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Comparison early oral feeding with delayed oral feeding in elective GI surgery

Comparison the outcomes of early oral feeding with delayed oral feeding in patients undergoing elective GI surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190529043758N1
Enrollment
200
Registered
2019-07-28
Start date
2017-08-23
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Condition 1: Jejunojejunostomy. Condition 2: Loop gastrojejunostomy + Braun jejunojejunostomy. Condition 3: Ileoileostomy. Condition 4: Total colectomy. Condition 5: choldoduodenostomy. Condition 6: Jejunoileal anastomosis.

Interventions

Intervention 1: Intervention group: The oral nutrition begins 24 hours after anastomosis and progresses gradually. (first 24 hours). Intervention 2: Control group: The oral nutrition begins 5 days aft

Sponsors

Qazvin University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 90 Years

Inclusion criteria

Inclusion criteria: All patients undergoing elective digestive surgery (including stomach, small intestine, colon).

Exclusion criteria

Exclusion criteria: certain past medical history such as cirrhosis and rheumatologic disease taking immunosuppressive drugs malnutrition patients

Design outcomes

Primary

MeasureTime frame
Incidence of leaked anastomosis. Timepoint: Daily after operation until discharge. Method of measurement: Physical examination.

Secondary

MeasureTime frame
Incidence of acute edema of the lungs. Timepoint: 24 hours and 5 days after surgery. Method of measurement: Physical examination.;Incidence of infection. Timepoint: 24 hours and 5 days after surgery. Method of measurement: Physical examination.;Incidence of nausea and vomiting. Timepoint: 24 hours and 5 days after surgery. Method of measurement: Physical examination.;Incidence of abdominal pain. Timepoint: 24 hours and 5 days after surgery. Method of measurement: Physical examination.;The amount of received serum. Timepoint: 24 hours and 5 days after surgery. Method of measurement: Liters.;The number of hospitalization. Timepoint: 24 hours and 5 days after surgery. Method of measurement: date.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBahram Shaghaghi

Qazvin University of Medical Sciences

bahram.shaghaghi@gmail.com+98 28 3379 0620

Outcome results

None listed

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