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Necrotizing Soft Tissue InfectionPhase 2INSTINCTNCT02111161

Immunoglobulin for Necrotizing Soft Tissue Infections: a Randomised Controlled Trial

A Phase 2 study testing IVIG (Privigen) and Saline 0.9% in people with Necrotizing Soft Tissue Infection and Necrotizing Fasciitis, run by Anders Perner at 1 site in Denmark.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to estimate the effect of intravenous polyspecific immunoglobulin G (IVIG) compared with placebo (saline) on the patient-reported outcome measure Physical Component Summary Score (PCS) of the SF-36 in patients with necrotizing soft tissue infections (NSTI). Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
IVIG (Privigen) and Saline 0.9%
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
100 participants
Where
1 siteDenmark
Study dates
Apr 2014to Sep 2016
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Necrotizing soft tissue infection (NSTI) based on surgical findings
  • Age >18 years
  • Admitted to or planned to be admitted to the ICU at Rigshospitalet (RH)

Who cannot join

  • >48 hour from the primary diagnosis to arrival at RH
  • More than one dose of IVIG given within current admission
  • Known hypersensitivity to IVIG
  • Hyperprolinaemia (obtained from hospital notes)
  • Pregnancy or breast feeding

Trial locations and contacts

1 site in 1 country.

Denmark1 site
  • Dept. of Intensive Care 4131, Copenhagen University Hospital, Rigshospitalet

    Copenhagen, Danmark, 2100

Other trials in Denmark

About this study

The purpose of this study is to estimate the effect of intravenous polyspecific immunoglobulin G (IVIG) compared with placebo (saline) on the patient-reported outcome measure Physical Component Summary Score (PCS) of the SF-36 in patients with necrotizing soft tissue infections (NSTI).

Read the detailed description

Patients with necrotizing soft tissue infections (NSTI) receive intravenous polyspecific immunoglobulin G (IVIG) as part of the standard treatment at Rigshospitalet. The current evidence available does not support neither the use of IVIG, nor omitting it, as adjuvant treatment of NSTI. With this trial the investigators will estimate the effects of IVIG on a patient-reported outcome and other important outcomes in patients with NSTI

Design A randomized, double-blinded, clinical trial where patients are randomly assigned 1:1 to receive either IVIG or an equal volume of 0.9% saline.

Location A single centre trial conducted at Dept. of Intensive Care 4131, Copenhagen University Hospital, Rigshospitalet.

Randomisation Randomisation will be stratified according to primary presentation of NSTI on the extremities/head/neck (yes/no) as streptococci mainly affect these anatomical sites. Two randomisation lists, with varying block size, are generated. Two separate boxes contain sequentially numbered, opaque, sealed envelopes (SNOSE). Two people independent of the trial will generate the envelopes following the randomisation lists and will document that the envelopes are concordant with the randomisation lists. Staff at trial site will have access to the boxes around the clock, and will draw an envelope containing a patient randomisation- and medicine log document assigned either "Privigen" or "Saline" from one of the two boxes.

Intervention Trial medicine is given when the patient arrives at the ICU and the following two consecutive days. Alternatively, the first dose of trial medicine will be given in the operating theatre.The trial medicine will consist of either IVIG 25 g/day (250 ml) (Privigen, CSL Behring) or an equal volume of 0.9% saline. The dosage of IVIG is 25g/day for three consecutive days for all patients, which is according to the clinical protocol at Rigshospitalet. The treatment will be given according to the clinical protocol for Privigen at Rigshospitalet. The treating clinicians will decide all other interventions.

Blinding The trial medicine will be prepared in the ICU at the time of arrival of the patient and the following two consecutive days by an ICU nurse not otherwise involved in the care of the trial patient and is supervised by another staff member who as well is not involved in the care of the patient. Privigen has a slight yellowish appearance whereas saline is clear. Furthermore, Privigen is produced in bottles of 50 and 100 ml, respectively. A bottle of Privigen will be packed with a bag of saline, containing a corresponding number of millilitres, in a black plastic bag and sealed with a plastic strip. An orange, transparent infusion set (B. Braun, ref. 8700127SP) is inserted into either the Privigen bottle or the bag containing saline, dependent on whether the patient has been allocated to active treatment or placebo. The orange colour masks the fluid colour while allowing air bubbles to be seen. A piece of non-transparent tape will mask the drip chamber making it impossible to see the frothing of Privigen. For each of the three dosages of trial medicine, three bags are prepared, containing 100 ml, 100 ml and 50 ml respectively. The bag will be marked with an etiquette containing the patient number. If unblinding is necessary, this is easily done by looking in the envelope with the same patient number.

