Clinical Trials Logo

Clinical Trial Summary

The purpose of this study is to observe the variation of Hemodynamics、lactic acid、base excess、peripheral vascular resistance and DO2 through FloTrac™/Vigileo™ system after rapid infusion mannitol in neurosurgery.The hemodynamic changes after mannitol infusion are shown in Figure 1. HR (Fig. 1A) and systolic BP (Figure 1B) significantly increased between 0 min and 10 min (P = 0.041) and between -10 min and 10 min (P = 0.073), respectively; these two variables decreased steadily and returned to the baseline. Diastolic BP (Fig. 1B) showed no significant change after mannitol infusion (P = 0.102). CVP (Fig. 1C) significantly increased between -20 min and 0 min (P < 0.001) and constantly decreased after 0 min, which remained below the baseline between 30 min and 60 min. CI (Fig. 1D) and SVI (Fig. 1E) showed a significant persistent increase between -20 min to 0 min (P < 0.001) and between -20 min and 10 min (P < 0.001), respectively. SVV exhibited a dipper-type change shown as a significant decrease between -20 min and 0 min and a significant increase between 0 min and 60 min (P < 0.001), which returned to the baseline after 20 min.


Clinical Trial Description

n/a


Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02237716
Study type Observational
Source First Affiliated Hospital, Sun Yat-Sen University
Contact
Status Active, not recruiting
Phase N/A
Start date June 2014
Completion date January 2015

See also
  Status Clinical Trial Phase
Not yet recruiting NCT02880566 - Efficacy of Scalp Block on Hemodynamic Stability and Opioid Consumption During Craniotomy N/A
Completed NCT05103735 - Propofol-remifentanyl Versus Dexmedetomidine in Awake Craniotomy: Impact on Electroclinical Seizure Activity
Completed NCT04285359 - Impact of Severe Intraoperative Hyperglycemia on Infection Rate After Elective Intracranial Interventions
Completed NCT03364283 - Sitting Versus Horizontal Position on Craniotomies
Completed NCT01502540 - Pain Prevalence After Major Craniotomy N/A
Recruiting NCT06157359 - Effect of SNB on the QoR in Patients Undergoing Supratentorial Tumor Resection N/A
Recruiting NCT01474304 - Intravenous Acetaminophen for Craniotomy Patients Phase 2
Completed NCT01617837 - The Efficacy of P6 Acupressure in Reducing Postoperative Nausea and Vomiting in Patients Undergoing Craniotomy Phase 2/Phase 3
Recruiting NCT04229966 - Prospective, Observational Real-world Treatments of AEDH in Large-scale Surgical Cases
Completed NCT01987648 - eCRANIO Trial Study on Elective CRAniotomies: Postoperative Neurointensive Care, Imaging and Outcome
Recruiting NCT05962684 - A Greek-designed ERAS Protocol in Elective Craniotomy
Recruiting NCT04261673 - Prospective Randomized Evaluation of Decompressive Ipsilateral Craniectomy for Traumatic Acute Epidural Hematoma N/A
Completed NCT05940935 - The Relationship of Developing Metabolic Acidosis With Antiepleptic Drugs in Craniotomy Operations
Completed NCT03033706 - Intraoperative Goal Directed Fluid Management in Supratentorial Brain Tumor Craniotomy N/A
Completed NCT00658242 - Craniofacial Surgery Perioperative Registry N/A
Completed NCT04859907 - Bone Flap Fixation Systems For Craniotomy Procedures N/A
Recruiting NCT01966939 - Influences of Types of Skull Surgery on Temporomandibular Joint Performance N/A
Completed NCT01606969 - Comparison of Epinephrine-lidocaine Solution and Dexmedetomidine -Lidocaine Solution N/A
Completed NCT00590499 - Agitation in Post Operative Neurosurgical Patients N/A
Withdrawn NCT01282645 - Case Series to Evaluate Patient Specific Implants (PSI) in Polyether Ether Ketone (PEEK) Performance After 2 Years N/A