Health Condition 1: T148- Other injury of unspecified body region Health Condition 2: S809- Unspecified superficial injury ofknee and lower leg Health Condition 3: S999- Unspecified injury of ankle and foot Health Condition 4: S635- Other and unspecified sprain of wrist Health Condition 5: S934- Sprain of ankle Health Condition 6: S439- Sprain of unspecified parts of shoulder girdle Health Condition 7: S534- Sprain of elbow Health Condition 8: S300- Contusion of lower back and pelvis Health Cond
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Adult participants aged 18 to 75 years. 2.Confirmed diagnosis of painful traumatic injury. - Include participants with injuries classified as AIS 1 Minor and AIS 2 Moderate. 3.Ability to provide informed consent. 4.Individuals with Apparently steady vitals and health status 5.No known allergies or adverse reactions to any drug or topical medicines. 6.Adequate understanding of the study and willingness to comply with study procedures.
Exclusion criteria
Exclusion criteria: 1.Participants with injuries classified under AIS 3 (severe) and above AIS 4, AIS 5, AIS 6 2.Known case of HIV, VDRL, Hepatitis B, C or other infectious diseases 3.Subjects with contraindications for Meshasringi Gymnema sylvestre.(RETZ)R.BR. 4.History of allergies or adverse reactions to the components of Meshasringi Gymnema sylvestre.(RETZ)R.BR. Gel. 5.Serious comorbid medical conditions, skin disorders that could confound the assessment of analgesic efficacy in painful traumatic injuries. 6.Active bleeding disorders or use of anticoagulant therapy. 7.Pregnancy or lactation. 8.Inability or unwillingness to provide informed consent. 9.Unwillingness to comply with study procedures or attend follow-up visits.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Pain scores Visual Analog Scale Numeric Rating Scale 2.Inflammatory assessment changes redness warmth, swelling, tenderness 3.Range of movements Timepoint: 1.Pain scores Visual Analog Scale-Numeric Rating Scale assessed at base line, 30th minute, and 60th minute. 2.Inflammatory assessment changes such as redness warmth, swelling, tenderness will be assessed at base line and 60th minute of the application of the gels. 3.Range of movements will be assessed for the joints involved, and will be assessed at base line and 60th minute of the application using a goniometer | — |
Secondary
| Measure | Time frame |
|---|---|
| Duration of analgesia: Time period for which the analgesic effect is maintainedTimepoint: The duration of analgesic effect will be assessed by enquiring the patient regarding the same or the time will be recorded as when the patient informs when the pain score reaches the previous value | — |
Countries
India
Contacts
Parul University