Medicine score The trial medicine batch number will be noted on the patient randomisation- and medicine log document by the ICU nurse preparing the trial medicine. The attending physician will prescribe "trial medicine" in the electronic medication file (CIS 3.9.1, Daintel).

Subgroup Analysis Presumed Streptococcal Infection A subgroup analysis will be performed on patients with primary presentation of NSTI on the extremities, neck or head as these are more likely to be streptococcal infections, in which the effects of IVIG may be different.

Data Registration Data will be entered into the electronically, web-based case report form (eCRF) from patient notes by trial personnel. The eCRF is specifically designed for this purpose.

Safety

Patients will be withdrawn from the trial protocol if the following occurs:

  • SARs or SUSARs Patients withdrawn from the trial for the above mentioned reasons will receive the standard protocol treatment for NSTI with the exception of IVIG.

During the trial, Sponsor will send yearly reports on the occurrence of SARs to the Danish Health and Medicines Authority and Regional Ethics Committee.

Suspected Unexpected Serious Adverse Reactions Suspected unexpected serious adverse reactions (SUSARs) will be defined as serious adverse reactions not described in the summary of product characteristics (SPC) for Privigen (no serious adverse reactions are described for 0.9% saline). Sponsor will report any SUSARs within 7 days to the Danish Health and Medicines Authority via Eudravigilance Clinical Trials Module, to the Regional Ethics Committee and to CSL Behring. During the trial, investigator will send yearly reports on the occurrence of SUSARs to the Danish Health and Medicines Authority and the Regional Ethics Committees.

Adverse Events and Serious Adverse Events Adverse events (AEs) and serious adverse events (SAEs) will not be recorded as an entity because the majority of ICU patients will experience several SAEs during their critical illness. In addition, most SAEs will be captured in the secondary outcome measures (SOFA scores and bleeding).

Termination of Trial The trial will be terminated prematurely in the case that new, definite information regarding the use of IVIG in patients with NSTI arises.

Sample Size Estimation 50 subjects in each group are needed to detect a difference of 7 points in PCS of SF-36 based on an expected score of 42 (SD 11) in the control group (data from our own follow-up studies), for a power of 80% and a two-tailed significance level of 0.05, and an expected 1-year mortality rate of 20%.

Statistical Methods Analysis will be by intention-to-treat comparing PCS of SF-36 in the two groups after six months by chi-squared test and multiple logistic regression analysis using unadjusted analyses and analyses adjusted for patient variables (SAPS II and SOFA score in the 24 h prior to randomisation).

Patients Included In Final Statistical Analysis Patients who are withdrawn from the trial protocol will be followed up and analysed as the remaining patients. Patients who are transferred to another ICU will be followed up for the primary outcome measure. Patients who are withdrawn will not be replaced by new patients, with the exception of the specific case, where the patient demands deletion of all registered data.

Accountability Procedure for Missing Data Imputation will be used if missingness >5%.

Interim Analysis An interim analysis will not be performed as analyses of a sample size below the planned 100 patients are less meaningful for those outcomes that are of relevance (mortality and SARs).

Monitoring

We will perform Good Clinical Practice (GCP)-monitoring according to a predefined monitoring plan including the following issues:

  • Initiation visit
  • For all patients: Documented informed consent
  • Inclusion and exclusion criteria
  • Documented delivery or non-delivery in the eCRF of the intervention according to the protocol compared with source data being patients' hospital records
  • Termination visit: Primary outcome

Data Handling and Record Keeping Data will be handled according to the National Data Protection Agency, and is protected by the national law "Loven om behandling af personoplysninger" and "Sundhedsloven". All original records (incl. consent forms, eCRFs, and relevant correspondences) will be archived at trial site for 15 years. The clean electronic trial database file will be delivered to the Danish Data Archive and maintained for 15 years and anonymised if requested by the authorities.

Quality Control and Quality Assurance The subinvestigator will be responsible for preparing the research nurses and other trial site personnel before the initiation of the trial. This education will be continuously documented.

Monitoring of the Intervention Groups Day-to-day monitoring of the eCRF will be done by persons delegated to this specific task.

Ethics The trial will adhere to the Helsinki Declaration and Danish law. Inclusion will start after approval by the Regional Ethics Committee, the Danish Health and Medicines Authority and the National Data Protection Agency (via the Joint Notification System of The Capital Region of Denmark - Region Hovedstaden) and trial registration at www.clinicaltrials.gov.

