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Effectiveness of propolis in reducing the symptoms of rheumatic diseases in humans

Propolis effectiveness of therapy in the treatment of signs and symptoms of rheumatism: Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7g8p6s
Enrollment
Unknown
Registered
2016-10-19
Start date
2015-04-20
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Rheumatic Diseases

Interventions

One hundred and twenty adults (aged 18-70) living in the State of Alagoas, Brazil, with rheumatic pains were recruited from the waiting list in public clinics in the state of Alagoas. After an initial
Other
D27.505.954.329
V03.175.250

Sponsors

Pós Graduação em Ciências da Saúde
Lead Sponsor
Pós Graduação em Ciências da Saúde
Collaborator
Universidade de Ciências da Saúde de Alagoas
Collaborator

Eligibility

Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were the clinical diagnosis of tendinitis; bursitis or osteoarthritis and presence of pain resulting from rheumatic disease at the time of initial evaluation. Participants did not do any treatment for rheumatism two weeks before the start or during the clinical trial; or intra-articular corticosteroid injections in the previous three months.

Exclusion criteria

Exclusion criteria: We excluded patients with hypersensitivity to bee toxins, obesity, pregnancy and lactation, gastrointestinal bleeding history, gastric perforation; kidney disease, liver disease; current history of alcoholism, use of anticoagulants; implant prosthesis or pacemaker; severe chronic uncontrolled (hypertension, diabetes mellitus, heart disease and other diseases that by its nature or the proposed treatment could interfere with the assessment).

Design outcomes

Primary

MeasureTime frame
Pain intensity decreased to articulate said recorded by visual numeric pain scale from obtaining reduction of 3 or more degrees of pain on said scale pre and post intervention.;Increased angulation range of motion (ROM) joint, checked with the goniometry technique, from the observation of an increase of over 30 degrees of ROM, pre and post intervention.;Improvement in muscle strength tested by manual muscle strength testing, with power increased in a statistically significant way, pre and post intervention.

Secondary

MeasureTime frame
No reported side effects, checked complaint from the researcher. It was reported no effect throughout the research.

Countries

Brazil

Contacts

Public ContactCamila Sales

Pós Graduação em Ciências da Saúde

camila.mourasales@gmail.com+55(82)999297656

Outcome results

None listed

Source: REBEC (via WHO ICTRP)