Trial · NCT07904949
Registered outcomes11
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 11 of 11
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Quality of Recovery-15 (QoR-15) score | 24 hours after surgery | Validated 15-item patient-reported questionnaire assessing postoperative recovery quality. Total score ranges from 0-150; higher score indicates better postoperative recovery quality. |
| Secondary | Cumulative oral morphine equivalent (OME) consumption of rescue analgesics | 0 to 24 hours after surgery | Total cumulative rescue opioid analgesic consumption converted to oral morphine equivalent (OME) over the observation period. |
| Secondary | Time to first rescue analgesic requirement | Within 24 hours after surgery | Time interval from the end of surgery to the first administration of rescue analgesic medication for pain. |
| Secondary | Resting NRS pain score (0-10; higher=worse pain) | 0, 4, 8, 12, and 24 hours after surgery | Numeric Rating Scale (NRS) for pain; score range 0-10, 0 = no pain, 10 = worst imaginable pain; assessed at rest. |
| Secondary | Activity-evoked NRS pain score (passive knee flexion 45°) | 4, 8, 12, and 24 hours after surgery | Numeric Rating Scale (NRS) for pain (0-10; higher score = worse pain). Pain elicited by standardized passive knee flexion to 45 degrees. Not evaluable if regional block has not resolved. |
| Secondary | Maximal NRS pain score | 0 to 24 hours after surgery | The highest observed Numeric Rating Scale pain score within the observation window (resting pain). Score range 0-10; higher score represents worse pain. |
| Secondary | Time to first standardized out-of-bed mobilization | From the end of surgery until hospital discharge, approximately 1 day after surgery | Time interval from the end of surgery until completion of the first standardized out-of-bed mobilization (sitting, standing and walking ≥3 m under assistance). |
| Secondary | Post-operative night sleep quality score (0-10; higher=better sleep) | During the first night after surgery | Patient-reported sleep quality score, range 0-10; 0 = extremely poor sleep, 10 = excellent sleep. Assessed for the first night after surgery. |
| Secondary | Incidence of opioid-related adverse events (PONV, pruritus, urinary retention, over-sedation, respiratory depression) | 0 to 24 hours after surgery | Number / proportion of participants experiencing at least one opioid-related adverse event including postoperative nausea and vomiting (PONV), pruritus, urinary retention, over-sedation, respiratory depression. |
| Secondary | Incidence of intervention-related adverse events (ear pain, erythema, dizziness, palpitation) | During stimulation sessions and the first 24 hours after surgery | Number / proportion of participants experiencing adverse events related to taVNS intervention: ear pain, local skin erythema, dizziness, palpitation. |
| Secondary | Patient global satisfaction score (0-10; higher=higher satisfaction) | 24 hours after surgery | Patient-reported global satisfaction score, range 0-10; higher score indicates higher overall satisfaction with peri-operative care. |
Source ClinicalTrials.govtrials-2026-11-12-0.5.0
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 list from software.
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GET https://conductscience.org/api/trials/v1/NCT07904949/registered