Efficacy and Tolerability of Amitriptylinoxide in the Treatment of Chronic Tension-Type Headache: A Multi-Centre Controlled Study

Author:

Pfaffenrath V1,Diener H-C2,Isler H3,Meyer C4,Scholz E5,Taneri Z6,Wessely P7,Zaiser-Kaschel H8,Haase W9,Fischer W10

Affiliation:

1. Neurological Practice1, Munich, Germany

2. Department of Neurology2, University of Essen, Essen, Germany

3. Department of Neurology3, University of Zürich, Zürich, Switzerland

4. Neurological Practice4, Baden, Switzerland

5. Neurological Practice5, Böblingen, Germany

6. Neurological Practice6, Duisburg, Germany

7. Department of Neurology7, University of Wien, With, Austria

8. Psychological Practice8, Köngen, Germany

9. Institut für numerische Statistik9, Köln, Germany

10. Clinical Research10, Bonn, Germany

Abstract

Amitriptyline is the medication of first choice in the treatment of chronic tension-type headache. In 197 patients with chronic tension-type headache (87M and 110F with a mean age of 38 ±13 (18–68)) efficacy and tolerability of 60–90 mg amitriptylinoxide (AO) were compared with 50–75 mg amitriptyline (AM) and placebo (PL) in a double-blind, parallel-group trial consisting of a four weeks' baseline phase and 12 weeks of treatment. The primary study endpoint was a reduction of at least 50% of the product of headache duration and frequency and a reduction of at least 50% in headache intensity. Statistics used were Fisher's exact test and analysis of variance. No significant difference emerged between AO, AM and PL with respect to the primary study endpoint. Treatment response occurred in 30.3% of the AO, 22.4% of the AM and 21.9% of the PL group. A reduction in headache duration and frequency of at least 50% was found in 39.4% on AO, in 25.4% on AM and in 26.6% on PL (PAO-PL = .1384, PAM-PL = 1.000, PAO-AM = .0973). A reduction in headache intensity of at least 50% was found in 31.8% on AO, in 26.9% on AM and in 26.6% on PL (PAO-PL = .5657, PAM-PL = 1.000, PAO-AM = .5715). Trend analysis with respect to a significant reduction of headache intensity ( p < 0.05) and the product of headache duration and frequency revealed a superior effect of AO. Adverse events occurred in 75.8% on AO, 82.1% on AM and 76.6% on PL (PAO-PL = 1.000, PAM-PL =.5188, PAO-AM = .4017). Neither depressive symptoms, measured by the SCL-90-R, nor study drug-related adverse events had any influence on the results.

Publisher

SAGE Publications

Subject

Clinical Neurology,General Medicine

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