Trial · NCT07891702
Effect of Transcutaneous Electrical Stimulation on Polysomnographic Parameters in Patients With Obstructive Sleep Apnea
NCT07891702, Not applicable, Recruiting, Mansoura University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effect of Transcutaneous Electrical Stimulation on Polysomnographic Parameters in Patients With Obstructive Sleep Apnea. Trials, record NCT07891702. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07891702
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effect of Transcutaneous Electrical Stimulation on Polysomnographic Parameters in Patients With Obstructive Sleep Apnea
- NCT number
- NCT07891702
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 50 participants, estimated
- Lead sponsor
- Mansoura University
- Conditions
- Obstructive Sleep Apnea
- Interventions
- Transcutaneous Electrical Stimulation
- First posted
- 2026-10-23
- Last updated
- 2026-10-23
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Change in Apnea-Hypopnea Index (AHI) | Baseline and within 1 week after baseline, during the second overnight polysomnography session with active electrical stimulation. | The change in the apnea-hypopnea index (AHI), defined as the number of apneas and hypopneas per hour of sleep, between baseline overnight polysomnography performed without electrical stimulation and the second overnight polysomnography performed during active transcutaneous electrical stimulation. AHI will be compared between the two sessions to evaluate the acute effect of electrical stimulation on OSA severity. |
| Secondary | Change in Oxygen Desaturation Index (ODI) | Baseline and within 1 week after baseline, during the second overnight polysomnography session. | The change in oxygen desaturation index (ODI), defined as the number of oxygen desaturation events per hour of sleep, between baseline polysomnography without electrical stimulation and polysomnography performed during active transcutaneous electrical stimulation. |
| Secondary | Change in Sleep Efficiency | Baseline and within 1 week after baseline, during the second overnight polysomnography session. | The change in sleep efficiency, calculated as total sleep time divided by total recording time in bed and expressed as a percentage, between baseline polysomnography and polysomnography performed during active transcutaneous electrical stimulation. |
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.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 21454399 | RESULT |
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/NCT07891702
GET https://conductscience.org/api/trials/v1/NCT07891702/registered