Comparing Lidocaine Nasal Drop and Placebo for Decrease Discomfort and Complication of Nasogastric Tube Insertion in Thammasat University Hospital: A Randomized Controlled Trial Study
Phase 1
Completed
- Conditions
- Discomfort and Complication of Nasogastric Tube InsertionNasogastric tube insertion, Lidocaine nasal drop
- Registration Number
- TCTR20230704004
- Lead Sponsor
- Faculty of medicine, Thammasat University, Pathumthani, Thailand
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 126
Inclusion Criteria
Patients who were more than 18 years old and indicated for nasogastric tube insertion (Gastrointestinal bleeding, Gastrointestinal obstruction, Enteral feeding, Severe vomitting, Post operative status)
Exclusion Criteria
[Patients who were the inability to answer questions due to alteration of consciousness or language problems, Patients who were the anatomical defects from ear/nose/throat regions that might cause difficulty in NG insertion, Patients who were signs and symptoms of coagulopathy, Patients who were history of lidocaine allergy, Patients with unstable hemodynamics due to Systolic blood pressure (< 90 mmHg) or Pulse rate (> 120/min) or Respiratory rate (> 30/min), Patients who were intoxicated]
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain score At 10 minutes after end of the intervention Visual analog scale
- Secondary Outcome Measures
Name Time Method Duration of procedure , The successful insertion , Complications At end of the intervention Record by case record form