Trial · NCT01941628
Comparison of Surgical Conditions in Cesarean Section Under General Anesthesia With Deep Neuromuscular Blockade Versus Succinylcholine
NCT01941628, Phase 4, Completed, Charles University, Czech Republic; results first posted 2019-02-11
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Comparison of Surgical Conditions in Cesarean Section Under General Anesthesia With Deep Neuromuscular Blockade Versus Succinylcholine. Trials, record NCT01941628. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01941628
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Comparison of Surgical Conditions in Cesarean Section Under General Anesthesia With Deep Neuromuscular Blockade Versus Succinylcholine
- NCT number
- NCT01941628
- Status
- Completed
- Phases
- Phase 4
- Enrollment
- 91 participants, actual
- Lead sponsor
- Charles University, Czech Republic
- Conditions
- Cesarean Section
- Interventions
- Rocuronium, Succinylcholine
- First posted
- 2013-09-13
- Last updated
- 2019-02-11
- Other registries' IDs
- eudract:2013-003077-97
- Results first posted
- 2019-02-11
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Induction to Delivery Interval | 24 hrs | Induction to delivery interval will be used as primary keypoint for surgical conditions comparison. |
| Primary | Number of Participants With Newborn in Need of Respiratory Support | 24 hours | The number of participants with a newborn in need of respiratory support will be the primary safety measure in comparison of the influence of different neuromuscular blockade levels on newborn adaptation. |
| Secondary | Peroperative and Postoperative Surgical Complication | 5 days | A total number of surgical complications evaluated at day 5 after Caesarean delivery. |
Source ClinicalTrials.gov
Outcomes3
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Induction to Delivery Interval | 24 hrs | seconds | MEAN | |
| PRIMARY | Number of Participants With Newborn in Need of Respiratory Support | 24 hours | The number of participants with a newborn in need of respiratory support | participants | NUMBER |
| SECONDARY | Peroperative and Postoperative Surgical Complication | 5 days | participants | NUMBER |
Source ClinicalTrials.gov
Results by group6
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Induction to Delivery Interval | Rocuronium | 268 | Standard Deviation 73 | seconds | |
| Induction to Delivery Interval | Succinylcholine | 276 | Standard Deviation 63 | seconds | |
| Number of Participants With Newborn in Need of Respiratory Support | Rocuronium | 0 | participants | ||
| Number of Participants With Newborn in Need of Respiratory Support | Succinylcholine | 0 | participants | ||
| Peroperative and Postoperative Surgical Complication | Rocuronium | 0 | participants | ||
| Peroperative and Postoperative Surgical Complication | Succinylcholine | 0 | participants |
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 | Rocuronium | 46 | |
| Overall Study | STARTED | Succinylcholine | 45 | |
| Overall Study | COMPLETED | Rocuronium | 45 | |
| Overall Study | COMPLETED | Succinylcholine | 45 | |
| Overall Study | NOT COMPLETED | Rocuronium | 1 | |
| Overall Study | NOT COMPLETED | Succinylcholine | 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 | Rocuronium | 0 | 45 |
| Total, all-cause mortality | Succinylcholine | 0 | 45 |
| Total, other adverse events | Rocuronium | 0 | 45 |
| Total, other adverse events | Succinylcholine | 0 | 45 |
| Total, serious adverse events | Rocuronium | 0 | 45 |
| Total, serious adverse events | Succinylcholine | 0 | 45 |
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 comparisons4
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|---|
| Rocuronium vs Succinylcholine: Peroperative and Postoperative Surgical Complication | Trial comparisons |
| Rocuronium vs Succinylcholine: Number of Participants With Newborn in Need of Respiratory Support | Trial comparisons |
| Rocuronium vs Succinylcholine: deaths from any cause | Trial comparisons |
| Rocuronium vs Succinylcholine: 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/NCT01941628
GET https://conductscience.org/api/trials/v1/NCT01941628/registered