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clinical profile of autonomic dysfunction and mechanical ventilation in Guillian Barre syndrome

Clinical, electrophysiological spectrum and predictors of dysautonomia and successful extubation in Guillian Barre syndrome: a prospective cohort study.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/06/034242
Enrollment
20
Registered
2021-06-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: G00-G99- Diseases of the nervous system

Interventions

Intervention1: nil: nil Control Intervention1: nil: nil

Sponsors

NIL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with GBS, based on clinical, CSF and electro-diagnostic criteria will be included in this study. GBS patients with clinical evidence (defined below) of sympathetic hyperactivity will receive prazosin and titrated as per patientâ??s requirement. clinical evidence of sympathetic hyperactivity includes cold and clammy skin (after ruling out dehydration), presence of hypertension (SBP > 140/90 mmHg) for more than 2 hours with or without pulmonary edema or Labile BP (defined as BP differences of >40mmHg in a single day) or Resting Tachycardia ( > 125 beats per minute) for 2 hours.

Exclusion criteria

Exclusion criteria: Patients with hypo or hyperkalemic paralysis, toxins, porphyria, viral myositis, MND, Cervical myelopathy and CSF cell > 50/mm3 will be excluded. GBS patients with Hypotension (systolic blood pressure < 90 mmHg) and bradycardia ( < 48 beats per minute) will also be excluded.

Design outcomes

Primary

MeasureTime frame
proportion of patients with resolution of sympathetic hyperactivity (dysautonomia defined as 1. SBP/DBP 140/90 mmHg. 2. BP variability 20 mmHg 3. Pulse rate 90/min without bradycardia. 4. resolution of pulmonary edema and other clinical signs of sympathetic over-activityTimepoint: 5 days

Secondary

MeasureTime frame
1. time to resolution of sympathetic over-activity 2. patients developing adverse events to prazosin eg. hypotension, brady cardia etc. 3. disability at 1, 3 and 6 months assessed by Hughes disability scale. 4. proportion of patients succesfully completing 48 hour T-Piece trial. 5. proportion of patients with failed extubation. 6. spectrum of dysautonomia in GBS patients.Timepoint: 6 month

Countries

India

Contacts

Public ContactDr Mritunjai Kumar

all india institute of medical sciences, Rishikesh

mritunjaisingh68@gmail.com9997010096

Outcome results

None listed

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