Health Condition 1: M674- Ganglion
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patient having wrist ganglion (diagnosed clinically and by USG) for the duration of 6 months or less. 2. Age 18 years and above. 3. Gender: Both Male and Female. 4. Willing to give informed consent to participate in the study. 5. Patient must not be under any treatment for wrist ganglion at-least for last one month. (If under previous treatment within last one month, washout period will be allowed for one month from the last date of intake of previous medicine.)
Exclusion criteria
Exclusion criteria: 1. Patients who are immune-compromised and/or suffering from critical illness. 2. Patients who are severely drug/alcohol addicted. 3. Patients unable or unwilling to give informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Outcome name: Changes in size of wrist ganglion Metric/Method of measurement: In mm scale (clinically and by USG)Timepoint: 8 months from the baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Outcome name: Pain Metric/Method of measurement: VAS scoreTimepoint: Every month from the baseline till 8 months;2. Outcome name: Pain and functional difficulties in activities. Metric/Method of measurement: PRWE scoreTimepoint: Every month from the baseline till 8 months | — |
Countries
India
Contacts
Clinical Research Unit for Homoeopathy, Siliguri