Trials / Completed
CompletedNCT02943135
Lidocaine In-situ Gel Before Intrauterine Device Insertion
Effect of Self-administered Lidocaine In-situ Gel on Intrauterine Device Insertion Pain: A Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 120 (actual)
- Sponsor
- Assiut University · Academic / Other
- Sex
- Female
- Age
- 20 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
Intrauterine device can cause pain and discomfort in several ways: Use of the tenaculum to grasp the cervix and straighten the uterus for proper insertion; trans-cervical actions including measuring uterine depth, inserting the insertion tube, and removing the tube; and placement of the device in the uterus.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | lidocaine in-situ gel | lidocaine in-situ gel |
| DRUG | placebo in-situ gel | placebo in-situ gel |
Timeline
- Start date
- 2017-10-01
- Primary completion
- 2019-12-31
- Completion
- 2020-03-30
- First posted
- 2016-10-24
- Last updated
- 2020-05-20
Locations
2 sites across 1 country: Egypt
Source: ClinicalTrials.gov record NCT02943135. Inclusion in this directory is not an endorsement.