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New treatment option for IUCD Complication
Official title Clinical and Ultrasonographic Predictors of IUD Related Complications
ClinicalTrials.gov ID: NCT06806358
What this study is testing
- What it's testing
- All patients fulfilling the selection criteria undergo complete clinical examination and detailed medical history obtained. Each patient had a Case Record Form (CRF) recording participants' name.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 20 to 41, women only
You may be able to join if
- Age 20 -41 years
- BMI 18-25 kg/m2
- Women with any parity seeking contraception and choosing IUD as their preferred method after proper and thorough counseling
- Regularly menstruating women (duration of menstruation 3-7 days and length of cycle 22- 35 days).
- Not using any hormonal therapy or anticoagulation
You likely can't join if
- Cervical abnormalities.
- Pregnancy or suspicion of pregnancy
- Congenital or acquired uterine anomalies which distort the uterine cavity (fibroids, endometrial polyps, cervical stenosis, bicornuate uterus...
- Acute PID or a history of PID within the past 3 months
- Postpartum or post-abortion endometritis within the past 3 months
- Current STI or within the past 3 months (including cervicitis)
See the full eligibility criteria
- Age 20 -41 years
- BMI 18-25 kg/m2
- Women with any parity seeking contraception and choosing IUD as their preferred method after proper and thorough counseling
- Regularly menstruating women (duration of menstruation 3-7 days and length of cycle 22- 35 days).
- Not using any hormonal therapy or anticoagulation
- Cervical abnormalities.
- Pregnancy or suspicion of pregnancy
- Congenital or acquired uterine anomalies which distort the uterine cavity (fibroids, endometrial polyps, cervical stenosis, bicornuate uterus, hypoplastic uterus \< 6 cm)
- Acute PID or a history of PID within the past 3 months
- Postpartum or post-abortion endometritis within the past 3 months
- Current STI or within the past 3 months (including cervicitis)
- Cervical cancer
- Endometrial cancer
- Malignant gestational trophoblastic disease
- Undiagnosed vaginal bleeding
- Hypersensitivity to any component in the IUD (copper)
- Less than 6 weeks postpartum.
- Neurological or psychological conditions that may affect pain sensation
The study team makes the final eligibility decision.
Where it's taking place
- Cairo, Egypt
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 20 years to 41 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Cairo, Egypt. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.