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NCT02860091 · ClinicalTrials.gov registry record
Blood Ropivacaine Concentrations Following Chest Wall Nerve Block Continuous Infusion
A clinical trial of Pain, Postoperative, sponsored by Boston Children's Hospital.
- Active
- Registry status
- 26
- Enrollment target
- 1
- Study location
NCT02860091 is a study of Pain, Postoperative that is active but no longer recruiting, run by Boston Children's Hospital. The registered enrollment target is 26 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (90% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02860091, a study of Pain, Postoperative, is active but no longer recruiting, sponsored by Boston Children's Hospital.
- ACTIVE NOT RECRUITING
- Registry status
- 26 participants
- Enrollment target
- 1
- Study location
Study Summary
The main objective of this proposed investigation is to evaluate blood ropivacaine concentrations in infants and toddlers following the initiation of, and over the course of, continuous paravertebral nerve blockade using ropivacaine infusion for postoperative pain control following esophageal atresia repair procedures that include posterior tracheopexy. Continuous unilateral chest wall nerve blockade (CUCWNB) using ropivacaine is the current standard of practice for this surgical population at the investigators' institution and, as such, this study does not aim to alter the current standard clinical care received by participants but rather evaluate the blood concentrations of ropivacaine as it is routinely used.
Conditions Studied
Interventions
- DRUG Ropivacaine infusion
Study Locations (1)
Massachusetts
- Boston Children"S Hospital - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 26 participants |
| Start Date | 2018-10-01 |
| Est. Completion | 2024-12 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02860091
The ClinicalTrials.gov registry entry for NCT02860091 describes a study currently listed as active not recruiting, categorized as an unspecified phase. The registered enrollment target is 26 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (90% lower). The listed sponsor is Boston Children's Hospital, which has 462 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Pain, Postoperative appearing as the primary indexed condition, and to 1 intervention - of which Ropivacaine infusion is the first listed.
NCT02860091 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT02860091 about?
NCT02860091 is a clinical study titled "Blood Ropivacaine Concentrations Following Chest Wall Nerve Block Continuous Infusion". The main objective of this proposed investigation is to evaluate blood ropivacaine concentrations in infants and toddlers following the initiation of, and over the course of, continuous paravertebral nerve blockade using ropivacaine infusion for postoperative pain control following esophageal atresi...
What is the current status of trial NCT02860091?
This trial is currently active not recruiting. The enrollment target is 26 participants. The study started on 2018-10-01. Estimated completion is 2024-12.
What conditions does trial NCT02860091 study?
This clinical trial studies the following conditions: Pain, Postoperative.
What interventions are being tested in trial NCT02860091?
The interventions under investigation include: Ropivacaine infusion (DRUG).
Who is sponsoring clinical trial NCT02860091?
This trial is sponsored by Boston Children's Hospital, which has 462 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02860091 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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