A study to compare between two different routes of a drug called lignocaine in smooth post operative recovery after general anaesthesia.
Not yet recruiting
- Conditions
- Medical and Surgical,
- Registration Number
- CTRI/2023/03/050634
- Lead Sponsor
- Tuba Tufail
- Brief Summary
It is a prospective double blinded trial to compare the efficacy of two different routes of the drug Lignocaine in blunting the stress response after tracheal extubation in patients undergoing general anaesthesia.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
- Patients of ASA 1 and 2 physical status.
- Patients between 16 to 60 years of age of either sex.
- Patients able to comprehend and willing to participate.
- Patients scheduled for elective surgeries under general anaesthesia.
Exclusion Criteria
- Patients refusal to participate.
- Patients with known contraindications or sensitivity to the study drug.
- Patients with pregnancy, morbid obesity and history of sore throat.
- Patients with requirement of postoperative ventilation.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Changes in Haemodynamic parameters namely Hear Rate (HR), Systolic Blood Pressure (SBP), Diastolic Blood Pressure (DBP) and Mean Arterial Pressure (MAP). Before Induction, at the time of administration of study drug, just before extubation then 1, 3, 5 and 10 minutes post extubation.
- Secondary Outcome Measures
Name Time Method Cough, sore throat, Laryngospasm. Till 2 hours Post extubation.
Trial Locations
- Locations (1)
Indira Gandhi Institute of Medical sciences
🇮🇳Patna, BIHAR, India
Indira Gandhi Institute of Medical sciences🇮🇳Patna, BIHAR, IndiaTuba TufailPrincipal investigator8677817051tubatufail@hotmail.com