Investigating the effect of lactulose on improving ileus after abdominal surgeries

Investigating the effect of lactulose on improving ileus after abdominal surgeries; Clinical trial study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20241106063626N1

Enrollment

Registered

2024-12-02

Start date

2024-07-10

Completion date

Unknown

Last updated

2025-01-08

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

Conditions

Postoperative Ileus.

Interventions

Intervention 1: Intervention group: 30 patients scheduled for abdominal surgery will be evaluated after obtaining informed consent and receiving the relevant ethical codes from the ethics committee. A

Eligibility

Sex/Gender

All

Age

18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients undergoing abdominal surgery with midline incision Patients aged between 18-65

Exclusion criteria

Exclusion criteria: Critically ill patients with neuromuscular problems who are unable to move Patients who are not conscious and do not communicate or have mental retardation Lack of consent for intervention Pregnant patients

Design outcomes

Primary

Measure	Time frame
Gas passage. Timepoint: At intervals of 12 , 24 , and 36 hours. Method of measurement: Checklist.;Defication. Timepoint: At intervals of 12 , 24 , and 36 hours. Method of measurement: Checklist.;Return of bowel movements and auscultation of bowel sounds. Timepoint: At intervals of 12 , 24 , and 36 hours. Method of measurement: Checklist.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirhossein Jamali

Mazandaran University of Medical Sciences

a.jamali@mazums.ac.ir+98 11 3354 3246

Outcome results

None listed

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