Contraception
Conditions
Brief summary
Different studies have been made in an attempt to reduce the pain and the duration of the process of outpatient insertion of the intrauterine device. in this trial, the investigators aim to insert the IUD under ultrasonographic guidance, which can help to reduce the pain, decrease the process of insertion, in addition, it reduces the incidence of malposition of IUD as well as the risk of complications.
Interventions
Sponsors
Woman's Health University Hospital, Egypt
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
20 Years to 45 Years
Healthy volunteers
Yes
Inclusion criteria
* Females desiring contraception with the use of IUD
Exclusion criteria
* Are pregnant or think they may be pregnant * Septic pregnancy or abortion * Have unexplained abnormal vaginal bleeding * Have untreated cervical cancer * Have malignant gestational trophoblastic disease * Have uterine cancer * Have uterine abnormalities * Have or may have had a pelvic infection within the past three months * Have or may have any sexually transmitted disease * Have pelvic tuberculosis * Are postpartum between 48 hours and 4 weeks * Have benign gestational trophoblastic disease * Have ovarian cancer * Have AIDS (unless clinically well on anti-retroviral therapy)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Assessment of degree of pain during IUD insertion | 6 months | Pain will be assessed by the use of visual analog scale, Pain rating scale |
Countries
Egypt
Outcome results
None listed