Aspartame study: Determination of the symptoms of aspartame in subjects who have reported symptoms in the past compared to controls

Completed

• Conditions: Safety study to assess the effect of aspartame; Nutritional, Metabolic, Endocrine

• Registration Number: ISRCTN39650237
• Lead Sponsor: Hull and East Yorkshire Hospitals NHS Trust (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2012-10-11
• Last Update Posted: 17 October 2016

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 150

Inclusion Criteria

Healthy volunteers:
1. No known allergies
2. No concomitant medical condition
3. No medication

Aspartame reactors:
1. Reported effect of aspartame on ingestion
2. No allergies to other food substances

Exclusion Criteria

1. Allergies to food or medication
2. A concomitant medical condition
3. Prescription medication
4. Refusal for GP to be informed

Aspartame reactors:
1. Allergies to food or medication
2. A concomitant medical condition
3. Prescription medication
4. Refusal for GP to be informed

Study & Design

• Study Type: Interventional
• Study Design: Not specified