Skip to content

The effects of Portulaca Oleracea extract on thirsty and 24 hour urine indices

The effects of Portulaca Oleracea extract on thirsty and 24 hour urine indices in patients with renal stone: a double-blind randomized placebo-controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170725035305N4
Enrollment
60
Registered
2020-05-02
Start date
2020-07-22
Completion date
Unknown
Last updated
2020-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with kidney stones. Calculus of kidney and ureter

Interventions

Intervention 1: Intervention group: The intervention group (n = 30) received a capsul containing of 2 grams Portulaca Oleracea hydro alcoholic extract and half a gram of brown sugar should be taken w

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age 18-65 years Literate

Exclusion criteria

Exclusion criteria: Patients with diabetes Oral problems No use of angiotensin II inhibitors Patients with colds

Design outcomes

Primary

MeasureTime frame
Serum Potassium level. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;Serum Sodium level. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;24-hour urine uric acid. Timepoint: At the start of the study and at the end of the study. Method of measurement: 24 h Urine collection.;24-hour urine citrate. Timepoint: At the start of the study and at the end of the study. Method of measurement: 24 h Urine collection.;Specific weight of urine. Timepoint: At the start of the study and at the end of the study. Method of measurement: Urine sample.;24 hour urine calcium. Timepoint: At the start of the study and at the end of the study. Method of measurement: 24 h Urine collection.;24-hour urine creatinine. Timepoint: At the start of the study and at the end of the study. Method of measurement: 24 h Urine collection.;24-hour urine Na. Timepoint: At the start of the study and at the end of the study. Method of measurement: 24 h Urine collection.

Secondary

MeasureTime frame
Thirst intensity. Timepoint: At the start of the study, at the end of the study. Method of measurement: using Visual Analogue Scale.;Serum triglycerid level. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;Serum cholestrol level. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;Serum HDL level. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;Total antioxidant level. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;ESR. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;CRP. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;Serum Uric acid level. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;Serum Creatinine level. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;Serum Urea level. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;Serum calcium level. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.;Venous blood gas. Timepoint: At the start of the study and at the end of the study. Method of measurement: blood sample.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirhesam Alirezaei

Shahid Beheshti University of Medical Sciences

amirhesam124@gmail.com+212 2083112

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 8, 2026