Informations générales (source: ClinicalTrials.gov)
Evaluation of the Effect of Hydration About Orthostatic Hypotension in the Elderly. Difference With Venous Compression. A Randomized Controlled Crossover Trial. (CHHO)
Interventional
N/A
Central Hospital, Nancy, France (Voir sur ClinicalTrials)
juillet 2014
juin 2016
29 juin 2024
Primary objective: To compare the decrease in systolic blood pressure between hydration
and venous contention when switching to a standing position. Hypothesis in that hydration
is better than venous contention.
Secondary objective: To evaluate the effect of hydration on lowering systolic blood
pressure during the passage standing in elderly patients with orthostatic hypotension.
Inclusion criteria: Patient aged over 75 years old with orthostatic hypotension proved to
1 and / or 3 min
Etablissements
| Les établissements hors Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| Centre Hospitalier Régional Universitaire de Nancy - 54000 - Nancy - France | Athanase Benetos, Pr | Contact (sur clinicalTrials) | |||
| Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
| Maison Hospitalière Saint Charles - 54000 - Nancy - France | NOEL-RUEF Marie-Hélène | Contact (sur clinicalTrials) | |||
Critères
Tous
Inclusion Criteria:
- Patient aged 75 and older with orthostatic hypotension proved to 1 and / or 3
minutes.
- Written consent of the subject
- Hospitalization or stay expected minimum 3 days
- Affiliation to a social security scheme
- Patient aged 75 and older with orthostatic hypotension proved to 1 and / or 3
minutes.
- Written consent of the subject
- Hospitalization or stay expected minimum 3 days
- Affiliation to a social security scheme
- bedridden patient or without possibility of verticalization
- Patient who can't stand up (pulmonary embolism with high risk)
- Patient who refuse to participate in the study
- Patient with legal protection
- State or condition that may affect the stability of blood pressure during the study
(hyperthermia, modification antihypertensive treatments less than 48 hours before
inclusion...)
- Pathology preventing hydration: Heart failure with less than 1 Liter water
restriction, swallowing disorders preventing hydration orally, inability to
nutrition and hydration orally
- Intravenous or subcutaneous hydration (intravenous or subcutaneous treatments not
included)
- Patient who can't have venous contention: Blue phlebitis, septic thrombosis,
arteritis with score less than 0.6, varicose ulcers during treatment