Actively Recruiting

Phase Not Applicable
Age: 6Years - 14Years
All Genders
NCT07016919

Early vs Conventional Enteral Nutrition After Uncomplicated Paediatric Open Appendectomy

Led by Shaikh Zayed Hospital, Lahore · Updated on 2025-06-15

88

Participants Needed

1

Research Sites

27 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This clinical trial is conducted to see if after surgery of appendix(open appendectomy) in children giving oral nutrition within 6hours of surgery instead of older method of starting oral nutrition after 24hours of surgery improves the outcome or not which is the length of hospital stay(from the day of surgery until discharge) and to look for complications associated with oral nutrition (nausea, vomiting, abdominal distension, diarrhea) as well as return of bowel activity after surgery that is passage of flatus(gas) and stool.Participants after taking informed consent are enrolled in two groups,group A in which oral nutrition is started in 6hours and group B in which oral nutrition is started after 24hours of surgery and then see for the outcome during hospital stay until 1week after discharge on follow up.

CONDITIONS

Official Title

Early vs Conventional Enteral Nutrition After Uncomplicated Paediatric Open Appendectomy

Who Can Participate

Age: 6Years - 14Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 6 and 14 years
  • Male or female
  • Diagnosed with uncomplicated appendicitis (no perforation or gangrene)
  • Underwent open appendectomy
  • ASA grade 1 only
  • Willing to participate and attend follow-up visits
Not Eligible

You will not qualify if you...

  • Having any underlying health problems or organ dysfunction such as kidney, gastrointestinal, respiratory, or congenital heart disease
  • Severe malnutrition or obesity with BMI greater than 25
  • Previous surgical history related to the gut
  • Presence of any malignancy
  • Surgery lasting longer than 3 hours (anesthesia time)
  • Complicated appendicitis (gangrene, perforation, or intra-abdominal abscess)
  • Postoperative shock
  • Ongoing infection
  • Gastrointestinal dysfunction like acid reflux or obstruction

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Shaikh Zayed federal postgraduate medical institute Lahore

Lahore, Punjab Province, Pakistan

Actively Recruiting

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Research Team

D

Dr Noor Ulain

CONTACT

D

Dr Muhammad Sooban Qamar

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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