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Pyridostigmine: using a cholinesterase inhibitor to activate the cholinergic anti-inflammatory pathway in patients with CRPS-1 - Pyridostigmine trial

Pyridostigmine: using a cholinesterase inhibitor to activate the cholinergic anti-inflammatory pathway in patients with CRPS-1 - Pyridostigmine trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2009-010758-36-NL
Enrollment
10
Registered
2009-03-02
Start date
2009-05-19
Completion date
Unknown
Last updated
2012-03-19

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

Conditions

Patients with CRPS-1.

Interventions

Trade Name: Mestinon Product Name: Pyridostigmine Product Code: N07AA02 Pharmaceutical Form: Tablet INN or Proposed INN: JP15/USP/INN CAS Number: 101-26-8 Current Sponsor code: D00487 Other descri

Sponsors

VU University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: CRPS-1 patients (Veldman criteria). Age > 18 jaar Standard treatment does not solve the complaints adequately. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: kydney failure other chronic pain syndromes parkinson's disease epilepsy asthma operations on the digestive tract in medical history active malignancy mental retardation

Design outcomes

Primary

MeasureTime frame
Secondary Objective: A secondary objective is an evaluation of possible improvement of clinical well being of the patients treated with Pyridostigmine. Side-effects of Pyridostigmine will be measured on a standardized scale. ;Primary end point(s): Improvement of functional status;Main Objective: The main objective of this trial is to evaluate the effect of Pyridostigmine (cholinesterase inhibitor) on inflammatory signs as pain, temperature, swelling and functional status of the extremity.

Countries

Netherlands

Outcome results

None listed

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