Timing of Rocuronium After Induction With Propofol on Temporal Summation

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Clinical Trial Summary

Temporal summation of pain, which is defined as the perception of increasingly greater pain evoked by repetitive painful stimuli, is highly variable between individuals. This study aimed to determine the impact of the timing of rocuronium after induction with propofol on temporal summation of pain in gynecologic laparoscopic surgery.

See also
	Status	Clinical Trial	Phase
	Completed	`NCT04635514` - Lateral Vaginal Wall Site-specific Defect Reconstructions

NCT number	NCT04547608
Study type	Interventional
Source	Wonkwang University Hospital
Contact
Status	Completed
Phase	N/A
Start date	May 1, 2020
Completion date	September 4, 2020

Timing of Rocuronium After Induction With Propofol on Temporal Summation of Pain

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms