Trigger Finger. Trigger finger, unspecified finger
Conditions
Interventions
Intervention 1: Intervention group:Medicines from Abaidi Company are selected for all patients equally. Hemoglobin A1C is measured before treatment was started. 20 mg methylprednisolone acetate inject
Sponsors
Babol University of Medical Sciences
Eligibility
Sex/Gender
All
Age
21 Years to 65 Years
Inclusion criteria
Inclusion criteria: Age 65-95 years Patients with Trigger Finger Informed consent of patient in the study
Exclusion criteria
Exclusion criteria: Patients who had a history of allergy to Diclofenac or Methylprednisolone. Pregnant or lactating patients and patients who have had a previous history of injection on the same finger. Failure to follow the patient
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Decrease in Quinnell grade. Timepoint: 3 and 6 weeks, 3 and 6 and 12 months after the first injection. Method of measurement: Quinnell grading. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Sasan Mohammadi Jami
Babol University of Medical Sciences
Outcome results
None listed