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Effect of meglumine versus placebo on improvement of symptoms of small bowel obstruction due to abdominal postoperative adhesions

Effect of meglumine versus placebo on improvement of symptoms of small bowel obstruction due to abdominal postoperative adhesions: a double blind randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201704259014N160
Enrollment
42
Registered
2017-05-02
Start date
2016-04-20
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

Bowel obstruction. Intestinal adhesions [bands] with obstruction

Interventions

Treatment - Drugs
Intervention 1: Intervention group: Nasogastric infusion of meglumine 500 ml for one hour. Intervention 2: Control group: Nasogastric infusion of dextrose water 500 ml for one hour.
Intervention group: Nasogastric infusion of meglumine 500 ml for one hour.
Control group: Nasogastric infusion of dextrose water 500 ml for one hour.

Sponsors

Vice-chancellor for Research and Technology, Hamadan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age of 18 to 65 years; small bowel obstruction due to abdominal postoperative adhesions. Exclusion criteria: Gastric cancer; colon obstruction; ileitis; indication of emergency surgery; peritonitis; inguinal hernia.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Assessing bowel obstruction. Timepoint: before intervention and 12, 24, and 48 hours after intervention. Method of measurement: through physical examination and taking history.;Assessing bowel obstruction. Timepoint: before intervention and 12, 24, and 48 hours after intervention. Method of measurement: through abdominal radiography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Parviz Majidi

Besat Hospital

harrisonpar@yahoo.com+98 81 3364 0030

Outcome results

None listed

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