Efficacy, Safety, and Tolerability of Ultra-high-caloric, Fatty Diet (UFD) in Amyotrophic Lateral Sclerosis (ALS)

Status: Recruiting
Location: See all (23) locations...
Intervention Type: Other, Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims at evaluating efficacy and tolerability of an ultra-high-caloric, fatty diet (UFD) compared to placebo in patients with amyotrophic lateral sclerosis (ALS).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Possible, probable (clinically or laboratory supported) or definite amyotrophic lateral sclerosis according to the revised version of the El Escorial criteria

• Disease duration (onset of first paresis or bulbar symptoms) \< 24 months

• Loss of amyotrophic lateral sclerosis functional rating scale revised of ≥ 0.33 points/month based on the formula: (48 - myotrophic lateral sclerosis functional rating scale revised score at screening visit) / (months between onset and screening visit)

• Age ≥18 years.

• Either continuously treated with a stable dose of riluzole, OR not treated with riluzole for the last 4 weeks prior to inclusion

• Either continuously treated with a stable dose of edaravone, OR not treated with edaravone for the last 4 weeks prior to inclusion

• Either continuously treated with a stable dose of sodium-phenylbutyrate/taurursodiol, OR not treated with sodium-phenylbutyrate/taurursodiol for the last 4 weeks prior to inclusion

• Capable of thoroughly understanding all information given

• full written informed consent according to good clinical practice

Locations
Other Locations
Germany
RWTH Aachen
NOT_YET_RECRUITING
Aachen
Charité Universitätsmedizin Berlin
RECRUITING
Berlin
University Clinic Bochum
NOT_YET_RECRUITING
Bochum
University Clinic Bonn
NOT_YET_RECRUITING
Bonn
Technical University Dresden
NOT_YET_RECRUITING
Dresden
University Clinic Erlangen
NOT_YET_RECRUITING
Erlangen
Alfried Krupp Krankenhaus Essen
NOT_YET_RECRUITING
Essen
University Clinic Göttingen
NOT_YET_RECRUITING
Göttingen
University Clinic Halle
NOT_YET_RECRUITING
Halle
Hannover Medical School
NOT_YET_RECRUITING
Hanover
University Clinic Jena
NOT_YET_RECRUITING
Jena
DRK Clinic Kassel
NOT_YET_RECRUITING
Kassel
Klinikum Kempten
NOT_YET_RECRUITING
Kempten
University Clinic Leipzig
NOT_YET_RECRUITING
Leipzig
University Clinic Lübeck
RECRUITING
Lübeck
Diakonissenkrankenhaus Mannheim
RECRUITING
Mannheim
Technical University Munich
NOT_YET_RECRUITING
Munich
University Clinic Münster
NOT_YET_RECRUITING
Münster
University Clinic Regensburg
NOT_YET_RECRUITING
Regensburg
University Clinic Rostock
NOT_YET_RECRUITING
Rostock
University of Ulm
RECRUITING
Ulm
DKD HELIOS Clinic Wiesbaden
RECRUITING
Wiesbaden
University Clinic Würzburg
NOT_YET_RECRUITING
Würzburg
Contact Information
Primary
Johannes Dorst, Prof. Dr.
johannes.dorst@uni-ulm.de
+497311775285
Time Frame
Start Date: 2024-06-01
Estimated Completion Date: 2027-06-01
Participants
Target number of participants: 392
Treatments
Experimental: Ultra-high-caloric fatty diet
ultra-high-caloric, high-fat, fluid nutritional supplement oral intake of 4 times 35 ml per day in addition to normal food intake, corresponding to +630 kcal and +70g fat per day
Placebo_comparator: Placebo
placebo, fluid nutritional supplement oral intake of 4 times 35 ml per day in addition to normal food intake, corresponding to +50 kcal and +3,5g fat per day
Sponsors
Leads: University of Ulm

This content was sourced from clinicaltrials.gov

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