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effect of vitamin B1 on the level of consciousness

effect of vitamin B1 on the level of consciousness and clinical conditions of patients with decreased level of consciousness hospitalized in intensive care units

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210626051710N1
Enrollment
40
Registered
2022-01-21
Start date
2021-06-22
Completion date
Unknown
Last updated
2022-02-07

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

Conditions

Evaluation of changes in level of consciousness and clinical condition and the effect of vitamin B1.

Interventions

Intervention 1: Intervention group Oral vitamin B1 300 mg plus 30 cc of normal saline is given by gavage once a day (morning). Intervention 2: Control group:30 cc normal saline gavage is given daily (

Sponsors

Khoram-Abad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to No maximum

Inclusion criteria

Inclusion criteria: The Word standard for patients with GCS head injury is equal to or less than 11 Inclusion criteria for patients with stroke have a FOUR score equal to or less than 11 Having a gastric / gastric nasal tube (NG-tube / OGT) Patient with reduced LOC due to brain injury, stroke and other injuries admitted to the ICU No history of head trauma and any pathology and seizures in the past (based on file and family statement) Age limit 15 to 43 years for traumatic patients Do not take certain medications (anticonvulsants, sedatives) before hospitalization Satisfaction of the patient's legal guardian

Exclusion criteria

Exclusion criteria: Have a history of any gastrointestinal bleeding History of any previous seizures Trauma to the mouth and throat and failure to fix the gastric tube

Design outcomes

Primary

MeasureTime frame
Assess the level of consciousness. Timepoint: Daily before intervention and seven days after intervention. Method of measurement: gcs and four scales.;Evaluate the clinical condition. Timepoint: Daily before intervention and seven days after intervention. Method of measurement: Criteria for assessing the clinical status of sofa.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVahid Sepahvandi

Khoram-Abad University of Medical Sciences

sepahvahid8309@gmail.com+98 66 3324 3965

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026