CTRI/2024/02/063009
Recruiting
Phase 3
Comparison of efficacy and safety of Prednisolone 20 mg vs Placebo in Diabetic patients with Complex Regional Pain Syndrome of upper extremity - PPDCRPS
Professor Jayantee Kalita0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Health Condition 1: G894- Chronic pain syndrome
- Sponsor
- Professor Jayantee Kalita
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •A) Continuous pain which is disproportionate to any inciting factor.
- •B) At least one symptom in three of the four following domains.
- •1\) Sensory: hyperesthesia with or without allodynia.
- •2\) Vasomotor: Asymmetry in temperature or skin color, skin color changes of the affected limb.
- •3\) Sudomotor/edema: Presence of edema, sweating changes or sweating asymmetry.
- •4\) Motor/ trophic: Reduced range of motion or motor dysfunction with or without trophic changes of the limb.
- •C). At least one sign in \= 2 of the following domains.
- •1\) Sensory: Hyperalgesia (to pin prick) with or without allodynia (light touch, deep somatic presence or joint movements).
- •2\) Vasomotor: Evidence of temperature or skin color asymmetry, or skin color changes.
- •3\) Sudomotor/edema: edema, sweating changes or sweating asymmetry.
Exclusion Criteria
- •Patients with uncontrolled hypertension, diabetes, infection, organ
- •failure, malignancy, shoulder joint dislocation or infection, pregnancy and unwilling for consent will be excluded
Outcomes
Primary Outcomes
Not specified
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