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Dextrose effect in the treatment of pain in osteoarthritis of the knee

Comparison of periarticular & intrarticular Dextrose prolotherapy for pain relief in knee O.A.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015102713364N3
Enrollment
104
Registered
2016-11-02
Start date
2015-04-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Gonarthrosis [arthrosis of knee]. Primary gonarthrosis, bilateral

Interventions

Intervention 1: In group I, 8 ml of Dextrose 10% + lidocaine 1% were injected (inside the knee joint) through a infra patellar approach by a 23 G needle. Injection was repeated at 1 and 2 weeks after
Treatment - Other
In group I, 8 ml of Dextrose 10% + lidocaine 1% were injected (inside the knee joint) through a infra patellar approach by a 23 G needle. Injection was repeated at 1 and 2 weeks after first injection.
In group II, 10 ml of Dextrose 10% + lidocaine 1% was injected subcutaneously at 4 points of periarticular area around the knee.The injection was performed fan wise by 2.5 ml of drug at each point wit

Sponsors

Vice Chancellor for Research and Technology of Shahid Beheshti University Of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with chronic osteoarthritis;age over 50 years;grade 2 or higher of OA in radiology;morning stiffness less than 30 minutes;3 month unresponsiveness to conservative therapy. Exclusion criteria:severe underlying disease;coagulopathy;history of rheumatologic disorders;diabetes; history of corticosteroid therapy in past year;history of prolotherapy in past year;history of intraarticular injection in past year;indication for surgical arthroplasty.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Each month for 3 months. Method of measurement: VAS.;WOMAC Index. Timepoint: Each month for 3 months. Method of measurement: The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC).

Secondary

MeasureTime frame
Patient satisfaction. Timepoint: Each month for 3 months. Method of measurement: 0 = absolutely no pain, 1 = sometimes moderate pain, 2 = moderate pain ever 3 = Only sometimes severe pain, 4 = always moderate pain and sometimes severe pain 5 = Always sharp pain.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrdad Taheri

Shahid Beheshti University of Medical Sciences

taheri.1352@yahoo.com+98 21 7756 7840

Outcome results

None listed

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