Trial · NCT06000137
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
1 to 12 of 12
Download this page as JSON| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | total | from the end of the surgery to 48 hours after surgery | no pain =0, mild pain =1-3, moderate pain =4-6, and severe pain =7-10 |
| Secondary | 24 hours amount of drug | From the time of use postoperative analgesic to the time of 24 hours after the surgery | the volume of postoperative analgesic in 24 hours after the surgery |
| Secondary | 48 hours pressing times of Patient-controlled Analgesia | From the time of use postoperative analgesic to the time of 48 hours after the surgery | the times of press analgesia pump in 24 hours after the surgery |
| Secondary | Visual Analogue Scale | at the time of 6 hours after the surgery | no pain =0, mild pain =1-3, moderate pain =4-6, and severe pain =7-10 |
| Secondary | Visual Analogue Scale | at the time of 12 hours after the surgery | no pain =0, mild pain =1-3, moderate pain =4-6, and severe pain =7-10 |
| Secondary | Visual Analogue Scale | at the time of 24 hours after the surgery | no pain =0, mild pain =1-3, moderate pain =4-6, and severe pain =7-10 |
| Secondary | Visual Analogue Scale | at the time of 48 hours after the surgery | no pain =0, mild pain =1-3, moderate pain =4-6, and severe pain =7-10 |
| Secondary | the incidence of nausea | from the time when patients use postoperative analgesic to the time when patients stop to use postoperative analgesic, assessed up to 48 hours | the incidence of nausea |
| Secondary | the incidence of vomiting | from the time when patients use postoperative analgesic to the time when patients stop to use postoperative analgesic, assessed up to 48 hours | the incidence of vomiting |
| Secondary | the incidence of dizziness | from the time when patients use postoperative analgesic to the time when patients stop to use postoperative analgesic, assessed up to 48 hours | the incidence of dizziness |
| Secondary | the incidence of urinary | from the time when patients use postoperative analgesic to the time when patients stop to use postoperative analgesic, assessed up to 48 hours | the incidence of urinary |
| Secondary | the incidence of respiratory depression | from the time when patients use postoperative analgesic to the time when patients stop to use postoperative analgesic, assessed up to 48 hours | the incidence of respiratory depression |
Source ClinicalTrials.govtrials-2026-11-12-0.4.0
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 list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT06000137/registered