Effect of Lidocaine Pretreatment on Propofol Injection Pain During Upper Gastrointestinal Endoscopy

Effect of Lidocaine Pretreatment on Propofol Injection Pain During Upper Gastrointestinal Endoscopy: Randomized, double blind, single center study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0000045

Enrollment

Registered

2010-10-11

Start date

2009-06-26

Completion date

Unknown

Last updated

2019-03-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Drug : Patients were randomly allocated to 2 groups according to a computerized table before entering the endoscopy room: those who received lidocaine 20 mg (the lidocaine group) and those who receive

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients, 16 - 80 year-old, scheduled to undergo sedative diagnostic upper GI endoscopy

Exclusion criteria

Exclusion criteria: (1) those who were pregnant, (2) those who were allergic to soybeans, eggs or any drugs, (3) those who received sedatives or analgesics within 24 hours before the procedure, (4) those with poor general condition who had an American Society of Anesthesiology classification = 3 and (5) those who had psychiatric disorders or arrhythmia (6) those who had invisible dorsal hand vein for cannulation

Design outcomes

Primary

Measure	Time frame
pain score (severity of pain perception)	—

Secondary

Measure	Time frame
remembrance of pain	—

Countries

Korea, Republic of

Contacts

Public ContactEun Soo Kim

Keimyung University

Outcome results