Patients participated in once-a-month 2-hour classes performed by healthcare professionals. VAS pain, WOMAC (Likert Scale) and overall satisfaction with provided medical aid score (0-100 mm VAS scale) ...
Outcome Primary outcomes were visual analogue scale (VAS) pain score change and withdrawal from the study due to lack of efficacy. Results 9 of the patients assessed for eligibility declined to ...
Placebo was sham ultrasound and light application of a non-therapeutic gel, followed by no treatment. Primary outcomes were pain measured by visual analogue scale and patient global change. Secondary ...
The Visual Analogue Scale for Irritable Bowel Syndrome (VAS-IBS) questionnaire was designed to measure the treatment response of symptoms and well-being in patients suffering from IBS. Methods ...
visual analogue pain scale 2, 4, 8, 16, 24 'Mean MAS score' decreased in all botulinum toxin groups at week 8 compared with placebo. Improved VAS score compared with placebo at weeks 8 and 24.
Measurements Outcomes were assessed at baseline and at 3, 6 and 9 months after randomisation. The primary outcome measure was the Impairment level Sum Score—Restricted Version (ISS-RV), consisting of ...
Botulinum toxin (BTX), widely known for its cosmetic and neurological applications, is emerging as a potential treatment for Raynaud’s phenomenon (RP), particularly when secondary to scleroderma.