A double-blind, cross-over trial of O-(β-hydroxyethyl)-rutosides (benzo-pyrones) in the treatment of lymphoedema of the arms and legs
Identifieur interne : 00E480 ( Main/Exploration ); précédent : 00E479; suivant : 00E481A double-blind, cross-over trial of O-(β-hydroxyethyl)-rutosides (benzo-pyrones) in the treatment of lymphoedema of the arms and legs
Auteurs : N. B. Piller [Australie] ; R. Gwyn Morgan [Australie] ; J. R. Casley-Smith [Australie]Source :
- British Journal of Plastic Surgery [ 0007-1226 ] ; 1988.
Descripteurs français
- KwdFr :
- Adulte d'âge moyen, Attribution aléatoire, Bras, Complications postopératoires (traitement médicamenteux), Essais cliniques comme sujet, Femelle, Humains, Jambe, Lymphoedème (physiopathologie), Lymphoedème (traitement médicamenteux), Mastectomie, Mâle, Méthode en double aveugle, O-(bêta-Hydroxyéthyl)rutosides (administration et posologie), O-(bêta-Hydroxyéthyl)rutosides (analogues et dérivés), O-(bêta-Hydroxyéthyl)rutosides (usage thérapeutique), Rutoside (analogues et dérivés), Température cutanée ().
- MESH :
- administration et posologie : O-(bêta-Hydroxyéthyl)rutosides.
- analogues et dérivés : O-(bêta-Hydroxyéthyl)rutosides, Rutoside.
- physiopathologie : Lymphoedème.
- traitement médicamenteux : Complications postopératoires, Lymphoedème.
- usage thérapeutique : O-(bêta-Hydroxyéthyl)rutosides.
- Adulte d'âge moyen, Attribution aléatoire, Bras, Essais cliniques comme sujet, Femelle, Humains, Jambe, Mastectomie, Mâle, Méthode en double aveugle, Température cutanée.
English descriptors
- KwdEn :
- Arm, Clinical Trials as Topic, Double-Blind Method, Female, Humans, Hydroxyethylrutoside (administration & dosage), Hydroxyethylrutoside (analogs & derivatives), Hydroxyethylrutoside (therapeutic use), Leg, Lymphedema (drug therapy), Lymphedema (physiopathology), Male, Mastectomy, Middle Aged, Postoperative Complications (drug therapy), Random Allocation, Rutin (analogs & derivatives), Skin Temperature (drug effects).
- MESH :
- chemical , administration & dosage : Hydroxyethylrutoside.
- chemical , analogs & derivatives : Hydroxyethylrutoside, Rutin.
- chemical , therapeutic use : Hydroxyethylrutoside.
- drug effects : Skin Temperature.
- drug therapy : Lymphedema, Postoperative Complications.
- physiopathology : Lymphedema.
- Arm, Clinical Trials as Topic, Double-Blind Method, Female, Humans, Leg, Male, Mastectomy, Middle Aged, Random Allocation.
Abstract
Abstract: A randomised, double-blind, cross-over trial was performed on 26 patients with post-mastectomy lymphoedema of the arm, and 14 with lymphoedema of the leg. For 6 months, patients took O-(β-hydroxyethyl)-rutosides (oxerutin; “Paroven®”, “Venoruton®”, Zyma) in doses of 3 g/day, or the placebos; then they took the reverse. Measurements (volume, circumferences, tonometry and skin temperature) were made monthly. The active drug reduced the volumes of the limbs (p<0.05 to 0.01) and their circumferences (p<0.05 to 0.001). It increased the softness of the limbs, as shown by the increases in the tonometry values (p<0.01 to 0.001). There was a lowering of the elevated skin temperatures (p<0.05 to 0.001). Patients reported increased comfort and freedom of movement, a lessening of their bursting pains, heaviness and tension (p<0.05 to 0.01), and an increased mobility of their limbs (p<0.0001). Most patients (70%) preferred the active drug (p<0.0001). An increase in general well-being was reported by 97% of patients when taking the active drug compared with 4% for the placebo (p<0.0001).
Url:
DOI: 10.1016/0007-1226(88)90139-7
Affiliations:
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Le document en format XML
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<front><div type="abstract" xml:lang="en">Abstract: A randomised, double-blind, cross-over trial was performed on 26 patients with post-mastectomy lymphoedema of the arm, and 14 with lymphoedema of the leg. For 6 months, patients took O-(β-hydroxyethyl)-rutosides (oxerutin; “Paroven®”, “Venoruton®”, Zyma) in doses of 3 g/day, or the placebos; then they took the reverse. Measurements (volume, circumferences, tonometry and skin temperature) were made monthly. The active drug reduced the volumes of the limbs (p<0.05 to 0.01) and their circumferences (p<0.05 to 0.001). It increased the softness of the limbs, as shown by the increases in the tonometry values (p<0.01 to 0.001). There was a lowering of the elevated skin temperatures (p<0.05 to 0.001). Patients reported increased comfort and freedom of movement, a lessening of their bursting pains, heaviness and tension (p<0.05 to 0.01), and an increased mobility of their limbs (p<0.0001). Most patients (70%) preferred the active drug (p<0.0001). An increase in general well-being was reported by 97% of patients when taking the active drug compared with 4% for the placebo (p<0.0001).</div>
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