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Nerve growth factor (mNGF) in preventing and treating critical illness mypahty: a pase 4, randomized, double blinded, placebo-controlled study

Nerve growth factor (mNGF) in preventing and treating critical illness mypahty: a pase 4, randomized, double blinded, placebo-controlled study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IIR-17010724
Enrollment
Unknown
Registered
2017-02-24
Start date
2017-02-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

critical illness myopathy

Interventions

Nerve growth factor group:mouse nerve growth factor
placebo group:placebo

Sponsors

Department of Neurology, Nanfang Hospital, Southern Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Aged = 18 years; 2. Adimmted to neurocritical care unit; 3. Predicted duration of intensive care unit stay = 3 days.

Exclusion criteria

Exclusion criteria: 1. Patients with a certain history of peripheral neuropathy or myopathy, or admitted to the ICU probably because of peripheral neuropathy or myopathy, such as Guilllain-Barre syndrome, polymyositis, myasthenia gravis or botulism; 2. Patients with any chronic diseases related to neuromuscular disease, such as chronic renal failure and chronic alcoholism; 3. Patients unable to perform NCS and EMS examination because of any diseases that injure the upper and the lower limps; 4. Patients unsuitable for NCS examination because of implantation of cardiac pacemaker or defibrillator; 5. Patients in an end-stage or who are critically ill with an expected lifetime < 7 days; 6. Patients with malignant tumor and are under anti-tumor therapy; 7. Patients who are pregnant or under the lactation period; 8. Patients with uncontrolled seizure or with status epileptics and large dose of sedative are required; 9. Patients who have used nerve growth factor from any manufactory after the onset of disease; 10. Patients who do not sign the informed consent; 11. Patients who are regarded unsuitable for this study by the researchers.

Design outcomes

Primary

MeasureTime frame
compound muscle action potential (CMAP) level of median nerve and nervus peroneus communis;

Secondary

MeasureTime frame
incidence of critical illness neuropathy or myopathy;mRS score;duration of mechanical ventilation;length of neurocritical care unit stay;length of hospital stay;incidence of hospital infection;length of antibiotics used;hospital mortality;

Countries

China

Contacts

Public ContactSuyue Pan

Department of Neurology, Nanfang Hospital, Southern Medical University

pansuyue82@126.com+86 13556184981

Outcome results

None listed

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