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The effect of coffee consumption on improving bowel function after abdominal hysterectomy compared to routine nutritional regime

The effect of coffee consumption on improving bowel function after abdominal hysterectomy compared to routine nutritional regime

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200116046153N1
Enrollment
40
Registered
2020-04-04
Start date
2020-09-22
Completion date
Unknown
Last updated
2020-04-21

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

Conditions

Ileus after abdominal hysterectomy.

Interventions

Intervention 1: Intervention group: In the intervention group, in the morning after surgery, in addition to routine measures, 100 ml coffee drink (5 g) of Nestle branded coffee is consumed by the pati

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Patients undergoing abdominal hysterectomy due to benign disease The duration of surgery is less than 2 and a half hours

Exclusion criteria

Exclusion criteria: Allergies or allergies to caffeine compounds Inflammatory bowel disease Liver dysfunction Heart arrhythmia Chronic constipation History of bowel surgery Abdominal radiotherapy or intraperitoneal chemotherapy history Patient transfer to ICU after abdominal hysterectomy Need to insert NGT during web immediately after hysterectomy Hypertension

Design outcomes

Primary

MeasureTime frame
The time of the patient's first gas discharge. Timepoint: Every 8 hours after intervention. Method of measurement: The patient is instructed to announce the time of first gas excretion.;Time to first bowel movements. Timepoint: Every 8 hours after intervention. Method of measurement: Control of the timing of the first intestinal movements by the researcher by checking the timing of the onset of intestinal sounds.;Time to first defication. Timepoint: Every 8 hours after intervention. Method of measurement: The patient is instructed to announce the time of first defication.;Time to solid diet tolerance. Timepoint: Every 8 hours after intervention. Method of measurement: Controlling patient solid diet tolerance time by a researcher.;Length of stay in hospital. Timepoint: daily after intervention. Method of measurement: Controlling the number of days a patient is hospitalized by the researcher.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactzahra behnam rassouli

Mashhad University of Medical Sciences

zbehnam71@gmail.com+98 51 3605 0557

Outcome results

None listed

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