Health Condition 1: M659- Synovitis and tenosynovitis, unspecified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients diagnosed with wrist ganglion (ICD-11 Code FB42.2) clinically and by USG. 2. Age 18- 65 years 3. Participants of either sex or transgender 4. Participants having prior experience or knowledge of the treatment. e.g. primed to expect homoeopathic aggravation and available treatment options for the disease conditions, intimated through Patient Information Sheet
Exclusion criteria
Exclusion criteria: 1. Not providing written informed consent of participation. 2. Non-ambulant patients. 3. Patient suffering from active or chronic, systemic or local infection or disease. 4. Patients who are too sick for consultation. 5. Unwilling to take part and not giving consent to join the study 6. Diagnosed cases of unstable mental or psychiatric illness or other uncontrolled or life-threatening illness affecting quality of life. 7. Pregnancy, puerperal women and lactating mother. 8. Tobacco chewing and/or smoking, alcoholism and/or any form(s) of substance abuse and/or dependence (TAPS tool) [21]. 9. Self-reported immune-compromised state, AIDS, hepatitis etc. 10. Undergoing homoeopathic treatment for any chronic disease within last 6 months. 11. Simultaneous participation in any other clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The size (diameter and height) of the lesion, measured with slide calipersTimepoint: Baseline, every month, up to 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| MWS- Mayo Wrist ScoreTimepoint: Baseline, every month, up to 6 months;MYMOP-2- Measure Yourself Medical Outcome ProfileTimepoint: Baseline, every month, up to 6 months;PRWE- Patient-Rated Wrist EvaluationTimepoint: Baseline, every month, up to 6 months | — |
Countries
India
Contacts
D. N. De Homoeopathic Medical College and Hospital