Trial · NCT06462313
Dobutamine for Management of Surgical Patients With Septic Shock
NCT06462313, Not applicable, Completed, First Affiliated Hospital of Zhejiang University
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Dobutamine for Management of Surgical Patients With Septic Shock. Trials, record NCT06462313. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06462313
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Dobutamine for Management of Surgical Patients With Septic Shock
- NCT number
- NCT06462313
- Status
- Completed
- Phases
- Not applicable
- Enrollment
- 584 participants, actual
- Lead sponsor
- First Affiliated Hospital of Zhejiang University
- Conditions
- Patients With Septic Shock, Surgical Patients, General Anesthesia
- Interventions
- Dobutamine, Norepinephrine
- First posted
- 2024-06-17
- Last updated
- 2025-12-04
Source ClinicalTrials.gov
Registered outcomes19
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Incidence of acute kidney injury after surgery | within 1 week after surgery | Incidence of acute kidney injury after surgery |
| Primary | Sequential Organ Failure Assessment (SOFA) score | Day 1 Day 3 and Day 7 in ICU after surgery | Sequential Organ Failure Assessment (SOFA) score, ranges from 0 to 24, with 24 being the worst |
| Primary | Mortality | in hospital and Day 28 and Day 90 after the surgery | Mortality |
| Secondary | Lactate level measurement | before surgery (0 hour), 1hour after begining of surgery and at the end of surgey | Lactate level measurement |
| Secondary | capillary filling time | before surgery (0 hour), 1hour after begining of surgery and at the end of surgey | capillary filling time |
| Secondary | Central venous oxygen saturation (ScvO2) | before surgery (0 hour), 1hour after begining of surgery and at the end of surgey | Central venous oxygen saturation (ScvO2) |
| Secondary | Urine volume | 1hour after begining of surgery and at the end of surgey | Urine volume |
| Secondary | Duration of norepinephrine intraoperatively | intraoperatively | Duration of norepinephrine intraoperatively |
| Secondary | Cumulative dose of norepinephrine intraoperatively | intraoperatively | Cumulative dose of norepinephrine intraoperatively |
| Secondary | Incidence of intraoperative arrythmia Incidence of intraoperative arrythmia | intraoperatively | Incidence of intraoperative arrythmia |
1 to 10 of 19Source ClinicalTrials.gov
See all 19 registered outcomesOutcomes0
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.
Papers11
The papers the trial lists on ClinicalTrials.gov.
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/NCT06462313
GET https://conductscience.org/api/trials/v1/NCT06462313/registered