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The Effect of Mannitol on the Serum Potassium During Craniotomy

NCT03161977 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2017-07-31

No results posted yet for this study

Summary

This is an observational study designed to research the effect of mannitol on the concentration of intraoperative serum potassium in patients undergoing craniotomy, and to guide the safe use of mannitol during craniotomy.

Conditions

  • Mannitol Adverse Reaction
  • Hyperkalemia

Interventions

OTHER

Mannitol

Mannitol was intravenous infused within 15-20 mins when drilling skull

Sponsors & Collaborators

  • The Affiliated Hospital of Xuzhou Medical University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-01
Primary Completion
2017-06-01
Completion
2017-06-01

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03161977 on ClinicalTrials.gov