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NCT04596332
Central Venous Pressure Monitoring and Prognosis of High-risk Operating Patients
trial testing no intervention measures in Central Venous Pressure in 196 participants. Completed in 30 March 2020.
31 March 2018
Quick facts
| Lead sponsor | Fujian Provincial Hospital |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 196 |
| Start date | 1 February 2014 |
| Primary completion | 31 March 2018 |
| Estimated completion | 30 March 2020 |
Drugs / interventions tested
- no intervention measures
Conditions studied
- Central Venous Pressure — all drugs for Central Venous Pressure →
Sponsor
Fujian Provincial Hospital
Who can join
Adults 18 to 80, any sex, with Central Venous Pressure. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
While central venous pressure measurement is used to guide fluid management in high risk surgical patients during perioperative period, the relationship between the value of central venous pressure and organ dysfunction and prognosis of high-risk operating patients is unknow. In this study, we conducted a retrospective study of the relationship between the initial levels of CVP with organ dysfunction, the severity of illness, the length of ICU stay, and prognosis of critically ill patients.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Optimization of central venous pressure during the perioperative period is associated with improved prognosis of high-risk operation patients.
Wu J, Li J, Chen H, Shang X, et al · · 2023 · cited 3× · PMID 37188112 · DOI 10.1016/j.jointm.2022.06.003
Verify or expand the search:
- PubMed search for NCT04596332
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Central Venous Pressure
Currently open trials in the same condition.
- NCT06885073 — Non-invasive Central Venous Pressure Estimation in Pediatric Patients · NA · recruiting
- NCT06237751 — Preoperative Sildenafil Administration for Hepatectomy · NA · recruiting
Other Fujian Provincial Hospital trials
Trials by the same sponsor.
- NCT07471763 — Prospective Lifespan Cohort of Myocardial Infarction · not yet recruiting
- NCT07290764 — Survival Analysis of Surgical Resection Versus Observation in Patients With Initially uHCC Achieving CR After Systemic T · enrolling by invitation
- NCT07251114 — AI-assisted Endoscopic Ultrasound Grading of Early Esophageal Cancer Invasion Depth: A Multicenter, Prospective, Randomi · NA · recruiting
- NCT06564506 — Electroacupuncture for Preventing Postoperative Delirium in Older Adults Undergoing Total Knee Arthroplasty · NA · not yet recruiting
- NCT07380542 — Dynamic Magnesium Replacement Strategies and 28-Day Mortality in Non-Cardiac Critically Ill Patients With Hypomagnesemia · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04596332 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Fujian Provincial Hospital
- Last refreshed: 22 October 2020
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04596332.
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