quality of life.
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age 18 years and above Dialysis adequacy index above 1/2 At least 3 months have passed since the start of hemodialysis Having at least two of the criteria of Rome-3
Exclusion criteria
Exclusion criteria: Sensitivity to plant compounds, especially Cassia fistula History of active infection in the last month Absence of gastrointestinal diseases including irritable bowel syndrome, secondary constipation or neurological diseases (Parkinson's, depression, etc.) Non-neurological diseases (hypothyroidism, hypokalemia, etc.) History of any gastrointestinal surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of Life Score in the Patient Assessment of Constipation Quality of Life (PAC-QOL) questionnaire. Timepoint: Measurement of quality of life before the intervention and 30 days after the start of Cassia fistula syrup. Method of measurement: Patient Assessment of Constipation Quality of Life (PAC-QOL) questionnaire.;Constipation score in the Constipation Assessment Scale (CAS). Timepoint: Measurement of Constipation before the intervention and 30 days after the start of Cassia fistula syrup. Method of measurement: Constipation Assessment Scale (CAS).;Frequency and frequency of defecation. Timepoint: Measurement of the frequency of defecation on a daily basis the start of Cassia fistula syrup. Method of measurement: Make a note in the checklist.;Stool consistency in the Bristol stool scale. Timepoint: Measurement of the stool consistency after each bowel movement after starting Cassia fistula syrup. Method of measurement: Bristol stool scale.;Digestive problems. Timepoint: Measurement of the Digestive problems after each bowel movement after starting Cassia fistula syrup. Method of measurement: Make a note in the checklist.;Measurement of blood sodium. Timepoint: Measurement of blood sodium before intervention, two weeks after and four weeks after intervention. Method of measurement: blood test.;Measurement of blood potassium. Timepoint: Measurement of blood potassium level before the intervention, two weeks after and four weeks after the intervention. Method of measurement: blood test.;Measurement of blood hemoglobin. Timepoint: Measurement of blood hemoglobin level before the intervention and four weeks after the intervention. Method of measurement: blood test.;Measurement of blood hematocrit. Timepoint: Measurement of blood hematocrit before intervention and four weeks after intervention. Method of measurement: blood test.;Blood platelet count. Timepoint: Measurement of blood platelet count before the intervention and four weeks after the intervention. Met | — |
Secondary
| Measure | Time frame |
|---|---|
| Itching score in the Itchy Quality of Life (ItchyQoL) questionnaire. Timepoint: Measurement of pruritus before the intervention and 30 days after the start of Cassia fistula syrup. Method of measurement: Itchy Quality of Life (ItchyQoL) questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Shahed University