Trials / Completed
CompletedNCT02769247
Efficacy of Intrauterine Lidocaine and Naproxen for Pain Control With Intrauterine Device Insertion
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 160 (actual)
- Sponsor
- Walter Reed National Military Medical Center · Federal
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
To compare the efficacy of intrauterine lidocaine and oral naproxen sodium on discomfort and pain of patients undergoing intrauterine device insertion.
Detailed description
This is a randomized, double-blind, placebo-controlled study with women that will be recruited from our outpatient obstetrics and gynecology clinic. Women desiring intrauterine device insertion will be invited to participate. The investigators plan to recruit women desiring intrauterine device insertion into one of four groups: A: placebo/normal saline infusion; B: placebo/lidocaine infusion; C: Saline infusion/ naproxen; D: lidocaine infusion/ naproxen.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Naproxen | Oral naproxen vs placebo |
| DRUG | Lidocaine | Intrauterine lidocaine vs normal saline |
| DRUG | placebo | either normal saline or empty oral capsule |
Timeline
- Start date
- 2014-06-01
- Primary completion
- 2016-12-01
- Completion
- 2016-12-01
- First posted
- 2016-05-11
- Last updated
- 2018-11-08
- Results posted
- 2018-11-08
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02769247. Inclusion in this directory is not an endorsement.