NCT07709312

Brief Summary

this study aims to measure The Effect of Gingko Biloba on the Clinical Outcome of Rheumatoid Arthritis Patients ,the outcomes are hsCRp,calprotectin,DAS-28,HAQ-DI

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
50

participants targeted

Target at P25-P50 for phase_2

Timeline
2mo left

Started Jul 2026

Shorter than P25 for phase_2

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress19%
Jul 2026Oct 2026

First Submitted

Initial submission to the registry

July 12, 2026

Completed
3 days until next milestone

Study Start

First participant enrolled

July 15, 2026

Completed
1 day until next milestone

First Posted

Study publicly available on registry

July 16, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 15, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 15, 2026

Last Updated

July 16, 2026

Status Verified

July 1, 2026

Enrollment Period

3 months

First QC Date

July 12, 2026

Last Update Submit

July 12, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • HsCRP

    * Blood samples will be drawn from the patients at baseline and after 12 weeks of intervention Blood samples will be collected at baseline ,centrifuged and stored as serum at -80 °C until analysis. * Hs-CRP will be evaluated by for each patient at baseline and after 12 weeks using commercial ELISA kits

    baseline and 12 weeks

Secondary Outcomes (3)

  • calprotectin

    baseline and 12weeks

  • DAS-28

    baseline and 3 months

  • Quality of life assessment

    at baseline and after 12 weeks

Study Arms (2)

ginkgo biloba group

EXPERIMENTAL

Ginkgo biloba group: 25 patients will receive Ginkgo biloba treatment (120 mg twice daily for 12 weeks) in addition to their standard treatment.

Drug: Ginkgo Biloba Extract (120 mg ) manufuctured by EMA PHARM

control group

NO INTERVENTION

Control group: 25 patients will receive standard treatment for 12 weeks.

Interventions

Ginkgo biloba leaf extract (GBLE) has an antioxidant action as a free radical scavenger, an improving effect on blood flow or microcirculation, and a stimulating effect on neurotransmitters. Besides a direct scavenging action on active oxygen species, GBLE exerts an anti-inflammatory effect on inflammatory cells by suppressing the production of active oxygen and nitrogen species. GBLE inhibited the increase in the products of the oxidative decomposition low-density lipoprotein (LDL), reduced the cell death in various types of neuropathies, and prevented the oxidative damage to mitochondria

ginkgo biloba group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may not qualify if:

  • \- 1. Patients with known hypersensitivity to Ginkgo biloba 2. Patients receiving Ginkgo biloba for any other indications 3. Patients on biologic DMARDs 4. Patients with impaired liver functions (liver transaminases level ≥ three times upper normal limits), impaired kidney functions (estimated glomerular filtration rate (eGFR) \< 30 ml/min), 5. Patients with any of the following comorbidities: congestive heart failure, history of myocardial infarction, severe anemia, active infections, other inflammatory diseases, and malignancies.
  • \. Patients with other autoimmune diseases

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Arthritis, Rheumatoid

Interventions

Ginkgo biloba extract

Condition Hierarchy (Ancestors)

ArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic DiseasesConnective Tissue DiseasesSkin and Connective Tissue DiseasesAutoimmune DiseasesImmune System Diseases

Central Study Contacts

noran sameh ahmed, bachelor degree in pharmacy

CONTACT

Study Design

Study Type
interventional
Phase
phase 2
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
noran sameh ahmed

Study Record Dates

First Submitted

July 12, 2026

First Posted

July 16, 2026

Study Start

July 15, 2026

Primary Completion (Estimated)

October 15, 2026

Study Completion (Estimated)

October 15, 2026

Last Updated

July 16, 2026

Record last verified: 2026-07