Clinical Evidence

Study Two

Efficacy of Gelclair® in reducing pain in patients with oral lesions − preliminary findings from an open pilot study

Innocenti M, Moscatelli G, Lopez S.

Pain Symptom Manage 2002; 24(5): 456−457.

Patients' Response

Study Outline

Thirty patients with painful lesions of the mouth and oropharynx (caused by various diseases) were evaluated for short term (5−7 hours) and medium term (7−10 days) effects of Gelclair® on the severity of pain on swallowing and eating.

Results

The significant reduction was observed with the short term not medium term. The results are encouraging but not conclusive. In this 10 day trial, results indicated that Gelclair® rapidly and effectively reduces pain associated with oral lesions (e.g. oral mucositis), and can improve ability to eat and drink, with continued use.

Reporting of side effects

Medical device adverse incidents should be reported to the MHRA. Reporting information can be found at https://yellowcard.mhra.gov.uk/. Any adverse event should also be reported to Pharmacovigilance at Alliance Pharmaceuticals Limited

Tel: 01249 466 966 or email: [email protected]

You are now leaving the UK healthcare professionals section of the website.

You will be returned to the public section of the website.

Are you a health care professional?

This section of the website has been created to provide UK healthcare professionals with information regarding Gelclair®