Efficacy of Prophylactic Fluconazole Therapy in Preterm and Very Low Birth Weight Neonates in Preventing Invasive Fungal Infection.

Sponsor
Services Institute of Medical Sciences, Pakistan (Other)
Overall Status
Completed
CT.gov ID
NCT05848492
Collaborator
(none)
110
1
2
6
18.3

Study Details

Study Description

Brief Summary

Invasive fungal infection is detecting candida species in blood, cerebrospinal fluid, or urine. Clinical signs of invasive candidiasis may include lethargy, temperature instability, feeding intolerance, apnea, hypotension, respiratory distress, abdominal distension, and thrombocytopenia. Fungal infection has been associated with an increased risk of retinopathy of prematurity and chronic lung disease. Preterm and low birth weight infants have an immature immune system that predisposes them to infections with bacteria, viruses, and fungi. These infants usually require prolonged admission in the neonatal unit and there is often a need for the administration of broad-spectrum antibiotics which predisposes them to colonization with fungi that may invade to cause systemic disease8. Other risk factors for the development of invasive fungal infection include endotracheal intubation, abdominal surgery, the presence of a central venous catheter, administration of H2 antagonists, and steroids. Infection with Candida species is the third most common cause of bloodstream infection in premature infants. Mortality in preterm infants due to invasive candidiasis is around 20% and can be as high as 50% in infants weighing <1500g at birth. Invasive candidiasis is the second most common infectious cause of death in extremely preterm infants. The present study was conducted to determine the incidence of invasive candidiasis among preterm and very low birth weight infants in our neonatal unit and to evaluate the efficacy of prophylactic fluconazole in preventing invasive fungal infection. Based on the results of the present study institutional guidelines may be designed in our neonatal unit relating to antifungal prophylaxis in preterm and very low birth weight infants.

Condition or Disease Intervention/Treatment Phase
Phase 3

Study Design

Study Type:
Interventional
Actual Enrollment :
110 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Efficacy of Prophylactic Fluconazole Therapy in Preterm and Very Low Birth Weight Neonates in Preventing Invasive Fungal Infection.
Actual Study Start Date :
May 1, 2021
Actual Primary Completion Date :
Oct 31, 2021
Actual Study Completion Date :
Oct 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: Prophylactic Fluconazole

12 mg/Kg loading dose of fluconazole given intravenously followed by 6 mg/Kg every 48 hours till 14 days of life, and then 6 mg/kg/day thereafter, for a total duration of 6 weeks (42 days).

Drug: Fluconazole
Fluconazole will be given for prevention of invasive candidiasis in preterm and very low birthweight babies.

Placebo Comparator: placebo group

Normal Saline 2cc given intravenously

Drug: Saline
0.9% Saline 2cc intravenous will be given to preterm babies in placebo group.

Outcome Measures

Primary Outcome Measures

  1. Invasive candidiases [2 weeks]

    Positive blood, cerebrospinal fluid, or urine culture for candida species will be regarded as invasive candidiasis.

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Hour to 3 Days
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Preterm babies born less than 34 weeks of gestation

  • very low birth weight babies (weighing < 1500 g at birth)

  • Babies <72 hours of age

Exclusion Criteria:
  • Babies >72 hours of life

  • Syndromic babies

  • Babies with suspected metabolic disorders

Contacts and Locations

Locations

Site City State Country Postal Code
1 Services Hospital Lahore Lahore Punjab Pakistan

Sponsors and Collaborators

  • Services Institute of Medical Sciences, Pakistan

Investigators

  • Principal Investigator: M Tauseef Omer, MBBS FCPS Pediatrics, Services Hospital, Lahore

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Muhammad Tauseef Omer, Post-graduate resident, Services Institute of Medical Sciences, Pakistan
ClinicalTrials.gov Identifier:
NCT05848492
Other Study ID Numbers:
  • FluconazolePreterm1
First Posted:
May 8, 2023
Last Update Posted:
May 8, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 8, 2023