Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Pre-administration of 50ml or 100 ml 6% hydroxyethyl starch: Study participants will be randomized into three groups. Intervention group receiving either 50ml 6% hydroxyethyl starch or
Sponsors
Antony Xavier
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients of age group 18 to 60 years. (Dose adjustment of hydroxyethyl starch needed in paediatric and >60 years of age) 2. Patients of American Society of Anaesthesiologists (ASA) physical grade I or II.
Exclusion criteria
Exclusion criteria: 1. Patients with neurological deficits. 2. Patients with history of allergy 6% hydroxy ethyl starch and propofol. 3. Patients taking any analgesic before surgery. 4. Patients with diabetes, hypertension, cardiac disease, hepatic, renal, pulmonary disease and convulsion. 5. Patients with morbid obesity. 6. Patients with anticipated difficult venous access. 7. Patients with pregnancy and breastfeeding. 8. Patients with chronic pain syndromes. 9. Patients with disorders of lipid metabolism. 10. Patients having problems in communication.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain on propofol injectionTimepoint: Outcome will be assessed at the point of administration of propofol. Data will be then assessed at the end of one year. | — |
Secondary
| Measure | Time frame |
|---|---|
| NILTimepoint: NIL | — |
Countries
India
Contacts
Public ContactRupendra Singh Thokchom
Regional Institute of Medical Sciences, Imphal, Manipur
Outcome results
None listed