Hyaloglide® is a hyaluronan-based gel based on a novel auto-crosslinked technology designed to reduce postsurgical adhesions. Its efficacy was assessed in a multicentred randomized controlled trial comparing the results of flexor tenolysis in zone 2 following failed flexor tendon repairs. In the control group a standard release was performed. In the treated group, Hyaloglide® was applied into the flexor sheath and around the site of tenolysis. Forty-five patients, 19 controls and 26 treated with Hyaloglide®, were enrolled in 13 centres. All the patients were evaluated at 30, 60, 90 and 180 days after surgery by testing Total Active Motion, Quick-DASH questionnaire and number of working days lost after surgery. Patients in the Hyaloglide® group had a statistically better recovery of finger motion at all time intervals and returned earlier to work and daily activities. The use of Hyaloglide® did not appear to increase the complication rate. © 2010 The British Society for Surgery of the Hand.
Efficiency of hyaloglide ® in the prevention of the recurrence of adhesions after tenolysis of flexor tendons in zone II: A randomized, controlled, multicentre clinical trial / Riccio, M., Battiston, B., Pajardi, G., Corradi, M., Passaretti, U., Atzei, A., Altissimi, M., Vaienti, L., Catalano, F., Del Bene, M., Fasolo, P., Ceruso, M., Luchetti, R., Landi, A., Bertani, A., Campodonico, A., Pangrazi, P.P., Marchesini, A., Leti Acciaro, A., Castagnetti, G.C., et al.. - In: JOURNAL OF HAND SURGERY. EUROPEAN VOLUME. - ISSN 1753-1934. - 35:2(2010), pp. 130-138. [10.1177/1753193409342044]
Efficiency of hyaloglide ® in the prevention of the recurrence of adhesions after tenolysis of flexor tendons in zone II: A randomized, controlled, multicentre clinical trial
Leti Acciaro A.
;Rocchi L.
2010
Abstract
Hyaloglide® is a hyaluronan-based gel based on a novel auto-crosslinked technology designed to reduce postsurgical adhesions. Its efficacy was assessed in a multicentred randomized controlled trial comparing the results of flexor tenolysis in zone 2 following failed flexor tendon repairs. In the control group a standard release was performed. In the treated group, Hyaloglide® was applied into the flexor sheath and around the site of tenolysis. Forty-five patients, 19 controls and 26 treated with Hyaloglide®, were enrolled in 13 centres. All the patients were evaluated at 30, 60, 90 and 180 days after surgery by testing Total Active Motion, Quick-DASH questionnaire and number of working days lost after surgery. Patients in the Hyaloglide® group had a statistically better recovery of finger motion at all time intervals and returned earlier to work and daily activities. The use of Hyaloglide® did not appear to increase the complication rate. © 2010 The British Society for Surgery of the Hand.| File | Dimensione | Formato | |
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