Complex regional pain syndrome I. Complex regional pain syndrome I (CRPS I)
Conditions
Interventions
Intervention 1: Intervention group: Intervention group: they will receive 500 mg of Brand Life tablets before NPO and daily from the day after surgery for 40 days. Intervention 2: Intervention group:
Sponsors
Mazandaran University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Having informed consent Full consciousness of the patient Class 1 and 2 of the American Society of Anesthesiology Age over 18 years
Exclusion criteria
Exclusion criteria: Patients undergoing emergency surgeries Diabetes Smoking Drug use Anti-anxiety and sedative drugs Mental problems Infection before or after surgery History of allergy to vitamin C or Damask rose Patients with respiratory disorders that smell Damask rose causes worsening of respiratory condition Fibromyalgia History of carpal tunnel syndrome Previous history of complex regional pain syndrome History of previous organ surgery
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Complex regional pain syndrome I. Timepoint: 2, 4 and 6 weeks after surgery. Method of measurement: Budapest criteria. | — |
Secondary
| Measure | Time frame |
|---|---|
| Anxiety. Timepoint: Before surgery, discharge time. Method of measurement: Spielberger anxiety questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMalihe Ranjbar Moghaddam
Mazandaran University of Medical Sciences
Outcome results
None listed