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NCT06948409 · ClinicalTrials.gov registry record
NMBA Reversal and Postoperative Urinary Retention
A clinical trial of Neuromuscular Blockade and Urinary Retention Postoperative, sponsored by Beth Israel Deaconess Medical Center.
- Active
- Registry status
- 70,000
- Enrollment target
- 1
- Study location
NCT06948409: Active study of Neuromuscular Blockade and Urinary Retention Postoperative, sponsored by Beth Israel Deaconess Medical Center.
NCT06948409 is a study of Neuromuscular Blockade and Urinary Retention Postoperative that is active but no longer recruiting, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 70,000 participants, above the 174-participant average among 6 other Neuromuscular Blockade trials with a reported enrollment target (40130% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06948409, a study of Neuromuscular Blockade and Urinary Retention Postoperative, is active but no longer recruiting, sponsored by Beth Israel Deaconess Medical Center.
- ACTIVE NOT RECRUITING
- Registry status
- 70,000 participants
- Enrollment target
- 1
- Study location
Study Summary
In this single-center retrospective cohort study of adult patients who underwent surgery under general anesthesia at Beth Israel Deaconess Medical Center between September 2016 and January 2024, the association between the choice of neuromuscular blocking agent (NMBA) reversal strategy, comparing sugammadex with neostigmine (combined with a muscarinic antagonist), and postoperative urinary retention (POUR) will be evaluated. In secondary analyses, the effects of NMBA reversal strategy and POUR on costs of care and unplanned hospital visits will be analyzed.
Primary Outcome
The primary outcome, post-anesthesia care unit (PACU) discharge delay due to postoperative urinary (POUR), will be defined as a documented delay in PACU discharge due to the inability to void. The PACU nurses or physicians responsible for immediate postoperative care routinely document these delays. Documentation about delays is required before a patient is discharged from the PACU. Within the individual categories "renal", "urinary", and "other", the investigators will search through all free t
Conditions Studied
Interventions
- DRUG Choice of reversal agent (sugammadex or neostigmine [with muscaranic antagonist])
Study Locations (1)
Massachusetts
- Beth Israel Deaconess Medical Center - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 70,000 participants |
| Start Date | 2025-06-08 |
| Est. Completion | 2026-06-01 |
What the registry record for NCT06948409 still lists
NCT06948409 is an observational study that tracks outcomes without assigning an intervention. Its 70,000 participants enrollment target places it among the larger protocols in the corpus, above the 174-participant average among 6 other Neuromuscular Blockade trials with a reported enrollment target (40130% higher).
The record links to 10 conditions, with Neuromuscular Blockade appearing as the primary indexed condition, and to 1 intervention - of which Choice of reversal agent (sugammadex or neostigmine [with muscaranic antagonist]) is the first listed.
NCT06948409 reports a single indexed study location in Massachusetts.
Frequently Asked Questions
What is clinical trial NCT06948409 about?
NCT06948409 is a clinical study titled "NMBA Reversal and Postoperative Urinary Retention". In this single-center retrospective cohort study of adult patients who underwent surgery under general anesthesia at Beth Israel Deaconess Medical Center between September 2016 and January 2024, the association between the choice of neuromuscular blocking agent (NMBA) reversal strategy, comparing su...
What is the current status of trial NCT06948409?
This trial is currently active not recruiting. The enrollment target is 70,000 participants. The study started on 2025-06-08. Estimated completion is 2026-06-01.
What conditions does trial NCT06948409 study?
This clinical trial studies the following conditions: Neuromuscular Blockade, Urinary Retention Postoperative, Sugammadex, Neuromuscular Blocking Agents, Urinary Retention After Procedure.
What interventions are being tested in trial NCT06948409?
The interventions under investigation include: Choice of reversal agent (sugammadex or neostigmine [with muscaranic antagonist]) (DRUG).
Who is sponsoring clinical trial NCT06948409?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06948409 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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