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UnknownNCT05707936

Normal Saline Versus Heparin Intermittent Flushing for the Prevention of Occlusion in Port-a-Cath

Normal Saline Versus Heparin Intermittent Flushing for the Prevention of Occlusion in Port-a-Cath: Randomized Controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
192 (estimated)
Sponsor
Chang Gung Memorial Hospital · Academic / Other
Sex
All
Age
20 Years
Healthy volunteers
Not accepted

Summary

Purpose: An evidence implementation of a randomized controlled trial for whether there is the difference in intermittent flushing 0.9% normal saline and heparin? Design: a single-blind randomized controlled trial Method: This study is based on the 5A (Ask, Acquire, Appraise, Apply, Audit) of evidence health care step, and design randomized controlled trial for evidence implementation. We will include inpatients over 20 years-old adults in New Taipei City TuCheng Hospital, Taiwan, who need administration medicine by port-a-catcher. The sample size is 192 according to G-power software. Random allocation software has using for block randomization, would assign to group A: flushing with 0.9% normal saline 10ml, group B: flushing with 0.9% normal saline 20ml, and group C: flushing with heparin 100 USP/ml. SPSS 20.0 software for statistical analysis, mean or standard deviation, one- way ANOVA would use.

Conditions

Interventions

TypeNameDescription
DRUGNormal Saline Flush 20 mlNormal Saline Flush 20 ml
DRUGNormal Saline Flush 10 mlNormal Saline Flush 10 ml
DRUGHeparin Flush (1000 USP, 10ml)Heparin Flush (1000 USP, 10ml)

Timeline

Start date
2023-02-01
Primary completion
2023-09-01
Completion
2023-12-31
First posted
2023-02-01
Last updated
2023-02-01

Source: ClinicalTrials.gov record NCT05707936. Inclusion in this directory is not an endorsement.