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| Sponsor: | University of Malawi College of Medicine |
|---|---|
| Information provided by: | University of Malawi College of Medicine |
| ClinicalTrials.gov Identifier: | NCT00619203 |
Purpose
Bacterial meningitis remains a significant cause of morbidity and mortality in children, especially in countries with limited resources. Efforts to improve the grim outcome have included altering the first line antibiotic therapy, controlling seizures and managing fluids more carefully. Adjuvant therapy of steroids has been used with limited success in children in the West and with no proven value in Malawi and other resource constrained settings. Glycerol has been used to reduce brain oedema in neurosurgery and it has recently been shown to reduce morbidity in childhood meningitis in South America. Paracetamol in a high dosage has been shown to reduce inflammation and cytokine levels in septicaemia with improved outcomes in adults.
In Malawi the investigators have tried adjuvant steroids with no improvement in outcome of childhood meningitis. They have recently concluded a study of ceftriaxone which has shown no improvement in mortality though there is less hearing loss than with chloramphenicol and benzyl penicillin.
Following the encouraging results of the Childhood South American Study it is important to assess the use of adjuvant glycerol in children in the investigators' setting. Paracetamol is routinely used in meningitis because of the accompanying fever and headache. This is an opportunity to study its place as adjuvant therapy more carefully than has previously been done.
The investigators propose a prospective, randomized, double blind 2 by 2 factorial designed study to assess the advantage of ceftriaxone (antibiotic) given with paracetamol and glycerol in combination, singly or with neither adjuvant therapy in childhood bacterial meningitis.
| Condition | Intervention | Phase |
|---|---|---|
|
Bacterial Meningitis |
Drug: Glycerol and paracetamol Drug: Paracetamol Drug: Placebo Drug: Paracetamol and glycerol Drug: Glycerol |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Factorial Assignment, Efficacy Study |
| Official Title: | Oral Glycerol and High-Dose Rectal Paracetamol to Improve the Prognosis of Childhood Bacterial Meningitis - A Prospective, Randomized, and Double-Blind Clinical Study Using a Two-by-Two Factorial Design |
| Estimated Enrollment: | 750 |
| Study Start Date: | March 2008 |
| Estimated Study Completion Date: | January 2012 |
| Estimated Primary Completion Date: | March 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
A: Active Comparator
Two active ingredients
|
Drug: Glycerol and paracetamol
glycerol by mouth (po) 1.5ml/kg max 25 ml/dose x 6 hourly x 8 doses paracetamol PR 35 mg/kg first dose, then 20 mg/kg 6 hourly x 7 35 mg/kg po first dose, then 20 mg/kg 6 hourly x 7 paracetamol 1.5 ml/kg max 25 ml/dose 6 hourly x 8 doses |
|
B: Active Comparator
One active ingredient
|
Drug: Paracetamol
paracetamol 35 mg/kg first dose, then 20 mg/kg 6 hourly x 7 doses
Drug: Glycerol
glycerol 1.5 ml/kg /dose 6 hourly x 8 max dose = 25ml
|
|
C: Active Comparator
One (other) active ingredient
|
Drug: Paracetamol
paracetamol po 35 mg/kg first dose, then 20 mg/kg 6 hourly x 7 doses plus placebo suppository
Drug: Paracetamol
po 35 mg/kg first dose, then 20 mg/kg 6 hourly x 7 doses plus placebo suppository
|
| D: Placebo Comparator |
Drug: Placebo
2 placebos, one po, one suppository
|
Hide Detailed DescriptionBacterial meningitis (BM) is a major cause of morbidity and death in the developing world. Hib and pneumococcal conjugate vaccines have the potential to prevent meningitis but neither vaccine is available in many countries with limited resources. New (and expensive) antimicrobials have done little to improve the prognosis. A background of HIV infection in many parts of the world adds to the grim prognosis of childhood BM. Adjuvant dexamethasone has gained much attention, because of its effects in damping the host's inflammatory response in childhood BM. However, little or no clinical benefit has been observed in several studies. Most importantly, the first sufficiently powered study in Malawi found no benefit at all. Another sufficiently powered (N=654) study on childhood BM, recently completed in Latin America, showed little benefit of dexamethasone even in Hib meningitis but did show benefit from adjuvant oral glycerol.
