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In the indwelling urinary catheterization (IUC), urinary leakage may develop around the catheter in the following days of catheterization. The volume and type of fluid used to inflate the catheter balloon has the potential to be a factor in the development of this problem.
In this study, the investigators aimed to investigate the effect of the type and amount of fluid used in inflating the silicone foley catheter balloon on the development of urinary leakage around the catheter. In addition to purpose, the following questions were answered to determine the optimal solution type and volume in inflating the balloon:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 10 ml sterile distilled water | Experimental | The indwelling urinary catheterization was inflated with 10 ml sterile distilled water (SDW) of the balloon. |
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| 15 ml sterile distilled water | Experimental | The indwelling urinary catheterization was inflated with 15 ml sterile distilled water (SDW) of the balloon. |
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| 10 ml 0.9% sodium chloride (NaCL) | Experimental | The indwelling urinary catheterization was inflated with 10 ml 0.9% sodium chloride (NaCL) of the balloon. |
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| 15 ml 0.9% sodium chloride (NaCL) | Experimental | The IUC was inflated with 15 ml 0.9% sodium chloride (NaCL) of the balloon. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| The use of different types and volumes of solutions to inflate the catheter balloon | Procedure | In catheterization procedure, catheter balloon was inflated according to the type and amount of fluid appropriate to the group to which the patient was assigned. |
| Measure | Description | Time Frame |
|---|---|---|
| Development of urine leakage around the catheter | Patients were followed up every 12 hours for the presence of urine leakage around the catheter. The presence of urine leakage was monitored by macroscopic examination, wetting of the diaper, and pH meter strip wrapped around the catheter. In addition, urine samples of the urine leakage were collected, and urine pH and leakage pH were compared. Participation of the patients in the study groups was continued until one or more of the following criteria met: Urinary leakage around the catheter, Termination of catheterization, Transferring the patient to another unit, Development of Exitus. | through study completion, about three years |
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Inclusion Criteria:
Exclusion Criteria:
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64 male and 64 female patients were included in the study.
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| Name | Affiliation | Role |
|---|---|---|
| Ayse AKBIYIK, PhD | İzmir Katip Çelebi University | Principal Investigator |
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