ociceptive processing in anterior cutaneous nerve entrapment syndrome, a quantitative sensory testing analysis - Nociception in ACNES

niversitair Medisch Centrum Sint Radboud0 个研究点目标入组 70 人开始时间: 待定最近更新: 2024年4月29日

适应症

试验速览

暂无简介。

•1. Patient has been diagnosed with abdominal complaints, matching ACNES:
•i) Patient had a constant site of tenderness that is superficially located with a small (<2cm2) area of maximal tenderness.
•ii) The most intense pain could be localized with the tip of one finger.
•iii) Tenderness increased by abdominal muscle tensing (Carnett*s test).
•2. has been treated (successfully and unsuccessfully) for ACNES.
•3. Patient is at least 18 years old on the day the informed consent form will be signed.
•4. Patient is willing and able to comply with the trial protocol.
•5. Patient is able to speak, read and understand the local language of the investigational site, is familiar with the procedures of the study, and agrees to participate in the study program by giving oral and written informed consent prior to screening evaluations.

•1. Abdominal complaints were due to a condition other than ACNES (e.g. pain related to scar tissue).
•2. Patient has (a history of) another (chronic) pain syndrome that interferes with the interpretation of QST results.
•3. Patient has (a history of) a medical disorder that interferes with the study measurements or may pose a risk for the patient.
•4. Patient does not feel a pinprick test to the lower extremities, due to affected sensory input (e.g. neuropathy as a result of diabetes mellitus).
•5. Female patient is pregnant during the course of the study.

发起方

niversitair Medisch Centrum Sint Radboud