Trial · NCT07891299
VR During Chest Tube Removal After CABG
NCT07891299, Not applicable, Completed, Maltepe University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. VR During Chest Tube Removal After CABG. Trials, record NCT07891299. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07891299
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- VR During Chest Tube Removal After CABG
- NCT number
- NCT07891299
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 82 participants, actual
- Lead sponsor
- Maltepe University
- Conditions
- Coronary Artery Bypass Graft Surgery(CABG), Postoperative Pain Management
- Interventions
- VR Shinecon G04EA Virtual Reality Headset
- First posted
- 2026-10-23
- Last updated
- 2026-10-26
Source ClinicalTrials.gov
Registered outcomes2
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Pain Intensity (VAS) | Immediately before and immediately after chest tube removal | Pain intensity is assessed using the Visual Analog Scale (VAS), with scores ranging from 0 to 10. A score of 0 indicates no pain, while a score of 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity. |
| Secondary | Anksiyete - State-Trait Anxiety Inventory (STAI-State) | Before chest tube removal (baseline) and immediately after completion of chest tube removal (post-intervention). | Anxiety is assessed using the State Anxiety Inventory (STAI-State). Total scores range from 20 to 80, with higher scores indicating greater levels of state anxiety. |
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/NCT07891299
GET https://conductscience.org/api/trials/v1/NCT07891299/registered