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NCT01881776 · ClinicalTrials.gov registry record · Early Phase 1
Continuous Interscalene Block Results in Superior Recovery Throughout the First Postoperative Week
A Early Phase 1 study of Postoperative Pain and Adverse Effects, sponsored by St. Luke's-Roosevelt Hospital Center.
- Completed
- Registry status
- Early Phase 1
- Development phase
- 71
- Enrollment target
- 1
- Study location
NCT01881776 is a Early Phase 1 study of Postoperative Pain and Adverse Effects that has completed, run by St. Luke's-Roosevelt Hospital Center. The registered enrollment target is 71 participants, below the 230-participant average among 63 other Postoperative Pain trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01881776, a Early Phase 1 study of Postoperative Pain and Adverse Effects, has completed, sponsored by St. Luke's-Roosevelt Hospital Center.
- COMPLETED
- Registry status
- Early Phase 1
- Development phase
- 71 participants
- Enrollment target
- 1
- Study location
Study Summary
The investigators undertook this prospective, randomized trial to compare the recovery profile throughout the first postoperative week in patients receiving continuous (CISB) interscalene brachial plexus block, single injection (SISB), or general anesthesia (GA) for arthroscopic rotator cuff repair surgery. Specifically, the effects of the three anesthetic techniques when used intraoperatively as a sole anesthesia modality were studied on postoperative pain, time-to-first pain, analgesic consumption, fast-tracked PACU bypass rate, length of PACU stay, time-to-discharge home, sleep duration, and related adverse effects. The investigators hypothesized that CISB results in a superior postoperative recovery profile as compared to SISB or GA alone.
Conditions Studied
Interventions
- PROCEDURE ISB
Study Locations (1)
New York
- St Luke's Roosevelt Hospital Center - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 71 participants |
| Start Date | 2011-08 |
| Est. Completion | 2012-06 |
| Phase | Early Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01881776
The ClinicalTrials.gov registry entry for NCT01881776 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 71 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 230-participant average among 63 other Postoperative Pain trials with a reported enrollment target (69% lower). The listed sponsor is St. Luke's-Roosevelt Hospital Center, which has 57 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Postoperative Pain appearing as the primary indexed condition, and to 1 intervention - of which ISB is the first listed.
NCT01881776 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT01881776 about?
NCT01881776 is a clinical study titled "Continuous Interscalene Block Results in Superior Recovery Throughout the First Postoperative Week". The investigators undertook this prospective, randomized trial to compare the recovery profile throughout the first postoperative week in patients receiving continuous (CISB) interscalene brachial plexus block, single injection (SISB), or general anesthesia (GA) for arthroscopic rotator cuff repair ...
What is the current status of trial NCT01881776?
This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 71 participants. The study started on 2011-08. Estimated completion is 2012-06.
What conditions does trial NCT01881776 study?
This clinical trial studies the following conditions: Postoperative Pain, Adverse Effects.
What interventions are being tested in trial NCT01881776?
The interventions under investigation include: ISB (PROCEDURE).
Who is sponsoring clinical trial NCT01881776?
This trial is sponsored by St. Luke's-Roosevelt Hospital Center, which has 57 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01881776 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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