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
| Type | Name | Description |
|---|---|---|
| DEVICE | Copper intrauterine contraceptive device | copper T-380 IUD |
| DEVICE | LNG-IUS | Levonorgestrel 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.