Effect of Cuminum Cyminum on the return of intestinal peristaltic movements after abdominal surgeries

Investigating the effect of Cuminum Cyminum on the return of intestinal peristaltic movements after abdominal surgeries in patients who hospitalized in the surgery ward of Ali Ibn Abi Taleb Hospital of Rafsanjan, 2021

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20150713023190N10

Enrollment

Registered

2021-10-24

Start date

2021-10-23

Completion date

Unknown

Last updated

2021-11-01

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

Conditions

Return of intestinal peristaltic movements. Absent bowel sounds

Interventions

Intervention 1: Intervention group: In this group, patients receive a 250 mg capsule of Cuminum Cyminum extract 4 hours after surgery and one hour after the first dose of this drug. Intervention 2: Co

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age between 18-60 years Candidate for abdominal surgery General anesthesia Inform consent for participate in the study

Exclusion criteria

Exclusion criteria: Use of Cuminum Cyminum permanently pregnancy and lactation Addiction Use of alcohol History of liver, kidney, heart and thyroid disorders Use of anticoagulant drugs Use of psychiatric drugs Gastric perforation

Design outcomes

Primary

Measure	Time frame
First gas passing. Timepoint: After the intervention. Method of measurement: Checklist (patient’ response will be recorded in the checklist).;First defecation. Timepoint: After the intervention. Method of measurement: Checklist.;Abdominal bloating. Timepoint: 2 hour after the intervention until 24 hours. Method of measurement: Checklist.;Abdominal pain. Timepoint: 2 hour after the intervention until 24 hours. Method of measurement: Checklist.;Nausea. Timepoint: 2 hour after the intervention until 24 hours. Method of measurement: Checklist.;Vomiting. Timepoint: 2 hour after the intervention until 24 hours. Method of measurement: Checklist.	—

Measure

Time frame

First gas passing. Timepoint: After the intervention. Method of measurement: Checklist (patient’ response will be recorded in the checklist).;First defecation. Timepoint: After the intervention. Method of measurement: Checklist.;Abdominal bloating. Timepoint: 2 hour after the intervention until 24 hours. Method of measurement: Checklist.;Abdominal pain. Timepoint: 2 hour after the intervention until 24 hours. Method of measurement: Checklist.;Nausea. Timepoint: 2 hour after the intervention until 24 hours. Method of measurement: Checklist.;Vomiting. Timepoint: 2 hour after the intervention until 24 hours. Method of measurement: Checklist.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmin Esmaeili Abdar

Rafsanjan University of Medical Sciences

amin31401@gmail.com+98 34 3425 5900

Outcome results

None listed

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