Treatment of secondary lymphedema of the upper limb with cyclo 3 fort
Identifieur interne : 000B97 ( PascalFrancis/Corpus ); précédent : 000B96; suivant : 000B98Treatment of secondary lymphedema of the upper limb with cyclo 3 fort
Auteurs : R. V. Cluzan ; F. Alliot ; S. Ghabboun ; M. PascotSource :
- Lymphology [ 0024-7766 ] ; 1996.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Fifty seven patients with secondary lymphedema of the upper limb after previous treatment for breast cancer were treated for 3 months with an extract of Ruscus + Hesperidin Methyl Chalcone (CYCLO 3 FORT) or placebo according to a double-blind protocol in the context of a controlled clinical trial. All patients also underwent manual lymphatic drainage twice a week for at least one month. With CYCLO 3 FORT, the reduction in volume of arm edema, the main assessment criteria, was 12.9% after 3 months of treatment as compared with a placebo (p=0.009). Decreased edema tended to be more marked in the forearm compared with the upper arm where excess fat deposition seemed to dominate over excess fluid accumulation. CYCLO 3 FORT was well tolerated with minimal adverse reaction.
Notice en format standard (ISO 2709)
Pour connaître la documentation sur le format Inist Standard.
pA |
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Format Inist (serveur)
NO : | PASCAL 96-0216041 INIST |
---|---|
ET : | Treatment of secondary lymphedema of the upper limb with cyclo 3 fort |
AU : | CLUZAN (R. V.); ALLIOT (F.); GHABBOUN (S.); PASCOT (M.) |
AF : | Unité de Lymphologie, Hôpital Cognacq-Jay/Paris/France (1 aut., 2 aut., 3 aut., 4 aut.) |
DT : | Publication en série; Niveau analytique |
SO : | Lymphology; ISSN 0024-7766; Coden LYMPBN; International; Da. 1996; Vol. 29; No. 1; Pp. 29-35; Bibl. 11 ref. |
LA : | Anglais |
EA : | Fifty seven patients with secondary lymphedema of the upper limb after previous treatment for breast cancer were treated for 3 months with an extract of Ruscus + Hesperidin Methyl Chalcone (CYCLO 3 FORT) or placebo according to a double-blind protocol in the context of a controlled clinical trial. All patients also underwent manual lymphatic drainage twice a week for at least one month. With CYCLO 3 FORT, the reduction in volume of arm edema, the main assessment criteria, was 12.9% after 3 months of treatment as compared with a placebo (p=0.009). Decreased edema tended to be more marked in the forearm compared with the upper arm where excess fat deposition seemed to dominate over excess fluid accumulation. CYCLO 3 FORT was well tolerated with minimal adverse reaction. |
CC : | 002B02F08 |
FD : | Lymphoedème; Membre supérieur; Secondaire; Hespéridine; Chimiothérapie; Traitement; Exploration; Homme; Etude comparative; Flavonoïde; Veinotrope |
FG : | Appareil circulatoire pathologie; Lymphatique pathologie |
ED : | Lymphedema; Upper limb; Secondary; Hesperidin; Chemotherapy; Treatment; Exploration; Human; Comparative study; Flavonoid; Venotropic agent |
EG : | Cardiovascular disease; Lymphatic vessel disease |
GD : | Aufbereiten; Vergleich |
SD : | Linfedema; Miembro superior; Secundario; Quimioterapia; Tratamiento; Exploración; Hombre; Estudio comparativo; Flavonoide; Venotrópico agente |
LO : | INIST-14604.354000044471330060 |
ID : | 96-0216041 |
Links to Exploration step
Pascal:96-0216041Le document en format XML
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<front><div type="abstract" xml:lang="en">Fifty seven patients with secondary lymphedema of the upper limb after previous treatment for breast cancer were treated for 3 months with an extract of Ruscus + Hesperidin Methyl Chalcone (CYCLO 3 FORT) or placebo according to a double-blind protocol in the context of a controlled clinical trial. All patients also underwent manual lymphatic drainage twice a week for at least one month. With CYCLO 3 FORT, the reduction in volume of arm edema, the main assessment criteria, was 12.9% after 3 months of treatment as compared with a placebo (p=0.009). Decreased edema tended to be more marked in the forearm compared with the upper arm where excess fat deposition seemed to dominate over excess fluid accumulation. CYCLO 3 FORT was well tolerated with minimal adverse reaction.</div>
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