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Comparative efficacy and safety of triple therapy (ramipril, telmisartan, hydrochlorothiazide) vs dual anti hypertensive therapy (ramipril or telmisartan, hydrochlorothiazide) in stage 2 hypertensive patients.
Bhushan, Bharat; Gupta, Seema; Khajuria, Vijay; Kumar, Dinesh; Lal, Mohan; Kumar, Dharminder; Bhat, Sanjeev; Sharma, Aman.
Afiliación
  • Bhushan B; Resident, Department of Pharmacology, Government Medical College , Jammu, India .
  • Gupta S; Assistant Professor, Department of Pharmacology, Government Medical College , Jammu, India .
  • Khajuria V; Associate Professor, Department of Pharmacology, Government Medical College , Jammu, India .
  • Kumar D; Associate Professor, Department of Preventive and Social Medicine, Government Medical College , Jammu, India .
  • Lal M; Professor, Department of Cardiology, Government Medical College , Jammu, India .
  • Kumar D; Assistant Professor, Department of Cardiology, Government Medical College , Jammu, India .
  • Bhat S; Lecturer, Department of Cardiology, Government Medical College , Jammu, India .
  • Sharma A; Resident, Department of Pharmacology, Government Medical College , Jammu, India .
J Clin Diagn Res ; 8(8): HC25-8, 2014 Aug.
Article en En | MEDLINE | ID: mdl-25302216
ABSTRACT

AIM:

To evaluate the comparative efficacy and safety of ramipril 5mg plus hydrochlorothiazide 12.5mg (R + HCTZ), telmisartan 40mg plus hydrochlorothiazide12.5mg (T + HCTZ) and ramipril 2.5mg plus telmisartan 20mg plus hydrochlorothiazide12.5mg (R + T + HCTZ) in patients with stage 2 hypertension. MATERIALS AND

METHODS:

A prospective, open label, randomized comparative study was conducted to study the comparative efficacy and safety of R+HCTZ (group 1), T+HCTZ (group 2)and R+T+TCTZ (group3) in 88 patients with stage 2 hypertension without co-morbid conditions. Echocardiography was done to assess left ventricular function. Patients were followed up to 24 weeks and any ADR occurring in this period was recorded.

RESULTS:

All the three treatment groups showed significant fall in both systolic and diastolic blood pressure compared to the baseline scores (p<0.0001). Intergroup comparison did not reveal any significant difference. Total number of adverse drug events reported were 15. Group III had higher percentage ADRs. Dry cough (8) was most common ADR. The echocardiography parameters did not change from baseline values with all three treatment regimens.

CONCLUSION:

All three medications were of equal efficacy in patients with stage 2 hypertension without co morbid conditions, failing to prove superiority over each other.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: J Clin Diagn Res Año: 2014 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Clinical_trials Idioma: En Revista: J Clin Diagn Res Año: 2014 Tipo del documento: Article País de afiliación: India