Trial · NCT07480785
TEAS Combined With Triple Antiemetic Drugs to Prevent PONV in High-Risk Patients
NCT07480785, Not applicable, Recruiting, Zhejiang University
3 sourcestrials-2026-11-12-0.4.0
Cite this record
ConductScience Library. TEAS Combined With Triple Antiemetic Drugs to Prevent PONV in High-Risk Patients. Trials, record NCT07480785. Release trials-2026-11-12-0.4.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07480785
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- TEAS Combined With Triple Antiemetic Drugs to Prevent PONV in High-Risk Patients
- NCT number
- NCT07480785
- Status
- Recruiting
- Phases
- Not applicable
- Enrollment
- 780 participants, estimated
- Lead sponsor
- Zhejiang University
- Conditions
- Uterine Fibroids (Leiomyoma), Ovarian Tumors, Gallstones
- Interventions
- transcutaneous electrical acupoint stimulation, Sham transcutaneous electrical acupoint stimulation, triple antiemetic drugs
- First posted
- 2026-03-18
- Last updated
- 2026-03-18
Source ClinicalTrials.gov
Registered outcomes4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Number of Participants Experiencing Nausea,Retching and Vomiting within 24 hours after operation. | 2 hours post-operation, 6 hours post-operation, 24 hours post-operation | The number of episodes of nausea, retching and vomiting within 24 hours after operation |
| Secondary | Number of Participants Experiencing Postoperative Nausea in 48 h Postoperatively | 2 hours post-operation, 6 hours post-operation, 24 hours post-operation, 48 hours post-operation | Nausea score: The severity of PON was measured using a visual analog scale (VAS), with 0 indicating no symptoms and 10 representing the most severe imaginable symptoms. |
| Secondary | Number of Participants Experiencing Postoperative Vomiting in 48 h Postoperatively | 2 hours post-operation, 6 hours post-operation, 24 hours post-operation, 48 hours post-operation | including retching and vomiting |
| Secondary | Need of Postoperative Metoclopramide | 2 hours post-operation, 6 hours post-operation, 24 hours post-operation, 48 hours post-operation | Need of Postoperative Metoclopramide |
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.
Source
- Release
- trials-2026-11-12-0.4.0
- Release manifest SHA-256
- 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4
- Registry capture
- 2026-11-12
- Results copy, AACT
- 2026-03-23
- NIH clinical studies file
- 2026-11-13
Source ClinicalTrials.gov
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNone 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/NCT07480785
GET https://conductscience.org/api/trials/v1/NCT07480785/registered