Actively Recruiting
Clinical and Ultrasonographic Predictors of IUD Related Complications
Led by Cairo University · Updated on 2025-03-18
200
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
* 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. number, previous deliveries and abortions, age, height, weight, BMI, LMP, past medical and surgical history and contraceptive history. * All participants will be subjected to transvaginal ultrasound to measure uterine size, endometrial and myometrial thickness, uterine position, cervical length, cervical diameter and for detection of any contraindications for IUD insertion. Power Doppler Energy (PDE) measurement for subendometrial microvascularization will be done and categorized as women with minor subendometrial vascularization (Classifications I and II) and major subendometrial vascularization (Classifications III, IV and V)
CONDITIONS
Official Title
Clinical and Ultrasonographic Predictors of IUD Related Complications
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 20 - 41 years
- BMI 18-25 kg/m2
- Women with any number of previous births seeking contraception and choosing IUD after counseling
- Regular menstrual cycles lasting 3-7 days and occurring every 22-35 days
- Not currently using hormonal therapy or blood thinners
You will not qualify if you...
- Cervical abnormalities
- Pregnancy or suspicion of pregnancy
- Uterine anomalies that change the shape of the uterine cavity (including fibroids, polyps, cervical stenosis, bicornuate or underdeveloped uterus less than 6 cm)
- Acute pelvic inflammatory disease or history of PID within past 3 months
- Endometritis after childbirth or abortion within past 3 months
- Current or recent (past 3 months) sexually transmitted infections including cervicitis
- Cervical or endometrial cancer
- Malignant gestational trophoblastic disease
- Unexplained vaginal bleeding
- Allergic reaction to any part of the copper IUD
- Less than 6 weeks postpartum
- Neurological or psychological conditions affecting pain sensation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Kasr Alainy medical school
Cairo, Egypt, 12111
Actively Recruiting
Research Team
A
Ahmed Maged
CONTACT
A
Ahmed chamel
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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