Metformin Safety and Efficacy in Osteoarthritis.
Launched by MOSTAFA BAHAA · Jan 20, 2024
Trial Information
Current as of June 30, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the safety and effectiveness of a medication called Metformin for treating knee osteoarthritis (OA), a common condition that causes pain and can significantly affect daily activities. The trial is currently recruiting participants aged between 30 and 60 years who have been diagnosed with moderate to severe knee OA, based on X-ray results. This trial aims to find out if Metformin can help manage the symptoms of OA and potentially slow down the progression of the disease.
If you or someone you know is interested in participating, it’s important to note that individuals with certain medical conditions or those who have taken specific treatments recently may not be eligible. Participants can expect to receive the study medication and will be monitored throughout the trial to assess their response to the treatment. This research is crucial because, at present, there are few options available to change the course of osteoarthritis, and finding effective treatments could greatly improve the quality of life for many people.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Primary osteoarthritis Patients recruited were between 30 to 60 years of age.
- • X-ray confirmed Kellgren-Lawrence grade II or III severity primary tibiofemoral OA according to the American College of Rheumatology criteria.
- Exclusion Criteria:
- • Patients with age less than 30 years or more than 60 years Patients Presented with active concomitant gastroduodenal disorders, hepatic and renal impairment within last 30 days prior to receiving the study drug Patients Were diagnosed to have any inflammatory arthritis, gout or acute trauma of the knee, hip or spine; accompanying OA of the hip of sufficient severity to interfere with the functional assessment of the knee Patients had previous or ongoing treatment with oral SYSDOA (e.g., glucosamine sulphate, chondroitin sulphate, diacerein, piascledine), anti-depressants, tranquillisers, antacids or antibiotics; were having active cardiac lesion or hypertension, were pregnant females and those who were planning their pregnancy during the study Patients having a known hypersensitivity to the used medications Patients have persistent diarrhoea or laxative use; severe gastrointestinal disorders, severe obesity, severe parenchymal organ disease, or anaemia (haemoglobin\< 10.0 g/ dl or haematocrit \< 30%).
- • Patients who received oral, intramuscular, intraarticular or soft tissue injections of corticosteroids within last eight weeks before receiving the first dose of the study medication or had undergone joint lavage and arthroscopic procedures in the previous 6 months, were also excluded.
About Mostafa Bahaa
Mostafa Bahaa is a dedicated clinical trial sponsor committed to advancing medical research and patient care through rigorous and ethical clinical studies. With a focus on innovative therapeutic solutions, the organization collaborates with leading researchers and healthcare institutions to ensure the highest standards of scientific integrity and regulatory compliance. Mostafa Bahaa prioritizes patient safety and data transparency, striving to contribute valuable insights that enhance treatment options and improve health outcomes across diverse medical fields.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Damietta, New Damietta, Egypt
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported