the effect Probiotic in cutaneous complications of colostomy

The effect Probiotic in Local cutaneous complications In children with gastrointestinal ostoma

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

IRCT

Registry ID

IRCT20180306038983N1

Enrollment

Registered

2018-05-23

Start date

2016-04-12

Completion date

Unknown

Last updated

2018-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colostomy. Other Diseases Of Intestines

Interventions

Intervention 1: "Intervention group":After obtaining permission from the Ethics Committee of Mashhad University of Medical Sciences and receiving a written reference from the Mashhad Nursing and Midwi

Eligibility

Sex/Gender

All

Age

6 Months to 2 Years

Inclusion criteria

Inclusion criteria: pediatric with colostomy

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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.

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Secondary

Measure	Time frame
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.	—

Measure

Time frame

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.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahboobeh Ghasemirad

Mashhad University of Medical Sciences

Ghasemiradm931@mums.ac.ir+98 51 4466 8361

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026