Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: Benzydamine Hydrochloride Gargle: Patients will receive 15 ml of 0.15% of Benzydamine Hydrochloride 3 mins before sedation starts
Control Intervention1: Lignocaine viscous gargle: Pati
Sponsors
M S Ramaiah Medical College
Eligibility
Inclusion criteria
Inclusion criteria: ASA physical status 1,2 and 3 BMI:18-30 kg/m2
Exclusion criteria
Exclusion criteria: 1)Pregnant women 2)Patients who have contraindication to propofol administration 3)Urgent, emergent ERCPS 4)Patients with h/o allergy to propofol, lignocaine or benzydamine hydrochloride 5)Patients with h/o throat wound ,lacerations 6)Patients who are on steroids or analgesics 24 hours prior to procedure 7)Patients with COPD 8)Patients undergoing procedure longer than 90 mins
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine the cumulative propofol consumption during the ERCP procedure.Timepoint: Total propofol dose will be recorded at the end of the procedure. | — |
Secondary
| Measure | Time frame |
|---|---|
| To determine the incidence and degree of sore throat after ERCP procedure,incidence of hypotension and desaturation and recovery time.Timepoint: Assessment of sore throat will be done at 3 different times, at the 0th hour,the 2nd hour and the 4th hour post sedation. Any side effects like hypotension, desaturation, nausea, vomitting and dysphagia if occured during study period will be noted. Recovery time from the end of the procedure until the patient achieves modified Aldrete score greater than 9 | — |
Countries
India
Contacts
Public ContactDr Archana S
M S Ramaiah Medical College
Outcome results
None listed