It is not known how glycerol works, and there is probably more than one mechanism. One-third of children with bacterial meningitis suffer from significantly reduced cerebral blood flow caused by intracranial oedema. Glycerol slightly increases serum osmolality, and this small change may improve rheology and enhance cerebral circulation, perhaps by increasing perfusion pressure. Thus, extravascularization of water and hidden hypovolemia is improved. Osmotic diuresis is of less importance, because urinary output does not increase with these doses (6 ml/kg/day) of glycerol. A gradient between the body compartments would require an intact or nearly intact blood brain barrier (BBB), and that is not the case in BM. Glycerol is also a scavenger of free oxygen radicals. This activity may alleviate the inflammation characteristic of BM.
Paracetamol is used widely as an antipyretic, analgesic, and anti inflammatory agent. It is effective, safe, inexpensive, and available as a syrup, tablet, suppository and injection; it suits all ages. The effect is dose-dependent. There are very few contraindications, eg allergy. The mechanisms are not well understood, but NSAIDs dampen inflammatory reactions other than those mediated by inhibition of arachidonic acid metabolism. There are differences between paracetamol and other NSAIDs: paracetamol inhibits the centrally located COX 3 and NMDA receptors, other NSAIDs inhibit COX 2 receptors in periphery. These mechanisms may partly explain the different results in patient outcome. In a retrospective analysis of 809 adult patients with bacteremia in Finland, those who received paracetamol had a better survival rate than those treated with other NSAIDs or salicylate.
A prospective clinical trial on childhood BM in which the value of glycerol is reviewed, and the potential of paracetamol is examined is warranted. Both adjuvants aim to improve the poor prognosis of this disease.
Objectives
A Prospective, Randomized, and Double-Blind Clinical Study Using a Two-by-Two Factorial Design to answer two questions:
The primary end points are:
Various patient characteristics are taken into account as covariates, eg severity of illness, age, aetiological agent, haemoglobin level, HIV status and presence of malaria co-infection.
The secondary end points are
1. audiological or neurological sequelae (according to the Denver-II developmental screening test).
Eligibility| Ages Eligible for Study: | 2 Months to 15 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Malawi | |
| College of Medicine, Queen Elizabeth Central Hospital | Recruiting |
| Blantyre, Malawi, 3 | |
| Contact: Elizabeth M Molyneux, FRCPCH 265 1 873 198 emolyneux@malawi.net | |
| Contact: E Borgstein, FRCS 265 1871 911 eborgstein@medcol.mw | |
| Principal Investigator: Elizabeth M Molyneux, FRCPCH | |
More Information
| Responsible Party: | College of Medicine, Malawi ( Prof. Elizabeth Molyneux ) |
| Study ID Numbers: | P.03/07/499 |
| Study First Received: | February 7, 2008 |
| Last Updated: | June 16, 2008 |
| ClinicalTrials.gov Identifier: | NCT00619203 History of Changes |
| Health Authority: | Malawi: National Health Sciences Research Committee |
|
Bacterial meningitis glycerol high dose paracetamol children |
|
Bacterial Infections Physiological Effects of Drugs Meningitis, Bacterial Nervous System Diseases Central Nervous System Diseases Protective Agents Cryoprotective Agents Pharmacologic Actions Meningitis Glycerol |
Central Nervous System Infections Analgesics, Non-Narcotic Sensory System Agents Therapeutic Uses Central Nervous System Bacterial Infections Analgesics Peripheral Nervous System Agents Central Nervous System Agents Acetaminophen |
