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Efficacy of Melatonin in Patients With Severe Sepsis or Septic Shock

Primary Purpose

Severe Sepsis, Septic Shock

Status
Unknown status
Phase
Phase 3
Locations
Spain
Study Type
Interventional
Intervention
Melatonin
Sponsored by
Aragon Institute of Health Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Severe Sepsis focused on measuring Sepsis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients (males and females) over 18 years who meet the diagnostic criteria for severe sepsis or septic shock secondary to community-acquired pneumonia or hospital and or intra-abdominal infection

Exclusion Criteria:

  • Patient with more than 24 hours from the first documentation of organ dysfunction

Sites / Locations

  • Hospital Clínico Universitario Lozano Blesa

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Control

Melatonin

Arm Description

saline every 12 hours for 28 days

Oral 30mg/12hours melatonin 28 days

Outcomes

Primary Outcome Measures

Mortality
Mortality at 28 days of study entry.
Clinical evolution parameters
Days of mechanical ventilation. Days with vasoactive drugs. Days with hemodialysis or hemofiltration. Superinfection of organs other than the initial cause of the sepsis. Progression to other organs fail after starting the treatment.

Secondary Outcome Measures

Clinical evolution
clinical - analytical parameters relative to the sepsis
Oxidative-nitrosative parameters
Melatonin plasmatic levels Quantification of malonyldialdehyde and 4-hydroxynonenal Protein carbonyl content Nitrites Erythrocyte membrane fluidity Superoxide dismutase, catalase, glutathione reductase and glutathione peroxidase activity
Inflammatory parameters
Interleukins-1,2,4,5, 6, 7,8,10,12,13, IFN-γ; TNF-α and GM-CSF
Acute phase proteins
PCR, haptoglobin, Apo A-I, α1-GPA and ITIH4
Immune parameters
Lymphocytes T, B, NK, T CD4, and T CD8, and immunoglobulins
Endocrine parameters
Cortisol, aldosterone, ACTH, ADH, insulin, glucagon and 25-hydroxyvitamin D3

Full Information

First Posted
May 17, 2013
Last Updated
May 17, 2013
Sponsor
Aragon Institute of Health Sciences
Collaborators
Ministerio de Sanidad, Servicios Sociales e Igualdad
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1. Study Identification

Unique Protocol Identification Number
NCT01858909
Brief Title
Efficacy of Melatonin in Patients With Severe Sepsis or Septic Shock
Official Title
Phase III, Prospective, Randomized, Double-blind Clinical Trial to Evaluate the Efficacy of Melatonin in Patients With Severe Sepsis or Septic Shock
Study Type
Interventional

2. Study Status

Record Verification Date
May 2013
Overall Recruitment Status
Unknown status
Study Start Date
May 2013 (undefined)
Primary Completion Date
December 2013 (Anticipated)
Study Completion Date
December 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Aragon Institute of Health Sciences
Collaborators
Ministerio de Sanidad, Servicios Sociales e Igualdad

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
OBJECTIVES. To establish the therapeutic efficiency of melatonin in adult patients with severe sepsis and septic shock. Specifically: To evaluate the survival to 28 days of mechanical assisted ventilation, days with vasoactive drugs, need of hemodialysis-hemofiltration, superinfection and evolution towards the failure of other organs. To evaluate, waiting for reduction under the influence of the treatment with melatonin, : clinical - analytical parameters of sepsis; levels of cytokines; oxidative and nitrosative stress; acute-phase proteins (APP), specially of the ITIH4; immune response; endocrine response. METHODOLOGY. Patients will be randomized in two groups, n = 55 in each group: 1) treatment with melatonin 30mg/12 hours 28 days; 2) placebo. Determinations: a) clinical - analytical parameters relative to the sepsis; b) melatonin plasmatic levels; c) quantification of malonyldialdehyde and 4-hydroxynonenal, protein carbonyl content, nitrites, erythrocyte membrane fluidity, and superoxide dismutase, catalase, glutathione reductase and glutathione peroxidase activity; d) Interleukins-1,2,4,5, 6, 7,8,10,12,13, IFN-γ; TNF-α and GM-CSF; e) acute-phase proteins: PCR, haptoglobin, Apo A-I, α1-GPA and ITIH4; f) lymphocytes T, B, NK, T CD4, and T CD8, and immunoglobulins; g) cortisol, aldosterone, ACTH, ADH, insulin, glucagon and 25-hydroxyvitamin D3. Data will be analyzed following a prospectively define plan and by intention-to-treat (ITT) analysis.
Detailed Description
This study will be done in the Hospital Clinico Lozano Blesa (Zaragoza, Spain), promoted by the Health Science Aragon Institute and its principal investigator is F. Agustín García Gil (Surgical Service). It will start in April-May 2013 and will finish 12 months later approximately. The study sponsor is I+CS (Aragon Institute of Health Sciences).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe Sepsis, Septic Shock
Keywords
Sepsis

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
110 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
saline every 12 hours for 28 days
Arm Title
Melatonin
Arm Type
Experimental
Arm Description
Oral 30mg/12hours melatonin 28 days
Intervention Type
Drug
Intervention Name(s)
Melatonin
Other Intervention Name(s)
Liquid 1 mg/mL Melatonin
Intervention Description
Administration via oral or via a nasogastric tube followed by 20mL saline
Primary Outcome Measure Information:
Title
Mortality
Description
Mortality at 28 days of study entry.
Time Frame
1 month
Title
Clinical evolution parameters
Description
Days of mechanical ventilation. Days with vasoactive drugs. Days with hemodialysis or hemofiltration. Superinfection of organs other than the initial cause of the sepsis. Progression to other organs fail after starting the treatment.
Time Frame
1 month
Secondary Outcome Measure Information:
Title
Clinical evolution
Description
clinical - analytical parameters relative to the sepsis
Time Frame
1 month
Title
Oxidative-nitrosative parameters
Description
Melatonin plasmatic levels Quantification of malonyldialdehyde and 4-hydroxynonenal Protein carbonyl content Nitrites Erythrocyte membrane fluidity Superoxide dismutase, catalase, glutathione reductase and glutathione peroxidase activity
Time Frame
1 month
Title
Inflammatory parameters
Description
Interleukins-1,2,4,5, 6, 7,8,10,12,13, IFN-γ; TNF-α and GM-CSF
Time Frame
1 month
Title
Acute phase proteins
Description
PCR, haptoglobin, Apo A-I, α1-GPA and ITIH4
Time Frame
1 month
Title
Immune parameters
Description
Lymphocytes T, B, NK, T CD4, and T CD8, and immunoglobulins
Time Frame
1 month
Title
Endocrine parameters
Description
Cortisol, aldosterone, ACTH, ADH, insulin, glucagon and 25-hydroxyvitamin D3
Time Frame
1 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients (males and females) over 18 years who meet the diagnostic criteria for severe sepsis or septic shock secondary to community-acquired pneumonia or hospital and or intra-abdominal infection Exclusion Criteria: Patient with more than 24 hours from the first documentation of organ dysfunction
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Francisco A García-Gil, Physician
Organizational Affiliation
Hospital Clínico Universitario Lozano Blesa
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Clínico Universitario Lozano Blesa
City
Zaragoza
ZIP/Postal Code
50009
Country
Spain

12. IPD Sharing Statement

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Efficacy of Melatonin in Patients With Severe Sepsis or Septic Shock

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