Being tested
IVIG (Privigen), Saline 0.9%
Keywords
Randomised controlled trial (RCT), Immunoglobulin, Patient Reported Outcome, Health-Related Quality of Life, Short Form-36 (SF-36)
Medical subject headings
Fasciitis, Necrotizing, Gas Gangrene, Fournier Gangrene

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • IVIG (Privigen)Drug

    Also called Privigen, Immunoglobulin G

    Three doses of 25 g IVIG (250 ml)

  • Saline 0.9%Drug

    Also called NaCl

    Three doses of Saline 0.9% (250 ml)

Study groups in NCT02111161
Study groupRoleWhat they receive
IVIG (Privigen)Active comparatorIntravenous polyspecific immunoglobulin G (Privigen). Dosage: 25 g/day (250 ml) for three consecutive days
Receives: Drug: IVIG (Privigen)
Saline 0.9%Placebo comparator0.9% saline for Intravenous administration. Dosage: 250 ml for three consecutive days.
Receives: Drug: Saline 0.9%

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Physical Component Summary Score (PCS) of Short-Form 36 (SF-36)

    Measured: Six months after randomisation

Secondary outcomes (11)
  1. Mortality

    Measured: 28, 90 and 180 days

  2. Time to resolution of shock

    Maintenance of a systolic blood pressure of at least 90 mmHg without vasopressor support for 24 hours

    Measured: During ICU admission (expected average of 8 days)

  3. Severe bleeding

    Clinical bleeding and use of 3 units of red blood cells (RBCs) within 24 hours at any time in the ICU

    Measured: During ICU admission (expected average of 8 days)

  4. Any bleeding in the ICU

    Measured: During ICU admission (expected average of 8 days)

  5. Use of blood products

    Total volumes during the ICU admission

    Measured: During ICU admission

  6. SOFA scores (AUC), excluding the Glasgow Coma Score (GCS) score

    Measured: Day 1-7

  7. Use of renal replcement therapy (RRT), ventilation and vasopressor in the ICU

    Measured: During ICU admission (expected average of 8 days)

  8. Days alive off life support in the 90 days after randomisation

    Measured: 90 days after randomisation

  9. Days alive and out of hospital in the 180 day follow-up period

    Measured: 180 day follow-up period

  10. Amputation, any location

    Measured: Within 180 days

  11. Serious Adverse Reactions (SARs) in the ICU

    • Allergic reactions
    • Haemolytic anaemia
    • Aseptic meningitis syndrome
    • Thrombus
    • Transmittable agents
    • Acute kidney injury

    Measured: During ICU admission (expected average of 8 days)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Apr 2014 (estimated)
  2. Study startApr 2014
  3. Primary completionSep 2016
  4. Study completionSep 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
100 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02111161
Sponsor's protocol ID
RH4131-03
Acronym
INSTINCT
Status last verified
Sep 2016
First submitted
3 Apr 2014
Last updated
30 Sep 2016
Results posted
No
Data monitoring committee
No

Publications

  • Bergsten H, Madsen MB, Bergey F, Hyldegaard O, Skrede S, Arnell P, Oppegaard O, Itzek A, Perner A, Svensson M, Norrby-Teglund A; INFECT Study Group. Correlation Between Immunoglobulin Dose Administered and Plasma Neutralization of Streptococcal Superantigens in Patients With Necrotizing Soft Tissue Infections. Clin Infect Dis. 2020 Oct 23;71(7):1772-1775. doi: 10.1093/cid/ciaa022.

    PubMed 31916575
  • Madsen MB, Hjortrup PB, Hansen MB, Lange T, Norrby-Teglund A, Hyldegaard O, Perner A. Immunoglobulin G for patients with necrotising soft tissue infection (INSTINCT): a randomised, blinded, placebo-controlled trial. Intensive Care Med. 2017 Nov;43(11):1585-1593. doi: 10.1007/s00134-017-4786-0. Epub 2017 Apr 18.

    PubMed 28421246
  • Madsen MB, Lange T, Hjortrup PB, Perner A. Immunoglobulin for necrotising soft tissue infections (INSTINCT): protocol for a randomised trial. Dan Med J. 2016 Jul;63(7):A5250.

    PubMed 27399982

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing IVIG (Privigen) and Saline 0.9% in people with Necrotizing Soft Tissue Infection and Necrotizing Fasciitis, run by Anders Perner at 1 site in Denmark.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 30 Sep 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Physical Component Summary Score (PCS) of Short-Form 36 (SF-36) (time frame: Six months after randomisation). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02111161, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Sep 2016.

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