IUD Insertion Complication Clinical Trial
Official title:
Postplacental LNG-IUD Ultrasound Use Study
This study will enroll women planning to have an intrauterine device (IUD) placed for contraception immediately following a vaginal delivery. Women will be randomized to have this procedure done with or without ultrasound guidance. We intend to determine if the routine use of ultrasound to confirm device position reduces the rates of IUD expulsion.
Participants will be screened and consented for participation in the study when they are admitted to Labor and Delivery for delivery and express desire for a post-placental LNG-IUD. If the patient consents for study participation and meets eligibility criteria above, she will be enrolled in the study after achieving vaginal delivery when she is randomized to either IUD insertion with ultrasound or without ultrasound use. See protocol for detailed description of IUD placement and ultrasound use. After placement of IUD with or without ultrasound guidance, patients will be scheduled for a routine postpartum follow-up visit 6-10 weeks after delivery. At the postpartum follow-up visit, providers will assess for IUD expulsion with usual clinical practice, including history, pelvic exam, and additional imaging if IUD strings are not visualized on exam. Several attempts to contact participants who do not attend their postpartum visits will be made to attempt to reschedule appointments and conduct a phone questionnaire assessing for IUD expulsion. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Not yet recruiting |
NCT03587077 -
Pain Relief During IUD Insertion in Women Delivered Only by Elective Cesarean Section
|
N/A | |
| Completed |
NCT04080336 -
Comparison of Vaginal Misoprostol and Dinoprostone Prior to Copper Intrauterine Device Insertion in Nulliparous Women
|
Phase 4 | |
| Not yet recruiting |
NCT02706509 -
Pain Management Associated With the Insertion of Jaydess® in Nulliparous Women
|
Phase 4 | |
| Recruiting |
NCT03828760 -
The Effectiveness of Music on Pain and Anxiety in IUD Insertion
|
N/A | |
| Withdrawn |
NCT01967017 -
Study of Local Anesthesia as a Method to Decrease IUD Insertion Related Pain
|
Phase 4 | |
| Completed |
NCT03111342 -
Intracervical Anesthesia and Pain Associated With Intrauterine Contraceptive Insertion
|
Phase 4 | |
| Completed |
NCT04963582 -
LI4 Acupuncture for Analgesia in Intrauterine Device Insertion
|
N/A | |
| Recruiting |
NCT02522130 -
Different Analgesics Prior to Intrauterine Device (IUD) Insertion: Is There Any Evidence?
|
N/A | |
| Completed |
NCT05594108 -
Ultrasound-guided IUD Insertion During Family Medicine Residency Training
|
N/A | |
| Recruiting |
NCT03939663 -
Role of Vaginal Misoprostol Prior to IUCD Insertion in Women Who Delivered Only by Elective Caesarean Section.
|
Phase 2 | |
| Recruiting |
NCT05875571 -
Intravenous Ketorolac Administration to Attenuate Post-procedural Pain Associated With Intrauterine Device Placement
|
Phase 4 | |
| Recruiting |
NCT05700812 -
IUD Placement Without Sounding
|
N/A | |
| Not yet recruiting |
NCT03362905 -
Lidocaine for Pain Control During Intrauterine Device Insertion
|
Phase 4 | |
| Recruiting |
NCT03724708 -
Comparing Expulsion Rates for Different Intrauterine Device Insertion Techniques
|
N/A | |
| Completed |
NCT02716636 -
Fast Versus Slow Tenaculum Placement
|
N/A |