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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03038503
Other study ID # ID 09-59-14
Secondary ID
Status Recruiting
Phase Phase 3
First received
Last updated
Start date December 2016
Est. completion date December 2018

Study information

Verified date August 2018
Source Ramathibodi Hospital
Contact munthana sundusadee, MD
Phone 66639010178
Email opal_janeway@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The ICU mortality rate of patients with septic shock was still high upto 54.1%.In first 6 hours of resuscitation, the goals of resuscitation in sepsis shock after adequate fluid resuscitation is MAP ≥65 mmHg. In refractory septic shock patient, prolong shock correlate with poor outcome due to multiple organ failure. Alternative vasopressor in septic shock with catecholamine resistance has been studied such as terlipressin, methylene blue

- Terlipressin (TP) mediate vasoconstriction via V1 receptors coupled to phospholipase C, and increases intracellular Ca2+ concentration

- Methylene blue (MB) directly inhibits nitric oxide synthase (NOS) by inhibit the enzyme guanylate cyclase (GC)


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date December 2018
Est. primary completion date December 2018
Accepts healthy volunteers No
Gender All
Age group 15 Years and older
Eligibility Inclusion Criteria:

- Age >15 years old

- Diagnosis septic shock as SCCM/ACCP

- Refractory septic shock defined as hypotension although adequate fluid resuscitate and high dose vasopressor(NE >0.5 mcg/kg/min)

- Concent form

Exclusion Criteria:

- Known case G6PD deficiency

- Acute respiratory distress syndrome (ARDS)

- Hx of drug allergy MB, NE, terlipressin

- Hx of Raynaud's phenomenon, systemic sclerosis, PHT

- Known case coronary heart disease without treatment

- Current drug use serotonin reuptake inhibitors (SSRI), Serotonin and norepinephrine reuptake inhibitors (SNRIs)

- Reject to join project

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Methylene Blue
after defined refractory shock (need NE>0.5 mcg/kg/min) add Methylene blue 1 mg/kg iv drip then 2 hr later drip 0.5 mg/kg/hr*4 hr (intervention add on to standard care)
Terlipressin
after defined refractory shock (need NE>0.5 mcg/kg/min) add terlipressin 1 mg IV then repeated dose 20 min later if unstable BP (intervention add on to standard care)

Locations

Country Name City State
Thailand Ramathibodi hospital Bangkok

Sponsors (1)

Lead Sponsor Collaborator
Ramathibodi Hospital

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary mortality rate 7 days
Primary time to wean of vasopressor through complete weaning off vasopressor, an average of 24 hours
Primary ICU duration through out off indication need ICU care, an average of 7 days
Secondary hemodynamic parameter: Mean arterial pressure (mmHg) mmHg, A-line monitoring every 30 min after start protocol up to 6 hr then every 1 hr up to 24 hours
Secondary hemodynamic parameter: lactate (mmol/l) mmol/l every 2 hr until 6 hr then every 4 hr until wean off vasopressor up to 24 hours
Secondary hemodynamic parameter: urine output (ml) ml every 2 hr until wean off vasopressor up to 24 hours
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