MILDRONĀTA PIELIETOŠANAS EFEKTIVITĀTE UN DROŠĪBA SLIMNIEKIEM AR MIJKLIBOŠANU (CLAUDICATIO INTERMITTENS)

Authors
Category Primary study
Registry of TrialsEU Clinical Trials Register
Year 2005
INTERVENTION: Trade Name: MILDRONATS Product Name: MILDRONATS Pharmaceutical Form: Capsule* INN or Proposed INN: 3‐(2,2,2‐TRIMETILHIDRAZINIJA)PROPIONATA DIHIDRATS Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 500‐ Pharmaceutical form of the placebo: Capsule* Route of administration of the placebo: Oral use CONDITION: PERIFERO ARTERIJU SLIMIBA (PAS) AR MIJKLIBOŠANU (CLAUDICATIO INTERMITTENS) (II STADIJA PEC FONTAINE) PRIMARY OUTCOME: Main Objective: PETIJUMA MERKIS IR IZVERTET MILDRONATA EFEKTIVITATI UN LIETOŠANAS DROŠIBU KOMBINACIJA AR PAS PAMATTERAPIJU ATTIECIBA UZ PACIENTU AR MIJKLIBOŠANU FIZISKAS SLODZES TOLERANCI, KA NOVERTEŠANAS TESTUS LIETOJOT TREDMILA FIZISKAS SLODZES RAKSTURLIELUMUS Primary end point(s): ABSOLUTAS MIJKLIBOŠANAS DISTANCES (ACD) IZMAINAS, SALIDZINOT ACD PIRMS UN PEC 24 NEDELU ARSTEŠANAS AR MILDRONATU. Secondary Objective: IZVERTET MILDRONATA IETEKMI UZ PACIENTU AR MIJKLIBOŠANU PERIFERO ASINSVADU STAVOKLI (POTITES BRAHIALAIS INDEKSS), PACIENTU VISPAREJO VESELIBAS STAVOKLI (CGIS, CGIC) UN PACIENTU DZIVES KVALITATI INCLUSION CRITERIA: VIRIEŠI UN SIEVIETES NO 40 LIDZ 75 GADU VECUMAM. SIEVIETES NAV GRUTNIECIBAS STAVOKLI VAI BAROJOŠAS AR KRUTI. PACIENTI AR MIJKLIBOŠANU VISMAZ PEDEJOS 6 MENEŠUS AR STABILIEM SIMPTOMIEM VISMAZ 3 MENEŠUS PIRMS PETIJUMA SAKUMA. MIJKLIBOŠANA KA FIZIKAS SLODZES PARTRAUKŠANAS IEMESLS. POTITES‐BRAHIALAIS ARTERIALA SISTOLISKA SPIEDIENA INDEKSS (PBI) = 0,89. PACIENTS SANEM ORDINETO PAMATTERAPIJU. Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18‐64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range
Epistemonikos ID: 40b72ab9d98526067547ad5c3c735c834e79b438
First added on: Aug 21, 2024