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Effect of thiamine on vasopressor requirement in patients with septic shock : A randomized control trial

Effect of thiamine on vasopressor requirement in patients with septic shock

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180310001
Enrollment
62
Registered
2018-03-10
Start date
2018-03-08
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Septic shock Thiamine

Interventions

Thiamine 200 mg + 5%DW 50 mL iv drip in 30 min for 7 days,5%DW 50ml iv drip in 30 min for 7 day
Experimental Drug,Placebo Comparator Other
Thiamine group,Placebo group

Sponsors

Hospital fund
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age over 18 years 2. On vasopressor duration between 1-24 hours 3. Inform consent 4. Suspected infection

Exclusion criteria

Exclusion criteria: 1.recieve thiamine > 100 mg last 24 hours 2. Thiamine allergy or anaphylaxis 3. Cancer that survival rate < 50% at 6 months 4. Who was agnosed cardiac beriberi&#44; peripheral beriberi&#44; korsakoff syndrome&#44; re&#45;feeding

Design outcomes

Primary

MeasureTime frame
Vasopressor free day for 7 days 24 hours Number of day free vasopressor

Secondary

MeasureTime frame
Lactate reduction 24 h 24 hr Variable data,Vasopressor dependency reduction 24 h 24 h Variable data,SOFA score change for 7 days 7 days Variable data,Vasopressor dependency index 7 days Variable data,28 day mortality 28 day Variable data

Countries

Thailand

Contacts

Public ContactSuttasinee Petsakul

Ramathibodi hospital

P.suttasinee@gmail.com0954402296

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026