A Pilot Study into the Effect of Topical Menthol for Patients with Neuropathic-Type Pain. - Topical menthol in neuropathic-type pain.

niversity of Edinburgh0 个研究点开始时间: 2008年4月25日最近更新: 2012年3月19日

适应症

试验速览

暂无简介。

•1.Patients with neuropathic-type pain.
•2.Male or female aged 18 years or over at study entry.
•3.Patients whose usual medical team agree to their taking part in the study.
•4.Patients who provide written consent to participation in the study after explanation of the study protocol.
•5.Patients who consent to the relevant parts of their medical notes being accessed by the Research Team.
•6.Patients who, in the opinion of the investigator, are willing and able to attend as an outpatient and are able to complete the various assessments.
•7.Patients need to have the ability to complete questionnaire assessments in English language.
•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

•1.Patients with any contraindication to the use of topical therapy or menthol.
•2.Patients who are confused or suffering from significant psychiatric illness, which would hinder their completion of the study.
•3.Patients whose condition is unstable or rapidly deteriorating, such that they are unlikely to be able to contribute to the study.
•4.Patients with any other medical condition that would confound the objectives of the study.
•5.Patients who would be adversely affected by study participation. This would include those who find completion of the study too burdensome.
•6.Patients who, in the opinion of the Research Team or their usual medical team, would be unable to complete the study protocol for any other reason.
•7.Patients who are unable or refuse to provide written consent to inclusion in the study after explanation of the study protocol.

发起方

niversity of Edinburgh