None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Participants with an apparently healthy status with no major diseases 2. Age between 18 and 65 years 3. Participants of either sex or transgender 4. Participants providing written informed consent voluntarily
Exclusion criteria
Exclusion criteria: 1. Subjects with active or untreated malignancy or recovered from malignancy. 2. Vulnerable population – unconscious, ambulatory, too sick for consultation, differently abled, terminally or critically ill patients, mentally incompetent people. 3. Diagnosed cases of unstable mental or psychiatric illness or other uncontrolled or life-threatening illness affecting quality of life or any organ failure. 4. Pregnant and puerperal women, lactating mothers. 5. Self-reported immune-compromised state. 6. Substance abuse and/or dependence
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Intensity of injection site pain and tenderness in both groups measured using a 0-100 mm visual analogue scale (VAS)Timepoint: Day 1, day 2, day 3, day 5, day 7, then once weekly until 1 month | — |
Secondary
| Measure | Time frame |
|---|---|
| NilTimepoint: NA | — |
Countries
India
Contacts
D N De Homoeopathic Medical College and Hospital