Evaluation of the Role of N Acetyl Cysteine and Vitamin D in Improving Outcomes After Corrosive Ingestion

• Status: ACTIVE_NOT_RECRUITING
• Trial end date: 2025-12-01

Summary

The goal of this clinical trial is to learn if N acetyl cysteine and vitaminD work to improve outcomes after corrosive ingestion in children.

The main questions it aims to answer are:

Does N acetyl cysteine and vitamin D decrease incidence of strictures after corrosive ingestion in children.

Researchers will compare the effect of N acetyl cysteine and vitamin D in decreasing complication , length of hospital stay and start of complete oral intake Eighty patients were randomly assigned into four groups (1 control and 3 intervention groups 20 patients each)

Group 1 (Control group):

o Patients allocated in this group received the standard treatment protocol only according to PCC-ASUH guidelines

Group 2 (NAC group):

o Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to NAC with loading dose of 150 mg/kg diluted in 200 ml dextrose 5% or saline over 1 hour, followed by a maintenance dose of 50 mg/kg diluted in 500 ml of dextrose 5% or saline over 4 hours then followed by 100 ml/kg diluted in 1000 ml of dextrose 5% or saline over 16 hours

Group 3 (Vitamin D group):

Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to vitamin D in a single intramuscular high-dose (300,000 IU) which was given to all patients regardless patient's age

Group 4 (NAC+Vitamin D group):

Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to both vitamin D and NAC, in the same doses as groups (2 and 3

• Phase: PHASE3

Details

• Lead Sponsor: Ain Shams University
• Treatments: Acetylcysteine; Cholecalciferol; Control Groups