the effect Probiotic in cutaneous complications of colostomy

Phase 4

• Conditions: Colostomy.; Other Diseases Of Intestines; K55-K64

• Registration Number: IRCT20180306038983N1
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 18 June 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

pediatric with colostomy

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Checker tool score the skin around the colostomy. Timepoint: . Before the intervention, the fourth day of intervention, after the end of the care period and one week after the probiotic has stopped, the Ostomy Skin Tool will be checked. Method of measurement: a tool for checking skin around colostomy(SST).;Stool acidity. Timepoint: Before the intervention, the fourth day of intervention, after the end of the care period and one week after the interruption of the probiotic, a fecal analysis test will be performed. Method of measurement: Stool analysis test.

Secondary Outcome Measures

Name	Time	Method
Skin color around colostomy. Timepoint: Before the intervention, the fourth day of intervention, after the completion of the care period and one week after the interruption of the probiotic. Method of measurement: See researcher.;Stool color. Timepoint: Before the intervention, the fourth day of intervention, after the completion of the care period and one week after the interruption of the probiotic. Method of measurement: See researcher.;Consistency of stool. Timepoint: Before the intervention, the fourth day of intervention, after the completion of the care period and one week after the interruption of the probiotic. Method of measurement: See researcher.