Trial · NCT03854851
NALDEBAIN for Postoperative Pain Management in Take Down of Anastomosis
NCT03854851, Phase 4, Unknown, China Medical University Hospital
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. NALDEBAIN for Postoperative Pain Management in Take Down of Anastomosis. Trials, record NCT03854851. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03854851
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- NALDEBAIN for Postoperative Pain Management in Take Down of Anastomosis
- NCT number
- NCT03854851
- Status
- Unknown
- Phases
- Phase 4
- Enrollment
- 40 participants, estimated
- Lead sponsor
- China Medical University Hospital
- Conditions
- Postoperative Pain
- Interventions
- Naldebain, Morpine
- First posted
- 2019-02-26
- Last updated
- 2019-02-26
Source ClinicalTrials.gov
Registered outcomes10
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Supplemental analgesics | From Day 0 to Day 7 | The consumption of total amount (mg) of supplemental analgesics administered after surgery. |
| Secondary | Pain assessment: VAS | 2 hours after surgery | Using visual analog scale (VAS) with grades from 0 (no pain) to 10 (worst pain) |
| Secondary | Pain assessment: VAS | 6 hours after surgery | Using visual analog scale (VAS) with grades from 0 (no pain) to 10 (worst pain) |
| Secondary | Pain assessment: VAS | 24 hours after surgery | Using visual analog scale (VAS) with grades from 0 (no pain) to 10 (worst pain) |
| Secondary | Pain assessment: VAS | From Day 2 to Day 7 | Using visual analog scale (VAS) with grades from 0 (no pain) to 10 (worst pain), once daily |
| Secondary | Pain assessment: area under the curve of VAS | From post-OP to Day 7 | Pain assessment (time-specific pain intensity) calculated as the area under the curve of VAS pain intensity scores through 7 days after surgery |
| Secondary | Patient satisfaction: frequency of each option | Day 7 | Calculating the frequency of each option: highly satisfied, satisfied, uncertain, dissatisfied and very dissatisfied |
| Secondary | frequency of adverse event | From Day-1 to Day 7 | Recording the frequency of treatment-emergent adverse event (TEAE) |
| Other | Time of first farting | From post-OP to Day 7 | Observing when patients are able to pass gas after surgery |
| Other | Date of discharge | From post-OP to Day 7 | Observing when the condition of patients is good enough to discharge |
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/NCT03854851
GET https://conductscience.org/api/trials/v1/NCT03854851/registered