Trial · NCT00798018
Effect of Intra-cuff Lidocaine and Tetracaine on Tracheal Tube-induced Emergence Phenomena
NCT00798018, Not applicable, Completed, Sichuan University; results first posted 2009-12-18
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effect of Intra-cuff Lidocaine and Tetracaine on Tracheal Tube-induced Emergence Phenomena. Trials, record NCT00798018. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00798018
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effect of Intra-cuff Lidocaine and Tetracaine on Tracheal Tube-induced Emergence Phenomena
- NCT number
- NCT00798018
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 100 participants, actual
- Lead sponsor
- Sichuan University
- Conditions
- Pharyngitis
- Interventions
- 2% lidocaine, placebo, 1% tetracaine, N.S
- First posted
- 2008-11-25
- Last updated
- 2009-12-18
- Results first posted
- 2009-12-18
Source ClinicalTrials.gov
Registered outcomes1
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Visual Analogue Scale(0-100mm) by the Subject. | 6 hours, 12 hours, 24 hours, 48 hours after extubation | visual analogue scale (VAS) was used to evaluate the post-intubation sore throat. The VAS was a well-recongnized standard tool for rating of pain. The VAS measures exactly 100 mm. 0 means no pain and 100 means the worst pain that one can image. Patient marks a point on the line that matches the amount of pain he or she feels. |
Source ClinicalTrials.gov
Outcomes1
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Visual Analogue Scale(0-100mm) by the Subject. | 6 hours, 12 hours, 24 hours, 48 hours after extubation | mm | MEAN |
Source ClinicalTrials.gov
Results by group16
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Visual Analogue Scale(0-100mm) by the Subject. | Air Alone | 6h | 51 | Standard Deviation 37 | mm |
| Visual Analogue Scale(0-100mm) by the Subject. | Normal Saline | 6h | 40 | Standard Deviation 31 | mm |
| Visual Analogue Scale(0-100mm) by the Subject. | Lidocaine | 6h | 22 | Standard Deviation 17 | mm |
| Visual Analogue Scale(0-100mm) by the Subject. | Tetracaine | 6h | 9 | Standard Deviation 8 | mm |
| Visual Analogue Scale(0-100mm) by the Subject. | Air Alone | 12h | 50 | Standard Deviation 33 | mm |
| Visual Analogue Scale(0-100mm) by the Subject. | Normal Saline | 12h | 38 | Standard Deviation 19 | mm |
| Visual Analogue Scale(0-100mm) by the Subject. | Lidocaine | 12h | 25 | Standard Deviation 15 | mm |
| Visual Analogue Scale(0-100mm) by the Subject. | Tetracaine | 12h | 13 | Standard Deviation 7 | mm |
| Visual Analogue Scale(0-100mm) by the Subject. | Air Alone | 24h | 43 | Standard Deviation 39 | mm |
| Visual Analogue Scale(0-100mm) by the Subject. | Normal Saline | 24h | 41 | Standard Deviation 30 | mm |
1 to 10 of 16Source ClinicalTrials.gov
See all 16 results by groupParticipant flow12
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| Overall Study | STARTED | Air Alone | 25 | |
| Overall Study | STARTED | Normal Saline | 25 | |
| Overall Study | STARTED | Lidocaine | 25 | |
| Overall Study | STARTED | Tetracaine | 25 | |
| Overall Study | COMPLETED | Air Alone | 25 | |
| Overall Study | COMPLETED | Normal Saline | 25 | |
| Overall Study | COMPLETED | Lidocaine | 25 | |
| Overall Study | COMPLETED | Tetracaine | 25 | |
| Overall Study | NOT COMPLETED | Air Alone | 0 | |
| Overall Study | NOT COMPLETED | Normal Saline | 0 |
1 to 10 of 12Source ClinicalTrials.gov
See all 12 participant flowAdverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals12
The totals the trial posted for each group.
| Total | Group | Affected | At risk |
|---|---|---|---|
| Total, all-cause mortality | Air Alone | ||
| Total, all-cause mortality | Normal Saline | ||
| Total, all-cause mortality | Lidocaine | ||
| Total, all-cause mortality | Tetracaine | ||
| Total, other adverse events | Air Alone | 0 | 25 |
| Total, other adverse events | Normal Saline | 0 | 25 |
| Total, other adverse events | Lidocaine | 0 | 25 |
| Total, other adverse events | Tetracaine | 0 | 25 |
| Total, serious adverse events | Air Alone | 0 | 25 |
| Total, serious adverse events | Normal Saline | 0 | 25 |
1 to 10 of 12Source ClinicalTrials.gov
See all 12 adverse event totalsPapers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 14970135 | BACKGROUND |
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/NCT00798018
GET https://conductscience.org/api/trials/v1/NCT00798018/registered