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Clinical Trial Summary

To investigate whether vaginal isonicotinic acid hydrazide (INH) administered before the levonorgestrel-releasing intrauterine system(IUs) insertion reduces failed insertions, insertion-related complications, and pain in Women With no Previous Vaginal Delivery.


Clinical Trial Description

Long-acting reversible contraception methods are highly effective methods for reduction of the unplanned pregnancy rate worldwide. The intrauterine device is a single procedure that provides reliable, effective and long term contraception for many women. However, the insertion procedure can be associated with a troublesome degree of pain that prevent some women from choosing its use. Different interventions have been described to decrease pain perception during intrauterine device insertion with no agreement on an effective one. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04500028
Study type Interventional
Source Aswan University Hospital
Contact
Status Completed
Phase Phase 4
Start date August 1, 2020
Completion date December 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
Completed NCT04499989 - Vaginal Isonicotinic Acid Hydrazide (INH) Administration Prior to T380A Intrauterine Device Insertion Phase 4
Completed NCT04505657 - Lidocaine Spray Plus Oral Celecoxib for Pain Control During Hysterosalpingography N/A
Not yet recruiting NCT04500002 - Isonicotinic Acid Hydrazide (INH) Pretreatment With Misoprostol Versus Misoprostol Alone in Missed Abortion 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