Trial · NCT01837498
Reversal of Neuromuscular Blockade in Thoracic Surgical Patients
NCT01837498, Completed, Endeavor Health
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Reversal of Neuromuscular Blockade in Thoracic Surgical Patients. Trials, record NCT01837498. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01837498
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Reversal of Neuromuscular Blockade in Thoracic Surgical Patients
- NCT number
- NCT01837498
- Status
- Completed
- Enrollment
- 200 participants, actual
- Lead sponsor
- Endeavor Health
- Conditions
- Residual Neuromuscular Blockade
- Interventions
- Neostigmine, Sugammadex
- First posted
- 2013-04-23
- Last updated
- 2020-02-13
Source ClinicalTrials.gov
Registered outcomes5
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Residual neuromuscular block (train-of-four ratio (TOF) < 0.9) | On admission to the postanesthesia care unit (PACU), up to 7 days | The incidence of residual neuromuscular block will be calculated on arrival to the PACU |
| Secondary | Time in operating room | participants will be followed for the duration of the operating room stay, an expected average of 2 hours, up to 7 days | |
| Secondary | Hypoxemic events | participants will be followed for the duration of the PACU stay, an expected average of 2 hours, up to 7 days | Blood oxygenation values will be measured using pulse oximetry from the time of PACU admission until discharge from the PACU |
| Secondary | Tests of muscle weakness | 15 and 30 minutes after admission to the PACU, up to 7 days | A standardized examination form will be used to determine the presence or absence of muscle weakness in a variety of muscle groups |
| Secondary | Length of stay in the PACU | participants will be followed for the duration of the PACU stay, an expected average of 2 hours, up to 7 days | The time required to meet discharge criteria and achieve actual discharge will be noted. |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 33323787 | DERIVED |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT01837498
GET https://conductscience.org/api/trials/v1/NCT01837498/registered