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Midodrine in Septic Shock

Evaluation of Midodrine Effect on Lactate Clearance in Patients with Septic Shock

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100228003449N25
Enrollment
42
Registered
2019-09-03
Start date
2019-09-23
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Sepsis and septic shock. Sepsis, unspecified organism

Interventions

Intervention 1: Intervention group: Patients in this group will receive midodrine tablet 10 mg three times a day (Takeda Pharmaceutical Company., Austria) concomitant with the standard care of septic

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with age over 18 years old Patients with diagnosis of septic shock (need for intravenous vasopressor to maintain MAP= 65 mmHg Serum lactate level over 18 mg/dL

Exclusion criteria

Exclusion criteria: ?More than 24 hours of septic shock diagnosis Chronic kidney disease (eGFR < 30 ml/min) Urinary disorders and neurogenic bladder Heart failure (Ejection Fraaction < 50%) Moderate to severe valvular diseases Pulmonary hypertension and PAP= 45 mmHg Peripheral arterial disease Scleroderma Heart rate below 60 beats per minute Recent history of midodrine use

Design outcomes

Primary

MeasureTime frame
Serum lactate. Timepoint: Two times a day (up to when serum lactate level set to <18 mg/dL). Method of measurement: Colorimetric.

Secondary

MeasureTime frame
Lactate clearance. Timepoint: Daily. Method of measurement: Calculation (Comparing two daily serum lactate levels).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHossein Khalili

Tehran University of Medical Sciences

khalilih@tums.ac.ir+98 21 6658 1598

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 15, 2026