
Observational
Enrollment
165 (estimated)
Sponsor
Beni-Suef University · Academic / Other
Sex
Female
Age
20 Years – 40 Years
Healthy volunteers
Accepted

Summary

To evaluate the correlation between uterine artery Doppler indices and subsequent menstrual changes after 3 months of insertion of copper T-380 IUD and LNG-IUS

Detailed description

A randomized prospective clinical trial Study Population: The study population includes multiparous women, having normal menstrual cycles, who are eligible for insertion of IUCD. Women will be recruited for enrollment when they come to the family planning clinic. They will be counseled about different contraceptive options. If they want to have the IUCD, they will be asked to participate in the study after been evaluated to ensure fulfilling inclusion and exclusion criteria Women will be enrolled in the study after giving written informed consent Group (A): ….Women will have the copper T-380 IUD (PREGNA, India, imported by DKT Egypt LLC-Egypt) ® IUD. Group (B): …. Women will recieve the LNG-IUS (Mirena, Bayer HealthCare, Berlin, Germany)® IUD .

Conditions

Interventions

TypeNameDescription
DEVICECopper intrauterine contraceptive devicecopper T-380 IUD
DEVICELNG-IUSLevonorgestrel Intrauterine System

Timeline

Start date
2023-08-30
Primary completion
2023-12-30
Completion
2023-12-30
First posted
2023-08-14
Last updated
2023-08-15

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT05986344. Inclusion in this directory is not an endorsement.