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Efficacy of gamma globulin combined with methylprednisolone in the treatment of patients with TRF-GBS or progressive GBS

Efficacy of gamma globulin combined with methylprednisolone in the treatment of patients with TRF-GBS or progressive GBS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900028168
Enrollment
Unknown
Registered
2019-12-14
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

Guillian-Barre syndrome

Interventions

Two groups:Methylprednisolone versus IVIG

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 100 Years

Inclusion criteria

Inclusion criteria: 1. Combined with Asbury or Cornblath diagnostic criteria, and refer to the diagnostic criteria of China 2010 guidelines, the diagnosis as GBS; 2. TRF-GBS or progressive GBS patients with symptomatic fluctuations at the same time, TRF-GBS diagnostic criteria reference: 1991 Kleyweg diagnostic criteria, the specific manifestations are as follows: (1) After GBIG patients were treated with IVIG or PE, the Hughes score of the patients improved by at least 1 point compared with before treatment, and then the Hughes score increased within at least 1 point within 8 weeks of onset, or the condition was stable after the treatment was greater than 1 point. Hughes score appeared at least 1 point worse than before; (2) Patients with GBS who have undergone IVIG or PE treatment; patients who have improved their Hughes score by less than 1 point and continue to progress.

Exclusion criteria

Exclusion criteria: 1. Patients who give up examination and treatment within 5 days of admission; 2. Patients with acute or chronic peripheral neuropathy due to other reasons cannot be excluded; 3. Patients who refuse to use IVIG or PE within 2 weeks of onset, or have been treated with hormones; 4. Have been retreated with IVIG, PE or hormones in two weeks after onset.

Design outcomes

Primary

MeasureTime frame
Hughes score;

Countries

China

Contacts

Public ContactZhou Yanxia

Shenzhen Guangdong Province, the Second People's Hospital

xiaxue159@163.com+86 18928488136

Outcome results

None listed

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