Trial · NCT04161508
Enhanced Recovery After Surgery for Anterior Cervcial Spine Surgeries in Elderly Patients
NCT04161508, Not applicable, Unknown, Taipei Veterans General Hospital, Taiwan
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Enhanced Recovery After Surgery for Anterior Cervcial Spine Surgeries in Elderly Patients. Trials, record NCT04161508. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04161508
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Enhanced Recovery After Surgery for Anterior Cervcial Spine Surgeries in Elderly Patients
- NCT number
- NCT04161508
- Status
- Unknown
- Phases
- Not applicable
- Enrollment
- 100 participants, estimated
- Lead sponsor
- Taipei Veterans General Hospital, Taiwan
- Conditions
- Other Fusion of Spine, Cervical Region
- Interventions
- Sugammadex Injection, Neostigmine Injection
- First posted
- 2019-11-13
- Last updated
- 2019-11-13
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | mean time to 90% TOF ratio | up to postoperative 2 hour | time from injection of drug to train of four ratio to 90% |
| Primary | mean time to extubation | up to postoperative 3 day | time from injection of drug to tracheal extubation |
| Secondary | postoperative sorethroat | postoperative Day 1, 2,3,7,10,30 | verbal numerical rating scale (0\~10, 0 denotes no sorethroat; 10 denotes maximal sorethroat) |
| Secondary | postoperative dysphonia | postoperative Day 1, 2,3,7,10,30 | subjective assessment of voice change in horaseness, pitch, and loudness(0, 1, 2; 0 denotes none or no change; 1 denotes mild change; 2 denotes obvious change) |
| Secondary | postoperative dysphagia | postoperative Day 1, 2,3,7,10,30 | subjective assessment of dsyphagia by Bazaz classification (based on the easiness to swallow liquid or solid food, the severity is classified into none, mild, moderate and severe) |
| Other | postoperative muscle power | postoperative 2 hour, Day 1 | the grading of muscle power (MRC):0\~5, 0 denotes complete paralysis, 5 denote normal power |
| Other | time to left off bed | up to postoperative 14 day | time to patient can left off from bed |
| Other | time to remove foley catheter | up to postoperative 7 day | time to the foley catheter can be removed from patient |
| Other | complications | up to postoperative 14 day | any occurrence of global, respiratory and cardiovascular adverse events |
| Other | hospital day | up to postoperative 14 day | total day that patients are kept in the hospital |
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.
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 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/NCT04161508
GET https://conductscience.org/api/trials/v1/NCT04161508/registered