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Evaluation of complementary therapy with Capparis spinosa on MS patients

Formulation and clinical evaluation of complementary therapy with Capparis spinosa on MS patients

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180103038199N15
Enrollment
80
Registered
2023-04-13
Start date
2023-04-21
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Multiple sclerosis. Multiple sclerosis

Interventions

Intervention 1: Intervention group: Patients with MS receiving 2 capsules containing 300 mg of Capparis spinosa extract once a day for 3 months. Intervention 2: Control group: Patients with MS receivi

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with multiple sclerosis (MS) Having an EDSS score between zero and 5.5 Having stable and regular drug treatment in the last 4 weeks Consent not to use complementary medicines from 7 days before the start of the intervention until the end of the intervention Age between 18 and 60 years Consent to admission to the study

Exclusion criteria

Exclusion criteria: History of alcohol or drug addiction History of pregnancy or breastfeeding in the last 12 months Kidney and liver dysfunction Treatment with steroids during the last 2 months before the start of the study Having a neurological disease in addition to MS Having cardiovascular or infectious disease Having a history of severe respiratory or skin sensitivity

Design outcomes

Primary

MeasureTime frame
Change in disease symptoms based on EDSS. Timepoint: At the beginning of the study and after 3 months of treatment. Method of measurement: Checklist.

Secondary

MeasureTime frame
Changes in Interleukin-4 levels. Timepoint: At the beginning of the study and after 3 months of treatment. Method of measurement: Laboratory kit.;Changes in Interferon-gamma levels. Timepoint: At the beginning of the study and after 3 months of treatment. Method of measurement: Laboratory kit.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVahid Reza Askari

Mashhad University of Medical Sciences

askariv@mums.ac.ir+98 51 3800 2264

Outcome results

None listed

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