Health Condition 1: O- Medical and Surgical
Conditions
Interventions
Intervention1: 2% Lignocaine: 2 % topical lignocaine used as spray prior to intradermal lignocaine anaesthesia
Control Intervention1: normal saline: 0.9 % Normal saline used as spray
Sponsors
Christian medical college
Eligibility
Inclusion criteria
Inclusion criteria: Consecutive patients undergoing respiratory diagnostic and therapeutic procedures requiring administration of intradermal ligniocaine injection and Image guided diagnostic and therapeutic pleurocentesis ,Chest drain insertion, medical Image guided closed pleural biopsy thoracoscopy during study period will be considered eligible for inclusion if they are 1.Aged above 18 years 2.Hemodynamically stable
Exclusion criteria
Exclusion criteria: 1.No consent 2.Documented history of lignocaine toxicity 3.Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the pain scores during intradermal lidocaine infiltration between two study groups i.e. 2%lidocaine spray vs Normal saline spray by using FACES score.Timepoint: Baseline | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. To compare the percentage of proportion of patients in each arm who required 2nd or more additional dose of local anesthesia to complete the procedure 2.To determine pain related adverse events(vasovagal syncope )Timepoint: baseline | — |
Countries
India
Contacts
Public ContactSobankumar
Christian medical college and hospital
Outcome results
None listed