The effect of Valerian capsule on the quality of sleep in patients with heart surgery
- Conditions
- The quality of sleep in patients with heart surgery.
- Registration Number
- IRCT2017080124080N11
- Lead Sponsor
- Vice chancellor for research Lorestan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Inclusion criteria :
Non-emergency open-heart surgery?age group 40-80 years old? first heart surgery? routine operation in the operating room? use of foot saphenous vein and left internal mammary artery? Post ICU post-operative second day? Alert? lacking Tracheal tube? Understanding the content in Farsi? lack of history of seizure and psychiatric disorders?lack of drug and alcohol? lack of intra-aortic pump?no sleep disorders known prior to admission? EF more than 30%? Patient's satisfaction to participate in the research? Use of the heart and lung pump ?no history of lung, kidney and liver failure? normal creatinine?no use of herbal medicines Effects on sleeping? not taking hypnotic drugs and antidepressants 3 months before the start of the study? lack of allergy to valerian and other herbal remedies with sedation such as chamomile? lavender and, etc.? lack of pregnancy at the beginning of the study? blood pressure of more than 100 mmHg .
Exit criteria:
The complications of surgery during the study? the need for intra-aortic pump? the reluctance to continue to participate in the research? the lack of drug for one week? allergy to valerian in the study time, pregnancy at the time of study? the existence of individual and family crises such as divorce Or the death of the first degree relatives during the study period?the patient's death? severe insomnia? coagulation disorder during the admission? the occurrence of cognitive impairment.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sleep. Timepoint: Pre-intervention - 3, 14 and 30 days later intervention. Method of measurement: Pittsburgh Sleep Quality Questionnaire.
- Secondary Outcome Measures
Name Time Method