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Clinical Trials/CTRI/2017/10/010089
CTRI/2017/10/010089
Completed
未知

Safety and efficacy of quick penetrating Heparin solution for prophylaxis against superficial venous cannula- A prospective, randomized, comparative clinical study.

PARUL INSTITUTE OF MEDICAL SCIENCE AND RESEARCH0 sites100 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: O- Medical and Surgical
Sponsor
PARUL INSTITUTE OF MEDICAL SCIENCE AND RESEARCH
Enrollment
100
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
September 15, 2018
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
PARUL INSTITUTE OF MEDICAL SCIENCE AND RESEARCH

Eligibility Criteria

Inclusion Criteria

  • Planned to undergo peripheral vein cannulation that has been planned to remain in situ for at least 48 hours of indoor period

Exclusion Criteria

  • 1\.Undergoing re\-cannulation due to phlebitis at earlier cannulation site 2\.Unconscious or comatose patients
  • 3\.History of hypersensitivity reaction to heparin or heparin induced thrombocytopenia
  • 4\. Signs of systemic infection, bacteremia
  • 5\. Planned administration of any of the following during study period:
  • 5\.1 Anti\-coagulants locally (in the cannula) or systemically.
  • 5\.2 NSAIDs locally over surrounding area
  • 6\. Participated in any clinical trial within last 30 days at the time of screening.
  • 7\. Any disorder or condition that in the opinion of investigator would prohibit study participation or affect study outcome.

Outcomes

Primary Outcomes

Not specified

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