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theraputic effects of celery, dill and green tea combination in treatment of metabolic syndrome in patients with schizophrenia

Comparing theraputic effects of celery, dill and green tea combination with placebo in treatment of metabolic syndrome in patients with schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013102915206N1
Enrollment
60
Registered
2014-02-24
Start date
2013-06-26
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Schizophrenia. Schizophrenia

Interventions

Intervention 1: Intervention group: prescription of tablet composed of extracts of celery, dill, and green tea three times a day half an hour before meal for 3 consecutive months. Intervention 2: Cont
Treatment - Drugs
Placebo
Intervention group: prescription of tablet composed of extracts of celery, dill, and green tea three times a day half an hour before meal for 3 consecutive months.
Control group: prescription of a tablet with identical appearance to the herbal combination tablet three times a day half an hour before meal for 3 consecutive months.

Sponsors

University of social welfare and rehabilitation sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: diagnosis of schizophrenia and metabolic syndrome; age between 18 and 65 years; female; agreement of patient and her guardian towards participation in the trial. Exclusion criteria: any change in the schizophrenia medication within two months prior to the trial; coexistence of another major mental disorder; any hyper sensitive reaction to the medication; exacerbation of mental symptoms.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Weist circumference. Timepoint: 3 months. Method of measurement: By a regular meter,cm.;Blood pressure. Timepoint: 3 months. Method of measurement: Pressure guage,mmHg.;Fasting blood sugar. Timepoint: 3 months. Method of measurement: md/ml, evaluation of venous blood sample by spectrophotometer.;HDL(high density lipoprotein). Timepoint: 3 months. Method of measurement: mg/ml, evaluation of venous blood sample by spectrophotometer.;TG(triglycerides). Timepoint: 3 months. Method of measurement: mg/ml, evaluation of venous blood sample by spectrophotometer.

Secondary

MeasureTime frame
Gastrointestinal dyscomfort. Timepoint: 3 months after intervention. Method of measurement: Personal interview.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactEmytis Tavakoli

University of social welfare and rehabilitation sciences

tavakoli79@yahoo.com; em.tavakoli@uswr.ac.ir+98 21 3340 1604

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026