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effect of Melissa officinalis in treatment of patient with Rheumatoid arthritis

Pilot evaluation of the anti-inflamation and analgesics effect of oral administration of Melissa officinalis in patients with Rheumatoid arthritis: a double-blind randomized crossover trial

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201126049498N1
Enrollment
20
Registered
2021-03-10
Start date
2021-03-06
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Rheumatoid arthritis disease. Rheumatoid arthritis, unspecified

Interventions

Intervention 1: Melissa officinalis is a perennial herbaceous plant in the mint family (Lamiaceae). Scientific research of this plant shows that it has anti-inflammatory, analgesic, and anti-depressa

Sponsors

Shahed University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patient satisfaction and signing of informed consent form Diagnosis of patients with moderate Rheumatoid Arthritis Using the Criteria of the American College of Rheumatology Patients over 18 years During the period of the disease up to 15 years DAS Score between 3-5

Exclusion criteria

Exclusion criteria: Lack of cooperation of patients History of Heart, kidney, liver and ... diseases Pregnancy Any kind of Immunodeficiency diseases No other autoimmune diseases

Design outcomes

Primary

MeasureTime frame
Evaluation of Disease Activity Score 28 (DAS 28). Timepoint: 2 months after and before treatment. Method of measurement: DAS Calculator software.;Evaluation of ESR (Erythrocyte Sedimentation Rate. Timepoint: 2 months after and before treatment. Method of measurement: Using Westergren method.;Evaluation of Rheumatoid Factor (RF). Timepoint: 2 months after and before treatment. Method of measurement: Quantitative method with diagnostic kit.;Evaluation of CRP (C-Reactive Protein). Timepoint: 2 months after and before treatment. Method of measurement: Quantitative method with diagnostic kit.;Evaluation of Anti ccp (Cyclic Citrirullinated Peptide). Timepoint: Before treatment. Method of measurement: ELISA method.;Assay of TNF-a (Tumor necrosis factor a). Timepoint: 2 months after and before treatment. Method of measurement: ELISA method.;Assay of Interleukin 17 (IL-17). Timepoint: 2 months after and before treatment. Method of measurement: ELISA method.;?Evaluation of visual analog scale (VAS). Timepoint: 2 months after and before treatment. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Evaluation of World Health Organization Quality of Life-BREF (WHOQOL-BREF). Timepoint: 2 months after and before treatment. Method of measurement: Questionnaire.;Evaluation of Beck Depression Inventory (BDI-II). Timepoint: 2 months after and before treatment. Method of measurement: Questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzadeh Mizani

Shahed University

azadeh.mizani@yahoo.com+98 21 6641 8331

Outcome results

None listed

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