Appendicostomy colonic irrigation by pump

Evaluation the effect of pump to reduce the time required for the appandicostomy colonic irrigation in patients with fecal incontinence compared to the traditional method.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2013020810519N2

Enrollment

Registered

2013-03-09

Start date

2013-02-18

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Fecal incontinence. Faecal incontinence

Interventions

Intervention 1: Patients were divided into 2 groups. In the first group, each patient is asked to perform traditional colon irrigation. In this method, 1 liter fluid infused trans appendicostomy by gr

Lifestyle

Patients were divided into 2 groups. In the first group, each patient is asked to perform traditional colon irrigation. In this method, 1 liter fluid infused trans appendicostomy by gravity into the c

Patients were divided into 2 groups. In the second group, each patient is asked to perform colon irrigation by pump. In This method, 1 liter water infused into the colon by pump. Patients after each c

Eligibility

Sex/Gender

All

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patient consent to inclusion. there is appendicostomy or any type of ostomy for colon irrigation(cecostomy, neoappendicostomy). at least 2 months using appendicostomy colon irrigation. no case of known case of psychological disease. Exclusion criteria: Patient dissatisfaction to entering or Continue participation in the study. Complications during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Colon irrigation time. Timepoint: Exactly after intervention. Method of measurement: minute.;Volume of infusion for colon irrigation. Timepoint: Exactly after intervention. Method of measurement: ml.;CCF-FI score. Timepoint: one week after intervention. Method of measurement: according to CCF-FIS guideline.	—

Secondary

Measure	Time frame
Duration of excretion after the injected fluid. Timepoint: exactly after intervention. Method of measurement: minute.;Abdominal pain. Timepoint: during fluid injection(intervention). Method of measurement: positive-negative.;Nausea. Timepoint: during intervention. Method of measurement: positive-nagative.;Fluid infusion time. Timepoint: exactly after intervention. Method of measurement: minute.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyed Hamzeh Mousavi

Tehran University of Medical Sciences

shm135978@yahoo.com+98 21 6435 2215

Outcome results

None listed

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