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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: Completed Early Phase 1 study of Postoperative Pain and Adverse Effects, sponsored by St. Luke's-Roosevelt Hospital Center.
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 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
The effects of the three anesthetic techniques (continuous interscalene brachial plexus block (CISB), single interscalene brachial plexus block (SISB), or general anesthesia (GA)) when used intraoperatively as a sole anesthesia modality were studied on postoperative pain (highest NRS pain rating)
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 |
What the finished NCT01881776 record still lists
NCT01881776 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 71 participants, a relatively small participant target, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (69% lower).
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 a single indexed study location in 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.
Learn More About Clinical Trials
Similar trials for Postoperative Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT01881776's enrollment target sits among peer trials
71 85th of 120 higher than 36 of 120 other Postoperative Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Pain trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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