Trials / Terminated
TerminatedNCT02962427
Treatment of Post-dural Puncture Headache in Postpartum Patients: Sphenopalatine Ganglion Block to Epidural Blood Patch.
Treatment of Post-dural Puncture Headache in Postpartum Parturients: Comparing Sphenopalatine Ganglion Block to Epidural Blood Patch.
- Status
- Terminated
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 4 (actual)
- Sponsor
- University of Colorado, Denver · Academic / Other
- Sex
- Female
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this research study is to compare the effectiveness of a sphenopalatine ganglion block to an epidural blood patch for post-dural puncture headache relief in randomized postpartum parturients over a 48 hour period.
Detailed description
The purpose of this research study is to compare the effectiveness of a sphenopalatine ganglion block to an epidural blood patch for post-dural puncture headache relief in randomized postpartum parturients over a 48 hour period. A known dural puncture is defined as free flow of cerebral spinal fluid (CSF) during neuraxial placement. An unknown dural puncture is defined as neuraxial placement where free flow of CSF is not appreciated, however the patient is diagnosed with a post-dural puncture headache as defined by the International Classification of Headache Disorders.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Sphenopalatine ganglion Block | |
| PROCEDURE | Epidural blood patch |
Timeline
- Start date
- 2016-11-01
- Primary completion
- 2018-12-01
- Completion
- 2018-12-01
- First posted
- 2016-11-11
- Last updated
- 2020-01-23
- Results posted
- 2020-01-23
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02962427. Inclusion in this directory is not an endorsement.