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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02214316
Other study ID # 201408006
Secondary ID
Status Terminated
Phase Phase 1/Phase 2
First received August 7, 2014
Last updated April 27, 2016
Start date October 2015

Study information

Verified date April 2016
Source Washington University School of Medicine
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Children with concussion may improve with intravenous fluids.


Recruitment information / eligibility

Status Terminated
Enrollment 2
Est. completion date
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 6 Years to 18 Years
Eligibility Inclusion Criteria:

- History of acute concussion

Exclusion Criteria:

- Other significant medical illness

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Hypertonic Saline


Locations

Country Name City State
United States Washington University School of Medicine St. Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postconcussive symptoms 3 months No