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OpenTrials
Completed

NCT Number: NCT05680428

Early Feeding Versus Conventional Feeding

The goal of this clinical trial is to compare early feeding vs conventional feeding after stoma reversal. The main question it aims to answer are:

• whether it is beneficial to start oral feeding within 12hrs after stoma reversal

Participants will be randomly assigned two groups either early feeding or conventional group

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Key information

Conditions

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

DHQ

Mardan, Kpk, 25300, Pakistan

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • having ileostomy
  • no peritonitis
  • intestinal obstruction

Exclusion criteria

  • uncontrolled diabetes
  • uncontrolled hypertension
  • sepsis

Treatment and study plan

Early feeding

Other

oral feeding within 12hours after stoma reversal

conventional feeding

Procedure

oral feeding after 48hours of NBM after stoma reversal

Primary outcomes

  1. To evaluate the outcome of early versus conventional oral feeding in stoma reversal in terms of postoperative ileus

    Time frame: 5days

    comparison of post-op anastomotic leakage hospital stay wound infection

Sponsors and collaborators

Lead sponsor

DHQ mardan

Other

Collaborators

  • DHQ HOSPITAL MARDAN

Registry information

Official study title

Effectiveness of Early Feeding Versus Conventional Feeding After Stoma Reversal in Adult Surgical Surgical Practices

Important dates

Study start
2020
Primary completion
2022
Study completion
2022
First posted
Jan 11, 2023
Registry last updated
Jan 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.