Trial · NCT02635542
Effect of Neuromuscular Blockade on Pulmonary Complications in Elective Cardiac Surgery
NCT02635542, Phase 4, Completed, University of Chicago; results first posted 2018-07-17
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effect of Neuromuscular Blockade on Pulmonary Complications in Elective Cardiac Surgery. Trials, record NCT02635542. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02635542
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effect of Neuromuscular Blockade on Pulmonary Complications in Elective Cardiac Surgery
- NCT number
- NCT02635542
- Status
- Completed
- Phases
- Phase 4
- Enrollment
- 100 participants, actual
- Lead sponsor
- University of Chicago
- Conditions
- Neuromuscular Blockade, Postoperative Complications
- Interventions
- Succinylcholine, Cisatracurium
- First posted
- 2015-12-21
- Last updated
- 2018-07-17
- Results first posted
- 2018-07-17
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of Participants With Postoperative Pulmonary Complications | 72 hours following surgical procedure | Having at least one of the following complications, determined according to pre-specified criteria: extubation delayed \>24hrs, reintubation, mechanical respiratory support, pneumonia, aspiration, ARDS (Acute Respiratory Distress Syndrome), or mortality from respiratory arrest. |
| Secondary | Surgical Conditions | During general anesthesia | Assessed by surgeon questionnaire designed for study to determine any negative effects impeding the progress of surgery or safety, on scale of 1=poor to 5=excellent |
Source ClinicalTrials.gov
Outcomes2
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Number of Participants With Postoperative Pulmonary Complications | 72 hours following surgical procedure | Participants | COUNT_OF_PARTICIPANTS | |
| SECONDARY | Surgical Conditions | During general anesthesia | 2 participants in the CIS group and 4 participants in the SUX group had missing data for this outcome. | units on a scale | MEAN |
Source ClinicalTrials.gov
Results by group4
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Number of Participants With Postoperative Pulmonary Complications | Group CIS | 8 | Participants | ||
| Number of Participants With Postoperative Pulmonary Complications | Group SUX | 8 | Participants | ||
| Surgical Conditions | Group CIS | 4.96 | Standard Deviation 0.20 | units on a scale | |
| Surgical Conditions | Group SUX | 4.65 | Standard Deviation 0.85 | units on a scale |
Source ClinicalTrials.gov
Participant flow6
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Group CIS | 50 | |
| Overall Study | STARTED | Group SUX | 50 | |
| Overall Study | COMPLETED | Group CIS | 50 | |
| Overall Study | COMPLETED | Group SUX | 50 | |
| Overall Study | NOT COMPLETED | Group CIS | 0 | |
| Overall Study | NOT COMPLETED | Group SUX | 0 |
Source ClinicalTrials.gov
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 totals6
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Group CIS | 0 | 50 |
| Total, all-cause mortality | Group SUX | 0 | 50 |
| Total, other adverse events | Group CIS | 0 | 50 |
| Total, other adverse events | Group SUX | 0 | 50 |
| Total, serious adverse events | Group CIS | 0 | 50 |
| Total, serious adverse events | Group SUX | 0 | 50 |
Source ClinicalTrials.gov
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
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 comparisons3
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Group CIS vs Group SUX: Number of Participants With Postoperative Pulmonary Complications | Trial comparisons |
| Group CIS vs Group SUX: deaths from any cause | Trial comparisons |
| Group CIS vs Group SUX: serious adverse events | Trial comparisons |
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/NCT02635542
GET https://conductscience.org/api/trials/v1/NCT02635542/registered