Trials / Completed
CompletedNCT03545893
Overnight Pain Treatment Investigating Opioids vs. Nonopioids
A Pilot Randomized Trial of Opioids Versus Nonopioids for Pain Control After Osmotic Dilator Placement for Abortion Care
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 70 (actual)
- Sponsor
- University of Pennsylvania · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare maximum pain scores between patients seeking induced abortion and requiring cervical preparation with osmotic dilators. Patients will be randomized to receive prescription for ibuprofen alone or to receive prescription for ibuprofen + oxycodone for overnight pain management after cervical preparation with osmotic dilators. Data collected in-person and through a text-messaging platform.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ibuprofen 600 mg | Ibuprofen 600mg prescription, to be taken 1 tablet as needed every 6 hours for pain. |
| DRUG | OxyCODONE 5 Mg Oral Tablet | Oxycodone 5mg Oral Tablet prescription, to be taken 1-2 tablets as needed every 6 hours for pain. |
Timeline
- Start date
- 2018-06-19
- Primary completion
- 2019-02-07
- Completion
- 2019-02-07
- First posted
- 2018-06-04
- Last updated
- 2020-03-25
- Results posted
- 2020-03-25
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03545893. Inclusion in this directory is not an endorsement.