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NCT01690663 · ClinicalTrials.gov registry record · NA
Dose Response Study of Dexamethasone in Combination With Bupivacaine 0.25%
A NA study of Post-surgical Pain, sponsored by University of Pennsylvania.
- Completed
- Registry status
- NA
- Development phase
- 89
- Enrollment target
- 1
- Study location
NCT01690663 is a NA study of Post-surgical Pain that has completed, run by University of Pennsylvania. The registered enrollment target is 89 participants, below the 306-participant average among 4 other Post-surgical Pain trials with a reported enrollment target (71% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01690663, a NA study of Post-surgical Pain, has completed, sponsored by University of Pennsylvania.
- COMPLETED
- Registry status
- NA
- Development phase
- 89 participants
- Enrollment target
- 1
- Study location
Study Summary
When used in conjunction with a local anesthetic, dexamethasone may prolong both the sensory and motor effects of high supraclavicular brachial plexus nerve block (SBP) in arthroscopic shoulder surgery. This study seeks to determine if there is a relationship between the duration of sensory and motor blockade in supraclavicular brachial plexus nerve blocks (SBP) when combined with increasing doses of dexamethasone.
Conditions Studied
Interventions
- DRUG Dexamethasone
- DRUG normal saline
- DRUG Bupivacaine 0.25%
Study Locations (1)
Pennsylvania
- Penn Presbyterian Medical Center - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 89 participants |
| Start Date | 2012-09 |
| Est. Completion | 2015-02 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01690663
The ClinicalTrials.gov registry entry for NCT01690663 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 89 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 306-participant average among 4 other Post-surgical Pain trials with a reported enrollment target (71% lower). The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Post-surgical Pain appearing as the primary indexed condition, and to 3 interventions - of which Dexamethasone is the first listed.
NCT01690663 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT01690663 about?
NCT01690663 is a clinical study titled "Dose Response Study of Dexamethasone in Combination With Bupivacaine 0.25%". When used in conjunction with a local anesthetic, dexamethasone may prolong both the sensory and motor effects of high supraclavicular brachial plexus nerve block (SBP) in arthroscopic shoulder surgery. This study seeks to determine if there is a relationship between the duration of sensory and moto...
What is the current status of trial NCT01690663?
This trial is currently completed. It is a NA study. The enrollment target is 89 participants. The study started on 2012-09. Estimated completion is 2015-02.
What conditions does trial NCT01690663 study?
This clinical trial studies the following conditions: Post-surgical Pain.
What interventions are being tested in trial NCT01690663?
The interventions under investigation include: Dexamethasone (DRUG), normal saline (DRUG), Bupivacaine 0.25% (DRUG).
Who is sponsoring clinical trial NCT01690663?
This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01690663 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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