Trial · NCT07914296
Patient's Experience of Receiving Preoxygenation With the TTIM (Tube Tip in Mouth) Versus the Face Mask
NCT07914296, Not applicable, Not yet recruiting, Copenhagen University Hospital, Rigshospitalet
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. Patient's Experience of Receiving Preoxygenation With the TTIM (Tube Tip in Mouth) Versus the Face Mask. Trials, record NCT07914296. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07914296
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Patient's Experience of Receiving Preoxygenation With the TTIM (Tube Tip in Mouth) Versus the Face Mask
- NCT number
- NCT07914296
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 64 participants, estimated
- Lead sponsor
- Copenhagen University Hospital, Rigshospitalet
- Conditions
- Preoxygenation
- Interventions
- Preoxygenation by Breathing via the tip of a tube hold in the mouth (= Tube Tip In the Mouth (TTIM), Preoxygenation via Face mask
- First posted
- 2026-11-03
- Last updated
- 2026-11-03
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Comfort | From the start of the preoxygenation-procedure until the end of the preoxygenation-procedure | The participants reports on a 10-point scale from 1 = "Not uncomfortable at all" to 10 = Unbearable uncomfortable" |
| Secondary | Feeling of loss of control | From the start of the preoxygenation-procedure until the end of the preoxygenation-procedure | The participants reports on a 10-point scale from 1 = "No loss of control" to 10 = "Complete loss of control" |
| Secondary | Feeling of claustrophobia | From the start of the preoxygenation-procedure until the end of the preoxygenation-procedure | The participants reports on a 10-point scale from 1 = "no claustrophobia at all to 10 "Unbearable claustrophobia" |
| Secondary | End expiratory O2 obtained during the preoxygenation | From the start of the preoxygenation-procedure until the end of the preoxygenation-procedure | The End expiratory O2 obtained during the preoxygenation as measured via the anaesthesia machine |
| Secondary | Preference of technique | From the start of the preoxygenation-procedure until the end of the preoxygenation-procedure | The fraction of participants who prefer the TTIM (Tube Tip In Mouth) preoxygenation method over the face mask method |
| Secondary | Consider TTIM preferable for some patients | From the start of the preoxygenation-procedure until the end of the preoxygenation-procedure | The fraction of participants who considers that the TTIM techniques is preferable for some patients |
| Secondary | Considers that TTIM should be the default technique for preoxygenation | From the start of the preoxygenation-procedure until the end of the preoxygenation-procedure | The fraction of participants that considers that TTIM should be the default technique for preoxygenation (instead of face mask preoxygenation) |
| Secondary | Would consider implementing TTIM in own practice Yes/no | From the start of the preoxygenation-procedure until the end of the preoxygenation-procedure | The fraction of participants who would consider implementing TTIM in his own practice when giving preoxygenation to others in the future |
| Secondary | Number of encounters that the participating anaesthesiologist in his career has had patients who disliked the mask and would probably have preferred Tube tip in mouth (TTIM) as preoxygenation? | From the start of the preoxygenation-procedure until the end of the preoxygenation-procedure | Number of encounters that the participating anaesthesiologist in his career has had patients who disliked the mask and would probably have preferred Tube tip in mouth (TTIM) as preoxygenation? |
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/NCT07914296
GET https://conductscience.org/api/trials/v1/NCT07914296/registered