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Clinical Trial Summary

To investigate whether vaginal isonicotinic acid hydrazide administered before intrauterine device (IUD) insertion reduces failed insertions, insertion-related complications and pain in in Women Delivered Only by Cesarean Delivery.


Clinical Trial Description

Women may experience pain and technical difficulties may be encountered when insertion of an intrauterine device is attempted through a narrow cervical canal. intrauterine device insertion- related complications and side effects are more common among women who had never delivered vaginally. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04499989
Study type Interventional
Source Aswan University Hospital
Contact
Status Completed
Phase Phase 4
Start date September 1, 2020
Completion date August 1, 2021

See also
  Status Clinical Trial Phase
Recruiting NCT04517890 - Transdermal Lidocaine Administration Prior to Insertion Levonorgestrel-releasing Intrauterine System N/A
Not yet recruiting NCT04505943 - Vaginal Misoprostol and Dinoprostone and Isonicotinic Acid Hydrazide Prior to Copper Intrauterine Device Insertion N/A
Not yet recruiting NCT04500002 - Isonicotinic Acid Hydrazide (INH) Pretreatment With Misoprostol Versus Misoprostol Alone in Missed Abortion N/A
Completed NCT04505657 - Lidocaine Spray Plus Oral Celecoxib for Pain Control During Hysterosalpingography N/A
Completed NCT04500015 - Vaginal Isonicotinic Acid Hydrazide Administration Prior to Intrauterine Device Insertion Phase 4
Not yet recruiting NCT04505917 - Vaginal Misoprostol and Dinoprostone Prior to Copper Intrauterine Device Insertion in Women N/A
Completed NCT04500028 - Vaginal Isonicotinic Acid Hydrazide Administration Prior to Insertion Levonorgestrel-releasing Intrauterine System Phase 4